TY  - JOUR
AU  - Jovanović, Jovana P.
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Minić, Aleksandra
AU  - Pejović, Anka
AU  - Katanić, Jelena
AU  - Mihailović, Vladimir B.
AU  - Nastasijević, Branislav J.
AU  - Stevanović, Dragana D.
AU  - Damljanović, Ivan S.
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7635
AB  - AlCl3-Catalyzed {[}3 + 2] dipolar cycloaddition of the N,N'-cyclic azomethine imines to the acryloylferrocene enabling access to the series of 5-substituted 6-ferrocenoyl tetrahydropyrazolo {[}1,2-a]pyrazol-1(5H)-ones. This facile methodology shows high substituent tolerance. Furthermore, easy chromatographic separations afford isolation of the pure diastereoisomers. Optimized reaction conditions, spectroscopic and electrochemical characteristics of the reaction products are provided. The X-ray structural analyses of three cycloadducts were done and obtained results were compared with properties of reported N,N'-bicyclic systems those displayed conformational similarity. Antibacterial activities of all products against two Gram-positive and two Gram-negative bacterial strains were evaluated by the experimental methods. (c) 2018 Elsevier B.V. All rights reserved.
T2  - Journal of Organometallic Chemistry
T1  - Acryloylferrocene as a convenient precursor of tetrahydropyrazolopyrazolones: [3+2] cycloaddition with N,N′ -Cyclic azomethine imines
VL  - 860
SP  - 85
EP  - 97
DO  - 10.1016/j.jorganchem.2018.02.016
ER  - 

@article{
author = "Jovanović, Jovana P. and Novaković, Slađana B. and Bogdanović, Goran A. and Minić, Aleksandra and Pejović, Anka and Katanić, Jelena and Mihailović, Vladimir B. and Nastasijević, Branislav J. and Stevanović, Dragana D. and Damljanović, Ivan S.",
year = "2018",
abstract = "AlCl3-Catalyzed {[}3 + 2] dipolar cycloaddition of the N,N'-cyclic azomethine imines to the acryloylferrocene enabling access to the series of 5-substituted 6-ferrocenoyl tetrahydropyrazolo {[}1,2-a]pyrazol-1(5H)-ones. This facile methodology shows high substituent tolerance. Furthermore, easy chromatographic separations afford isolation of the pure diastereoisomers. Optimized reaction conditions, spectroscopic and electrochemical characteristics of the reaction products are provided. The X-ray structural analyses of three cycloadducts were done and obtained results were compared with properties of reported N,N'-bicyclic systems those displayed conformational similarity. Antibacterial activities of all products against two Gram-positive and two Gram-negative bacterial strains were evaluated by the experimental methods. (c) 2018 Elsevier B.V. All rights reserved.",
journal = "Journal of Organometallic Chemistry",
title = "Acryloylferrocene as a convenient precursor of tetrahydropyrazolopyrazolones: [3+2] cycloaddition with N,N′ -Cyclic azomethine imines",
volume = "860",
pages = "85-97",
doi = "10.1016/j.jorganchem.2018.02.016"
}

Jovanović, J. P., Novaković, S. B., Bogdanović, G. A., Minić, A., Pejović, A., Katanić, J., Mihailović, V. B., Nastasijević, B. J., Stevanović, D. D.,& Damljanović, I. S.. (2018). Acryloylferrocene as a convenient precursor of tetrahydropyrazolopyrazolones: [3+2] cycloaddition with N,N′ -Cyclic azomethine imines. in Journal of Organometallic Chemistry, 860, 85-97.
https://doi.org/10.1016/j.jorganchem.2018.02.016

Jovanović JP, Novaković SB, Bogdanović GA, Minić A, Pejović A, Katanić J, Mihailović VB, Nastasijević BJ, Stevanović DD, Damljanović IS. Acryloylferrocene as a convenient precursor of tetrahydropyrazolopyrazolones: [3+2] cycloaddition with N,N′ -Cyclic azomethine imines. in Journal of Organometallic Chemistry. 2018;860:85-97.
doi:10.1016/j.jorganchem.2018.02.016 .

Jovanović, Jovana P., Novaković, Slađana B., Bogdanović, Goran A., Minić, Aleksandra, Pejović, Anka, Katanić, Jelena, Mihailović, Vladimir B., Nastasijević, Branislav J., Stevanović, Dragana D., Damljanović, Ivan S., "Acryloylferrocene as a convenient precursor of tetrahydropyrazolopyrazolones: [3+2] cycloaddition with N,N′ -Cyclic azomethine imines" in Journal of Organometallic Chemistry, 860 (2018):85-97,
https://doi.org/10.1016/j.jorganchem.2018.02.016 . .

TY  - JOUR
AU  - Bugarinović, Jovana P.
AU  - Pešić, Marko S.
AU  - Minić, Aleksandra
AU  - Katanić, Jelena
AU  - Ilić-Komatina, Danijela
AU  - Pejović, Anka
AU  - Mihailović, Vladimir B.
AU  - Stevanović, Dragana D.
AU  - Nastasijević, Branislav J.
AU  - Damljanović, Ivan S.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0162013418302472
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7890
AB  - A series of ferrocenes which contain dinitrogen-fused pyrazolidinone ring were synthesized from acryloylferrocene (4) and N,N′‑cyclic azomethine imines (3). Novel 5‑aryl‑6‑ferrocenoyltetrahydropyrazolo[1,2‑a]pyrazol‑1(5H)-ones were obtained as mixtures of two diastereoisomers (trans and cis) which were separated and isolated as pure substances. Ortho-substituted N,N′‑cyclic azomethine imines 5-oxo-2-(2,4,6-trimethylbenzylidene)pyrazolidin-2-ium-1-ide (3e) and 2-(2-methoxybenzylidene)-5-oxopyrazolidin-2-ium-1-ide (3f) reacted stereoselectively affording only trans-6-ferrocenoyl-5-mesityltetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (5e) and 6-ferrocenoyl-5-(2-methoxyphenyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (5f). Ferrocenyl derivatives were screened for in vitro antioxidant and antifungal activities and excellent DPPH and ABTS radicals scavenging activity was observed with majority of tested 5‑aryl‑6‑ferrocenoyltetrahydropyrazolo[1,2‑a]pyrazol‑1(5H)-ones. Several tested compounds showed selective scavenging properties neutralizing ABTS•+ radical cations in contrast to inactivity toward DPPH[rad] radicals. Trans-5-aryl-6-ferrocenoyltetrahydropyrazolo[1,2-a]pyrazol-1(5H)-ones 5b, 5c, 5d, 5j as well as cis-6-ferrocenoyl-5-(p-tolyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6d) displayed fungal growth inhibition at low concentration against C. albicans and/or A. brasiliensis. Molecular docking studies revealed that the cis-6-ferrocenoyl-5-(4-nitrophenyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6l) and cis-6-ferrocenoyl-5-(naphthalen-2-yl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6n) have potential to become lead molecules in drug discovery process. © 2018 Elsevier Inc.
T2  - Journal of Inorganic Biochemistry
T1  - Ferrocene-containing tetrahydropyrazolopyrazolones: Antioxidant and antimicrobial activity
VL  - 189
SP  - 134
EP  - 142
DO  - 10.1016/j.jinorgbio.2018.09.015
ER  - 

@article{
author = "Bugarinović, Jovana P. and Pešić, Marko S. and Minić, Aleksandra and Katanić, Jelena and Ilić-Komatina, Danijela and Pejović, Anka and Mihailović, Vladimir B. and Stevanović, Dragana D. and Nastasijević, Branislav J. and Damljanović, Ivan S.",
year = "2018",
abstract = "A series of ferrocenes which contain dinitrogen-fused pyrazolidinone ring were synthesized from acryloylferrocene (4) and N,N′‑cyclic azomethine imines (3). Novel 5‑aryl‑6‑ferrocenoyltetrahydropyrazolo[1,2‑a]pyrazol‑1(5H)-ones were obtained as mixtures of two diastereoisomers (trans and cis) which were separated and isolated as pure substances. Ortho-substituted N,N′‑cyclic azomethine imines 5-oxo-2-(2,4,6-trimethylbenzylidene)pyrazolidin-2-ium-1-ide (3e) and 2-(2-methoxybenzylidene)-5-oxopyrazolidin-2-ium-1-ide (3f) reacted stereoselectively affording only trans-6-ferrocenoyl-5-mesityltetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (5e) and 6-ferrocenoyl-5-(2-methoxyphenyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (5f). Ferrocenyl derivatives were screened for in vitro antioxidant and antifungal activities and excellent DPPH and ABTS radicals scavenging activity was observed with majority of tested 5‑aryl‑6‑ferrocenoyltetrahydropyrazolo[1,2‑a]pyrazol‑1(5H)-ones. Several tested compounds showed selective scavenging properties neutralizing ABTS•+ radical cations in contrast to inactivity toward DPPH[rad] radicals. Trans-5-aryl-6-ferrocenoyltetrahydropyrazolo[1,2-a]pyrazol-1(5H)-ones 5b, 5c, 5d, 5j as well as cis-6-ferrocenoyl-5-(p-tolyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6d) displayed fungal growth inhibition at low concentration against C. albicans and/or A. brasiliensis. Molecular docking studies revealed that the cis-6-ferrocenoyl-5-(4-nitrophenyl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6l) and cis-6-ferrocenoyl-5-(naphthalen-2-yl)tetrahydropyrazolo[1,2-a]pyrazol-1(5H)-one (6n) have potential to become lead molecules in drug discovery process. © 2018 Elsevier Inc.",
journal = "Journal of Inorganic Biochemistry",
title = "Ferrocene-containing tetrahydropyrazolopyrazolones: Antioxidant and antimicrobial activity",
volume = "189",
pages = "134-142",
doi = "10.1016/j.jinorgbio.2018.09.015"
}

Bugarinović, J. P., Pešić, M. S., Minić, A., Katanić, J., Ilić-Komatina, D., Pejović, A., Mihailović, V. B., Stevanović, D. D., Nastasijević, B. J.,& Damljanović, I. S.. (2018). Ferrocene-containing tetrahydropyrazolopyrazolones: Antioxidant and antimicrobial activity. in Journal of Inorganic Biochemistry, 189, 134-142.
https://doi.org/10.1016/j.jinorgbio.2018.09.015

Bugarinović JP, Pešić MS, Minić A, Katanić J, Ilić-Komatina D, Pejović A, Mihailović VB, Stevanović DD, Nastasijević BJ, Damljanović IS. Ferrocene-containing tetrahydropyrazolopyrazolones: Antioxidant and antimicrobial activity. in Journal of Inorganic Biochemistry. 2018;189:134-142.
doi:10.1016/j.jinorgbio.2018.09.015 .

Bugarinović, Jovana P., Pešić, Marko S., Minić, Aleksandra, Katanić, Jelena, Ilić-Komatina, Danijela, Pejović, Anka, Mihailović, Vladimir B., Stevanović, Dragana D., Nastasijević, Branislav J., Damljanović, Ivan S., "Ferrocene-containing tetrahydropyrazolopyrazolones: Antioxidant and antimicrobial activity" in Journal of Inorganic Biochemistry, 189 (2018):134-142,
https://doi.org/10.1016/j.jinorgbio.2018.09.015 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Minić, Aleksandra
AU  - Jovanović, Jovana P.
AU  - Pešić, Marko S.
AU  - Ilić-Komatina, Danijela
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Mihailović, Vladimir B.
AU  - Katanić, Jelena
AU  - Bogdanović, Goran A.
PY  - 2018
UR  - http://linkinghub.elsevier.com/retrieve/pii/S0022328X18303796
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7701
AB  - Synthesis of twenty novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones has been achieved in good to excellent yields by the Knoevenagel condensation of 2-ferrocenyl-1,3-thiazolidin-4-ones with aromatic aldehydes. The reaction was performed by refluxing the mixture of reactants and potassium tert-butoxide in dioxane overnight. All new compounds were characterized by the IR and NMR spectral data, and their electrochemical properties were investigated using the cyclic voltammetry. The X-ray crystal structure of one of the representative thiazolidin-4(1H)-ones is also presented. All obtained products were evaluated for their in vitro antioxidant, antibacterial and antifungal activity.
T2  - Journal of Organometallic Chemistry
T1  - Synthesis, characterization, antioxidant and antimicrobial activity of novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones
VL  - 869
SP  - 1
EP  - 10
DO  - 10.1016/j.jorganchem.2018.05.014
ER  - 

@article{
author = "Pejović, Anka and Minić, Aleksandra and Jovanović, Jovana P. and Pešić, Marko S. and Ilić-Komatina, Danijela and Damljanović, Ivan S. and Stevanović, Dragana D. and Mihailović, Vladimir B. and Katanić, Jelena and Bogdanović, Goran A.",
year = "2018",
abstract = "Synthesis of twenty novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones has been achieved in good to excellent yields by the Knoevenagel condensation of 2-ferrocenyl-1,3-thiazolidin-4-ones with aromatic aldehydes. The reaction was performed by refluxing the mixture of reactants and potassium tert-butoxide in dioxane overnight. All new compounds were characterized by the IR and NMR spectral data, and their electrochemical properties were investigated using the cyclic voltammetry. The X-ray crystal structure of one of the representative thiazolidin-4(1H)-ones is also presented. All obtained products were evaluated for their in vitro antioxidant, antibacterial and antifungal activity.",
journal = "Journal of Organometallic Chemistry",
title = "Synthesis, characterization, antioxidant and antimicrobial activity of novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones",
volume = "869",
pages = "1-10",
doi = "10.1016/j.jorganchem.2018.05.014"
}

Pejović, A., Minić, A., Jovanović, J. P., Pešić, M. S., Ilić-Komatina, D., Damljanović, I. S., Stevanović, D. D., Mihailović, V. B., Katanić, J.,& Bogdanović, G. A.. (2018). Synthesis, characterization, antioxidant and antimicrobial activity of novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones. in Journal of Organometallic Chemistry, 869, 1-10.
https://doi.org/10.1016/j.jorganchem.2018.05.014

Pejović A, Minić A, Jovanović JP, Pešić MS, Ilić-Komatina D, Damljanović IS, Stevanović DD, Mihailović VB, Katanić J, Bogdanović GA. Synthesis, characterization, antioxidant and antimicrobial activity of novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones. in Journal of Organometallic Chemistry. 2018;869:1-10.
doi:10.1016/j.jorganchem.2018.05.014 .

Pejović, Anka, Minić, Aleksandra, Jovanović, Jovana P., Pešić, Marko S., Ilić-Komatina, Danijela, Damljanović, Ivan S., Stevanović, Dragana D., Mihailović, Vladimir B., Katanić, Jelena, Bogdanović, Goran A., "Synthesis, characterization, antioxidant and antimicrobial activity of novel 5-arylidene-2-ferrocenyl-1,3-thiazolidin-4-ones" in Journal of Organometallic Chemistry, 869 (2018):1-10,
https://doi.org/10.1016/j.jorganchem.2018.05.014 . .

TY  - JOUR
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7583
AB  - Twenty-two novel 1,3-ketourea derivatives bearing ferrocene moiety were synthesized in good-to-excellent yields (up to 99%) via simple and efficient protocol. This solvent- and catalyst-free synthesis was achieved by additions of different ferrocene-containing Mannich bases - 3-(arylamino)-1-ferrocenyl-propan-1-ones to phenyl isocyanate promoted only by ultrasound irradiations at ambient temperature. All synthesized 1-aryl-3-phenyl-1-(3-ferrocenyl-3-oxopropyl)ureas were characterized by standard spectral data (H-1 NMR, C-13 NMR and IR), and their electrochemical behavior were investigated by cyclic voltammetry. Detailed single-crystal X-ray diffraction analysis of three representative ferrocene-containing 1,3-ketoureas, among which one crystallized with two independent molecules in an asymmetric unit, were done. (C) 2017 Elsevier Ltd. All rights reserved.
T2  - Polyhedron
T1  - Synthesis, structural and electrochemical characterization of novel 1,3-ketoureas bearing a ferrocenyl group
VL  - 141
SP  - 343
EP  - 351
DO  - 10.1016/j.poly.2017.12.018
ER  - 

@article{
year = "2018",
abstract = "Twenty-two novel 1,3-ketourea derivatives bearing ferrocene moiety were synthesized in good-to-excellent yields (up to 99%) via simple and efficient protocol. This solvent- and catalyst-free synthesis was achieved by additions of different ferrocene-containing Mannich bases - 3-(arylamino)-1-ferrocenyl-propan-1-ones to phenyl isocyanate promoted only by ultrasound irradiations at ambient temperature. All synthesized 1-aryl-3-phenyl-1-(3-ferrocenyl-3-oxopropyl)ureas were characterized by standard spectral data (H-1 NMR, C-13 NMR and IR), and their electrochemical behavior were investigated by cyclic voltammetry. Detailed single-crystal X-ray diffraction analysis of three representative ferrocene-containing 1,3-ketoureas, among which one crystallized with two independent molecules in an asymmetric unit, were done. (C) 2017 Elsevier Ltd. All rights reserved.",
journal = "Polyhedron",
title = "Synthesis, structural and electrochemical characterization of novel 1,3-ketoureas bearing a ferrocenyl group",
volume = "141",
pages = "343-351",
doi = "10.1016/j.poly.2017.12.018"
}

(2018). Synthesis, structural and electrochemical characterization of novel 1,3-ketoureas bearing a ferrocenyl group. in Polyhedron, 141, 343-351.
https://doi.org/10.1016/j.poly.2017.12.018

Synthesis, structural and electrochemical characterization of novel 1,3-ketoureas bearing a ferrocenyl group. in Polyhedron. 2018;141:343-351.
doi:10.1016/j.poly.2017.12.018 .

"Synthesis, structural and electrochemical characterization of novel 1,3-ketoureas bearing a ferrocenyl group" in Polyhedron, 141 (2018):343-351,
https://doi.org/10.1016/j.poly.2017.12.018 . .

TY  - JOUR
AU  - Minić, Aleksandra
AU  - Bugarinović, Jovana P.
AU  - Pejović, Anka
AU  - Ilić-Komatina, Danijela
AU  - Bogdanović, Goran A.
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0040403918310189
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7845
AB  - A simple one-pot synthesis of new ferrocene-containing 1,3-thiazinan-2-imines from 3-arylamino-1-ferrocenylpropan-1-ols and phenyl isothiocyanate has been developed. The key intermediate β-hydroxy thioureas were generated in situ using ultrasound irradiation and subsequent cyclization was achieved by the addition of acetic acid. The scope of the reaction towards various 3-arylamino-1-ferrocenylpropan-1-ols has been explored and the corresponding 3-aryl-6-ferrocenyl-N-phenyl-1,3-thiazinan-2-imines were obtained in moderate to high yields (52–90%).
T2  - Tetrahedron Letters
T1  - Synthesis of novel ferrocene-containing 1,3-thiazinan-2-imines: One-pot reaction promoted by ultrasound irradiation
VL  - 59
IS  - 38
SP  - 3499
EP  - 3502
DO  - 10.1016/j.tetlet.2018.08.029
ER  - 

@article{
author = "Minić, Aleksandra and Bugarinović, Jovana P. and Pejović, Anka and Ilić-Komatina, Danijela and Bogdanović, Goran A. and Damljanović, Ivan S. and Stevanović, Dragana D.",
year = "2018",
abstract = "A simple one-pot synthesis of new ferrocene-containing 1,3-thiazinan-2-imines from 3-arylamino-1-ferrocenylpropan-1-ols and phenyl isothiocyanate has been developed. The key intermediate β-hydroxy thioureas were generated in situ using ultrasound irradiation and subsequent cyclization was achieved by the addition of acetic acid. The scope of the reaction towards various 3-arylamino-1-ferrocenylpropan-1-ols has been explored and the corresponding 3-aryl-6-ferrocenyl-N-phenyl-1,3-thiazinan-2-imines were obtained in moderate to high yields (52–90%).",
journal = "Tetrahedron Letters",
title = "Synthesis of novel ferrocene-containing 1,3-thiazinan-2-imines: One-pot reaction promoted by ultrasound irradiation",
volume = "59",
number = "38",
pages = "3499-3502",
doi = "10.1016/j.tetlet.2018.08.029"
}

Minić, A., Bugarinović, J. P., Pejović, A., Ilić-Komatina, D., Bogdanović, G. A., Damljanović, I. S.,& Stevanović, D. D.. (2018). Synthesis of novel ferrocene-containing 1,3-thiazinan-2-imines: One-pot reaction promoted by ultrasound irradiation. in Tetrahedron Letters, 59(38), 3499-3502.
https://doi.org/10.1016/j.tetlet.2018.08.029

Minić A, Bugarinović JP, Pejović A, Ilić-Komatina D, Bogdanović GA, Damljanović IS, Stevanović DD. Synthesis of novel ferrocene-containing 1,3-thiazinan-2-imines: One-pot reaction promoted by ultrasound irradiation. in Tetrahedron Letters. 2018;59(38):3499-3502.
doi:10.1016/j.tetlet.2018.08.029 .

Minić, Aleksandra, Bugarinović, Jovana P., Pejović, Anka, Ilić-Komatina, Danijela, Bogdanović, Goran A., Damljanović, Ivan S., Stevanović, Dragana D., "Synthesis of novel ferrocene-containing 1,3-thiazinan-2-imines: One-pot reaction promoted by ultrasound irradiation" in Tetrahedron Letters, 59, no. 38 (2018):3499-3502,
https://doi.org/10.1016/j.tetlet.2018.08.029 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Minić, Aleksandra
AU  - Bugarinović, Jovana P.
AU  - Pešić, Marko S.
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Mihailović, Vladimir B.
AU  - Katanić, Jelena
AU  - Bogdanović, Goran A.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0277538718305394
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7884
AB  - A new series of ferrocene-containing thiazolylpyrazoles – 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones have been synthesized using convenient one-pot three component condensation. Twelve newly synthesized compounds were fully characterized by spectroscopic (IR and NMR) and electrochemical methods (cyclic voltammetry). Single crystal X-ray structure analysis were undertaken on two compounds. The twelve novel ferrocene derivatives were also evaluated for antimicrobial activity. The results showed moderate antimicrobial activity of synthesized compounds with better effect on Candida albicans and Gram-negative bacteria than Gram-positive bacterial strains. © 2018 Elsevier Ltd
T2  - Polyhedron
T1  - Synthesis, characterization and antimicrobial activity of novel 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones
VL  - 155
SP  - 382
EP  - 389
DO  - 10.1016/j.poly.2018.08.071
ER  - 

@article{
author = "Pejović, Anka and Minić, Aleksandra and Bugarinović, Jovana P. and Pešić, Marko S. and Damljanović, Ivan S. and Stevanović, Dragana D. and Mihailović, Vladimir B. and Katanić, Jelena and Bogdanović, Goran A.",
year = "2018",
abstract = "A new series of ferrocene-containing thiazolylpyrazoles – 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones have been synthesized using convenient one-pot three component condensation. Twelve newly synthesized compounds were fully characterized by spectroscopic (IR and NMR) and electrochemical methods (cyclic voltammetry). Single crystal X-ray structure analysis were undertaken on two compounds. The twelve novel ferrocene derivatives were also evaluated for antimicrobial activity. The results showed moderate antimicrobial activity of synthesized compounds with better effect on Candida albicans and Gram-negative bacteria than Gram-positive bacterial strains. © 2018 Elsevier Ltd",
journal = "Polyhedron",
title = "Synthesis, characterization and antimicrobial activity of novel 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones",
volume = "155",
pages = "382-389",
doi = "10.1016/j.poly.2018.08.071"
}

Pejović, A., Minić, A., Bugarinović, J. P., Pešić, M. S., Damljanović, I. S., Stevanović, D. D., Mihailović, V. B., Katanić, J.,& Bogdanović, G. A.. (2018). Synthesis, characterization and antimicrobial activity of novel 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones. in Polyhedron, 155, 382-389.
https://doi.org/10.1016/j.poly.2018.08.071

Pejović A, Minić A, Bugarinović JP, Pešić MS, Damljanović IS, Stevanović DD, Mihailović VB, Katanić J, Bogdanović GA. Synthesis, characterization and antimicrobial activity of novel 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones. in Polyhedron. 2018;155:382-389.
doi:10.1016/j.poly.2018.08.071 .

Pejović, Anka, Minić, Aleksandra, Bugarinović, Jovana P., Pešić, Marko S., Damljanović, Ivan S., Stevanović, Dragana D., Mihailović, Vladimir B., Katanić, Jelena, Bogdanović, Goran A., "Synthesis, characterization and antimicrobial activity of novel 3-ferrocenyl-2-pyrazolyl-1,3-thiazolidin-4-ones" in Polyhedron, 155 (2018):382-389,
https://doi.org/10.1016/j.poly.2018.08.071 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Minić, Aleksandra
AU  - Jovanović, Jovana P.
AU  - Mihailović, Vladimir B.
AU  - Katanić, Jelena
AU  - Bogdanović, Goran A.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1686
AB  - A three new series of the ferrocene containing quinolines - 2-ferrocenyl-4-methoxyquinolines, 1benzyl- 2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones - were synthesized in order to test their in vitro antimicrobial activity against six strains of bacteria and one fungal/yeast strain. It has been shown that all 21 quinolines are completely inactive against the Gram-positive bacteria at tested dose, while their activities on the other strains were noteworthy. All new compounds were characterized by the IR and NMR spectral data, and their electrochemical properties were investigated by the cyclic voltammetry. The X-ray crystal structure of one of the representative quinolin-4(1H)-ones is also presented. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Journal of Organometallic Chemistry
T1  - Synthesis, characterization and antimicrobial activity of novel ferrocene containing quinolines: 2-ferrocenyl-4-methoxyquinolines, 1-benzyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones
VL  - 846
SP  - 6
EP  - 17
DO  - 10.1016/j.jorganchem.2017.05.051
ER  - 

@article{
author = "Pejović, Anka and Damljanović, Ivan S. and Stevanović, Dragana D. and Minić, Aleksandra and Jovanović, Jovana P. and Mihailović, Vladimir B. and Katanić, Jelena and Bogdanović, Goran A.",
year = "2017",
abstract = "A three new series of the ferrocene containing quinolines - 2-ferrocenyl-4-methoxyquinolines, 1benzyl- 2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones - were synthesized in order to test their in vitro antimicrobial activity against six strains of bacteria and one fungal/yeast strain. It has been shown that all 21 quinolines are completely inactive against the Gram-positive bacteria at tested dose, while their activities on the other strains were noteworthy. All new compounds were characterized by the IR and NMR spectral data, and their electrochemical properties were investigated by the cyclic voltammetry. The X-ray crystal structure of one of the representative quinolin-4(1H)-ones is also presented. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Journal of Organometallic Chemistry",
title = "Synthesis, characterization and antimicrobial activity of novel ferrocene containing quinolines: 2-ferrocenyl-4-methoxyquinolines, 1-benzyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones",
volume = "846",
pages = "6-17",
doi = "10.1016/j.jorganchem.2017.05.051"
}

Pejović, A., Damljanović, I. S., Stevanović, D. D., Minić, A., Jovanović, J. P., Mihailović, V. B., Katanić, J.,& Bogdanović, G. A.. (2017). Synthesis, characterization and antimicrobial activity of novel ferrocene containing quinolines: 2-ferrocenyl-4-methoxyquinolines, 1-benzyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones. in Journal of Organometallic Chemistry, 846, 6-17.
https://doi.org/10.1016/j.jorganchem.2017.05.051

Pejović A, Damljanović IS, Stevanović DD, Minić A, Jovanović JP, Mihailović VB, Katanić J, Bogdanović GA. Synthesis, characterization and antimicrobial activity of novel ferrocene containing quinolines: 2-ferrocenyl-4-methoxyquinolines, 1-benzyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones. in Journal of Organometallic Chemistry. 2017;846:6-17.
doi:10.1016/j.jorganchem.2017.05.051 .

Pejović, Anka, Damljanović, Ivan S., Stevanović, Dragana D., Minić, Aleksandra, Jovanović, Jovana P., Mihailović, Vladimir B., Katanić, Jelena, Bogdanović, Goran A., "Synthesis, characterization and antimicrobial activity of novel ferrocene containing quinolines: 2-ferrocenyl-4-methoxyquinolines, 1-benzyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-benzyl-2-ferrocenylquinolin-4(1H)-ones" in Journal of Organometallic Chemistry, 846 (2017):6-17,
https://doi.org/10.1016/j.jorganchem.2017.05.051 . .

TY  - JOUR
AU  - Stevanović, Dragana D.
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Minić, Aleksandra
AU  - Bogdanović, Goran A.
AU  - Vukićević, Mirjana
AU  - Radulović, Niko S.
AU  - Vukićević, Rastko D.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/489
AB  - In situ generated zirconium catalyst from a sacrificial zirconium anode was successfully applied to promote Ferrier rearrangement of 3,4,5-tri-O-acetyl-D-glucal and 6-deoxy-3,4-di-O-acetyl-L-glucal (3,4-di- O-acetyl-L-rhamnal) in the presence of three thiols and eleven thiophenols as nucleophiles. A simple constant current electrolysis (20 mA, 0.4 F mol(-1)) of an acetonitrile solution of lithium perchlorate (0.1 M) containing the corresponding glycal and S-nucleophiles, using a zirconium anode and a platinum cathode resulted in the successful synthesis of the corresponding 2,3-unsaturated peracetylated thioglycosides (with an average anomer ratio alpha/beta-4.129 in the case of peracetylated D-glucal and 8.740 in the case of L-rhamnal). The same procedure proved to be appropriate in synthesizing dihydropyran derivatives (C-glycosides) using allyltrimethylsilane as the nucleophile (only alpha-anomers were obtained). All new compounds were fully characterized by spectral data, whereas single-crystal X-ray analysis was performed for two thioglycosides. (C) 2015 Elsevier Ltd. All rights reserved.
T2  - Carbohydrate Research
T1  - Ferrier rearrangement promoted by an electrochemically generated zirconium catalyst
VL  - 407
SP  - 111
EP  - 121
DO  - 10.1016/j.carres.2015.02.001
ER  - 

@article{
author = "Stevanović, Dragana D. and Pejović, Anka and Damljanović, Ivan S. and Minić, Aleksandra and Bogdanović, Goran A. and Vukićević, Mirjana and Radulović, Niko S. and Vukićević, Rastko D.",
year = "2015",
abstract = "In situ generated zirconium catalyst from a sacrificial zirconium anode was successfully applied to promote Ferrier rearrangement of 3,4,5-tri-O-acetyl-D-glucal and 6-deoxy-3,4-di-O-acetyl-L-glucal (3,4-di- O-acetyl-L-rhamnal) in the presence of three thiols and eleven thiophenols as nucleophiles. A simple constant current electrolysis (20 mA, 0.4 F mol(-1)) of an acetonitrile solution of lithium perchlorate (0.1 M) containing the corresponding glycal and S-nucleophiles, using a zirconium anode and a platinum cathode resulted in the successful synthesis of the corresponding 2,3-unsaturated peracetylated thioglycosides (with an average anomer ratio alpha/beta-4.129 in the case of peracetylated D-glucal and 8.740 in the case of L-rhamnal). The same procedure proved to be appropriate in synthesizing dihydropyran derivatives (C-glycosides) using allyltrimethylsilane as the nucleophile (only alpha-anomers were obtained). All new compounds were fully characterized by spectral data, whereas single-crystal X-ray analysis was performed for two thioglycosides. (C) 2015 Elsevier Ltd. All rights reserved.",
journal = "Carbohydrate Research",
title = "Ferrier rearrangement promoted by an electrochemically generated zirconium catalyst",
volume = "407",
pages = "111-121",
doi = "10.1016/j.carres.2015.02.001"
}

Stevanović, D. D., Pejović, A., Damljanović, I. S., Minić, A., Bogdanović, G. A., Vukićević, M., Radulović, N. S.,& Vukićević, R. D.. (2015). Ferrier rearrangement promoted by an electrochemically generated zirconium catalyst. in Carbohydrate Research, 407, 111-121.
https://doi.org/10.1016/j.carres.2015.02.001

Stevanović DD, Pejović A, Damljanović IS, Minić A, Bogdanović GA, Vukićević M, Radulović NS, Vukićević RD. Ferrier rearrangement promoted by an electrochemically generated zirconium catalyst. in Carbohydrate Research. 2015;407:111-121.
doi:10.1016/j.carres.2015.02.001 .

Stevanović, Dragana D., Pejović, Anka, Damljanović, Ivan S., Minić, Aleksandra, Bogdanović, Goran A., Vukićević, Mirjana, Radulović, Niko S., Vukićević, Rastko D., "Ferrier rearrangement promoted by an electrochemically generated zirconium catalyst" in Carbohydrate Research, 407 (2015):111-121,
https://doi.org/10.1016/j.carres.2015.02.001 . .

TY  - JOUR
AU  - Minić, Aleksandra
AU  - Stevanović, Dragana D.
AU  - Damljanović, Ivan S.
AU  - Pejović, Anka
AU  - Vukićević, Mirjana
AU  - Bogdanović, Goran A.
AU  - Radulović, Niko S.
AU  - Vukićević, Rastko D.
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/456
AB  - A series of ferrocene-containing six-membered cyclic ureas (1-aryl-4-ferrocenyl-3-phenyltetrahydropyrimidin-2(1H)-ones) was synthesized (in high-to-excellent yields) by reacting the corresponding amino-propanols with phenyl isocyanate and the subsequent intramolecular cyclization of the thus obtained beta-hydroxy ureas (prompted by acetic acid), via an alpha-ferrocenyl carbocation.
T2  - RSC Advances
T1  - Synthesis of ferrocene-containing six-membered cyclic ureas via alpha-ferrocenyl carbocations
VL  - 5
IS  - 32
SP  - 24915
EP  - 24919
DO  - 10.1039/c5ra01383f
ER  - 

@article{
author = "Minić, Aleksandra and Stevanović, Dragana D. and Damljanović, Ivan S. and Pejović, Anka and Vukićević, Mirjana and Bogdanović, Goran A. and Radulović, Niko S. and Vukićević, Rastko D.",
year = "2015",
abstract = "A series of ferrocene-containing six-membered cyclic ureas (1-aryl-4-ferrocenyl-3-phenyltetrahydropyrimidin-2(1H)-ones) was synthesized (in high-to-excellent yields) by reacting the corresponding amino-propanols with phenyl isocyanate and the subsequent intramolecular cyclization of the thus obtained beta-hydroxy ureas (prompted by acetic acid), via an alpha-ferrocenyl carbocation.",
journal = "RSC Advances",
title = "Synthesis of ferrocene-containing six-membered cyclic ureas via alpha-ferrocenyl carbocations",
volume = "5",
number = "32",
pages = "24915-24919",
doi = "10.1039/c5ra01383f"
}

Minić, A., Stevanović, D. D., Damljanović, I. S., Pejović, A., Vukićević, M., Bogdanović, G. A., Radulović, N. S.,& Vukićević, R. D.. (2015). Synthesis of ferrocene-containing six-membered cyclic ureas via alpha-ferrocenyl carbocations. in RSC Advances, 5(32), 24915-24919.
https://doi.org/10.1039/c5ra01383f

Minić A, Stevanović DD, Damljanović IS, Pejović A, Vukićević M, Bogdanović GA, Radulović NS, Vukićević RD. Synthesis of ferrocene-containing six-membered cyclic ureas via alpha-ferrocenyl carbocations. in RSC Advances. 2015;5(32):24915-24919.
doi:10.1039/c5ra01383f .

Minić, Aleksandra, Stevanović, Dragana D., Damljanović, Ivan S., Pejović, Anka, Vukićević, Mirjana, Bogdanović, Goran A., Radulović, Niko S., Vukićević, Rastko D., "Synthesis of ferrocene-containing six-membered cyclic ureas via alpha-ferrocenyl carbocations" in RSC Advances, 5, no. 32 (2015):24915-24919,
https://doi.org/10.1039/c5ra01383f . .

TY  - JOUR
AU  - Stevanović, Dragana
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Vukićević, Mirjana
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Vukićević, Rastko
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11003
AB  - Michael addition of diethyl malonate, ethyl acetoacetate, acetylacetone, and cyanide anion to acryloylferrocene promoted by a catalyst in situ generated from a sacrificial zirconium anode is described. Most of the obtained compounds were identified by comparison of their spectral and physical data with those published elsewhere, whereas the only newly synthesized compound - diethyl 2,2-bis(3-ferrocenyl-3-oxopropyl)malonate - was completely characterized by spectral (IR, 1H- and 13C-NMR), physical and crystallographic (single-crystal X-ray) data.
AB  - Opisana je Majklova adicija dietil-malonata, etil-acetoacetata, acetilacetona i cijanidnog anjona na akriloilferocen pomoću katalizatora generisanog in situ sa rastvorne anode od cirkonijuma. Većina dobijenih jedinjenja je identifikovana poređenjem njihovih fizičkih i spektroskopskih podataka sa literaturnim, a jedino novo jedinjenje je potpuno opisano spektroskopskim (IR, 1H- i 13C-NMR) i fizičkim podacima, kao i podacima iz kristalografske analize X-zracima.
T2  - Facta universitatis - series: Physics, Chemistry and Technology
T1  - Electrochemical generation of a catalyst for Мichael addition of dicarbonyl compounds and cyanide anion to acryloylferrocene
T1  - Elektrohemijsko generisanje katalizatora za Majklovu adiciju dikarbonilnih jedinjenja i cijanida na akriloilferocen
VL  - 13
IS  - 2
SP  - 67
EP  - 76
DO  - 10.2298/FUPCT1502067S
ER  - 

@article{
author = "Stevanović, Dragana and Pejović, Anka and Damljanović, Ivan S. and Vukićević, Mirjana and Novaković, Slađana B. and Bogdanović, Goran A. and Vukićević, Rastko",
year = "2015",
abstract = "Michael addition of diethyl malonate, ethyl acetoacetate, acetylacetone, and cyanide anion to acryloylferrocene promoted by a catalyst in situ generated from a sacrificial zirconium anode is described. Most of the obtained compounds were identified by comparison of their spectral and physical data with those published elsewhere, whereas the only newly synthesized compound - diethyl 2,2-bis(3-ferrocenyl-3-oxopropyl)malonate - was completely characterized by spectral (IR, 1H- and 13C-NMR), physical and crystallographic (single-crystal X-ray) data., Opisana je Majklova adicija dietil-malonata, etil-acetoacetata, acetilacetona i cijanidnog anjona na akriloilferocen pomoću katalizatora generisanog in situ sa rastvorne anode od cirkonijuma. Većina dobijenih jedinjenja je identifikovana poređenjem njihovih fizičkih i spektroskopskih podataka sa literaturnim, a jedino novo jedinjenje je potpuno opisano spektroskopskim (IR, 1H- i 13C-NMR) i fizičkim podacima, kao i podacima iz kristalografske analize X-zracima.",
journal = "Facta universitatis - series: Physics, Chemistry and Technology",
title = "Electrochemical generation of a catalyst for Мichael addition of dicarbonyl compounds and cyanide anion to acryloylferrocene, Elektrohemijsko generisanje katalizatora za Majklovu adiciju dikarbonilnih jedinjenja i cijanida na akriloilferocen",
volume = "13",
number = "2",
pages = "67-76",
doi = "10.2298/FUPCT1502067S"
}

Stevanović, D., Pejović, A., Damljanović, I. S., Vukićević, M., Novaković, S. B., Bogdanović, G. A.,& Vukićević, R.. (2015). Electrochemical generation of a catalyst for Мichael addition of dicarbonyl compounds and cyanide anion to acryloylferrocene. in Facta universitatis - series: Physics, Chemistry and Technology, 13(2), 67-76.
https://doi.org/10.2298/FUPCT1502067S

Stevanović D, Pejović A, Damljanović IS, Vukićević M, Novaković SB, Bogdanović GA, Vukićević R. Electrochemical generation of a catalyst for Мichael addition of dicarbonyl compounds and cyanide anion to acryloylferrocene. in Facta universitatis - series: Physics, Chemistry and Technology. 2015;13(2):67-76.
doi:10.2298/FUPCT1502067S .

Stevanović, Dragana, Pejović, Anka, Damljanović, Ivan S., Vukićević, Mirjana, Novaković, Slađana B., Bogdanović, Goran A., Vukićević, Rastko, "Electrochemical generation of a catalyst for Мichael addition of dicarbonyl compounds and cyanide anion to acryloylferrocene" in Facta universitatis - series: Physics, Chemistry and Technology, 13, no. 2 (2015):67-76,
https://doi.org/10.2298/FUPCT1502067S . .

TY  - JOUR
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Pejović, Anka
AU  - Ilic, Danijela
AU  - Živković, Marija D.
AU  - Jovanović, Jovana P.
AU  - Vukićević, Mirjana
AU  - Bogdanović, Goran A.
AU  - Radulović, Niko S.
AU  - Vukićević, Rastko D.
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/193
AB  - In this paper we wish to present the first results on the synthesis of N, N-diethyl-1-ferrocenyl-3-thiabutanamine, its coordination with palladium(II), the complete characterization of the thus obtained complex (including single crystal X-ray analysis for the complex in two polymorphic forms) and screening of its catalytic activity in Suzuki-Miyaura coupling of phenylboronic acid with several aryl bromides. The complex, either purified and then added to the reaction mixture or generated in situ, proved to be an excellent precatalyst in Suzuki-Miyaura coupling. The chemical behavior of the complex in solution was assessed by detailed NMR analyses and cyclic voltammetry measurements which allowed us to draw a number of mechanistic conclusions.
T2  - RSC Advances
T1  - The palladium(II) complex of N,N-diethyl-1-ferrocenyl-3-thiabutanamine: synthesis, solution and solid state structure and catalytic activity in Suzuki-Miyaura reaction
VL  - 4
IS  - 82
SP  - 43792
EP  - 43799
DO  - 10.1039/c4ra08140d
ER  - 

@article{
author = "Damljanović, Ivan S. and Stevanović, Dragana D. and Pejović, Anka and Ilic, Danijela and Živković, Marija D. and Jovanović, Jovana P. and Vukićević, Mirjana and Bogdanović, Goran A. and Radulović, Niko S. and Vukićević, Rastko D.",
year = "2014",
abstract = "In this paper we wish to present the first results on the synthesis of N, N-diethyl-1-ferrocenyl-3-thiabutanamine, its coordination with palladium(II), the complete characterization of the thus obtained complex (including single crystal X-ray analysis for the complex in two polymorphic forms) and screening of its catalytic activity in Suzuki-Miyaura coupling of phenylboronic acid with several aryl bromides. The complex, either purified and then added to the reaction mixture or generated in situ, proved to be an excellent precatalyst in Suzuki-Miyaura coupling. The chemical behavior of the complex in solution was assessed by detailed NMR analyses and cyclic voltammetry measurements which allowed us to draw a number of mechanistic conclusions.",
journal = "RSC Advances",
title = "The palladium(II) complex of N,N-diethyl-1-ferrocenyl-3-thiabutanamine: synthesis, solution and solid state structure and catalytic activity in Suzuki-Miyaura reaction",
volume = "4",
number = "82",
pages = "43792-43799",
doi = "10.1039/c4ra08140d"
}

Damljanović, I. S., Stevanović, D. D., Pejović, A., Ilic, D., Živković, M. D., Jovanović, J. P., Vukićević, M., Bogdanović, G. A., Radulović, N. S.,& Vukićević, R. D.. (2014). The palladium(II) complex of N,N-diethyl-1-ferrocenyl-3-thiabutanamine: synthesis, solution and solid state structure and catalytic activity in Suzuki-Miyaura reaction. in RSC Advances, 4(82), 43792-43799.
https://doi.org/10.1039/c4ra08140d

Damljanović IS, Stevanović DD, Pejović A, Ilic D, Živković MD, Jovanović JP, Vukićević M, Bogdanović GA, Radulović NS, Vukićević RD. The palladium(II) complex of N,N-diethyl-1-ferrocenyl-3-thiabutanamine: synthesis, solution and solid state structure and catalytic activity in Suzuki-Miyaura reaction. in RSC Advances. 2014;4(82):43792-43799.
doi:10.1039/c4ra08140d .

Damljanović, Ivan S., Stevanović, Dragana D., Pejović, Anka, Ilic, Danijela, Živković, Marija D., Jovanović, Jovana P., Vukićević, Mirjana, Bogdanović, Goran A., Radulović, Niko S., Vukićević, Rastko D., "The palladium(II) complex of N,N-diethyl-1-ferrocenyl-3-thiabutanamine: synthesis, solution and solid state structure and catalytic activity in Suzuki-Miyaura reaction" in RSC Advances, 4, no. 82 (2014):43792-43799,
https://doi.org/10.1039/c4ra08140d . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Denic, Marija S.
AU  - Stevanović, Dragana D.
AU  - Damljanović, Ivan S.
AU  - Vukićević, Mirjana
AU  - Kostova, Kalina
AU  - Tavlinova-Kirilova, Maya
AU  - Randjelovi, Pavle
AU  - Stojanović, Nikola M.
AU  - Bogdanović, Goran A.
AU  - Blagojevic, Polina
AU  - D'hooghe, Matthias
AU  - Radulović, Niko S.
AU  - Vukićević, Rastko D.
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/76
AB  - Herein, we report on the synthesis, spectral, crystallographic and electrochemical properties of a small library of N-substituted 2-ferrocenyl-1,3-thiazolidin-4-ones, designed as novel GABA(A) benzodiazepine-binding site ligands. The anxiolytic properties of the title compounds were evaluated in several different in vivo models, whereas the involvement of the GABAA receptor complex in the activity of the most potent compound, 2-ferrocenyl-3-(4-methoxyphenylethyl)-1,3-thiazolidin-4-one, was inferred from experiments with known GABA(A)-targeting agents. Ligand docking experiments revealed that the high, dose-dependent, anxiolytic activity of the new compounds might be due to their favorable interactions with the benzodiazepine-binding site of the GABA(A) receptor complex. The incorporation of the ferrocene core and fine tuning of the distance between the thiazolidinone core and an additional aromatic ring were judged to be crucial structural requirements for the observed anxiolytic effect. (C) 2014 Elsevier Masson SAS. All rights reserved.
T2  - European Journal of Medicinal Chemistry
T1  - Discovery of anxiolytic 2-ferrocenyl-1,3-thiazolidin-4-ones exerting GABA(A) receptor interaction via the benzodiazepine-binding site
VL  - 83
SP  - 57
EP  - 73
DO  - 10.1016/j.ejmech.2014.05.062
ER  - 

@article{
author = "Pejović, Anka and Denic, Marija S. and Stevanović, Dragana D. and Damljanović, Ivan S. and Vukićević, Mirjana and Kostova, Kalina and Tavlinova-Kirilova, Maya and Randjelovi, Pavle and Stojanović, Nikola M. and Bogdanović, Goran A. and Blagojevic, Polina and D'hooghe, Matthias and Radulović, Niko S. and Vukićević, Rastko D.",
year = "2014",
abstract = "Herein, we report on the synthesis, spectral, crystallographic and electrochemical properties of a small library of N-substituted 2-ferrocenyl-1,3-thiazolidin-4-ones, designed as novel GABA(A) benzodiazepine-binding site ligands. The anxiolytic properties of the title compounds were evaluated in several different in vivo models, whereas the involvement of the GABAA receptor complex in the activity of the most potent compound, 2-ferrocenyl-3-(4-methoxyphenylethyl)-1,3-thiazolidin-4-one, was inferred from experiments with known GABA(A)-targeting agents. Ligand docking experiments revealed that the high, dose-dependent, anxiolytic activity of the new compounds might be due to their favorable interactions with the benzodiazepine-binding site of the GABA(A) receptor complex. The incorporation of the ferrocene core and fine tuning of the distance between the thiazolidinone core and an additional aromatic ring were judged to be crucial structural requirements for the observed anxiolytic effect. (C) 2014 Elsevier Masson SAS. All rights reserved.",
journal = "European Journal of Medicinal Chemistry",
title = "Discovery of anxiolytic 2-ferrocenyl-1,3-thiazolidin-4-ones exerting GABA(A) receptor interaction via the benzodiazepine-binding site",
volume = "83",
pages = "57-73",
doi = "10.1016/j.ejmech.2014.05.062"
}

Pejović, A., Denic, M. S., Stevanović, D. D., Damljanović, I. S., Vukićević, M., Kostova, K., Tavlinova-Kirilova, M., Randjelovi, P., Stojanović, N. M., Bogdanović, G. A., Blagojevic, P., D'hooghe, M., Radulović, N. S.,& Vukićević, R. D.. (2014). Discovery of anxiolytic 2-ferrocenyl-1,3-thiazolidin-4-ones exerting GABA(A) receptor interaction via the benzodiazepine-binding site. in European Journal of Medicinal Chemistry, 83, 57-73.
https://doi.org/10.1016/j.ejmech.2014.05.062

Pejović A, Denic MS, Stevanović DD, Damljanović IS, Vukićević M, Kostova K, Tavlinova-Kirilova M, Randjelovi P, Stojanović NM, Bogdanović GA, Blagojevic P, D'hooghe M, Radulović NS, Vukićević RD. Discovery of anxiolytic 2-ferrocenyl-1,3-thiazolidin-4-ones exerting GABA(A) receptor interaction via the benzodiazepine-binding site. in European Journal of Medicinal Chemistry. 2014;83:57-73.
doi:10.1016/j.ejmech.2014.05.062 .

Pejović, Anka, Denic, Marija S., Stevanović, Dragana D., Damljanović, Ivan S., Vukićević, Mirjana, Kostova, Kalina, Tavlinova-Kirilova, Maya, Randjelovi, Pavle, Stojanović, Nikola M., Bogdanović, Goran A., Blagojevic, Polina, D'hooghe, Matthias, Radulović, Niko S., Vukićević, Rastko D., "Discovery of anxiolytic 2-ferrocenyl-1,3-thiazolidin-4-ones exerting GABA(A) receptor interaction via the benzodiazepine-binding site" in European Journal of Medicinal Chemistry, 83 (2014):57-73,
https://doi.org/10.1016/j.ejmech.2014.05.062 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Ilic, Danijela
AU  - Vukićević, Mirjana
AU  - Bogdanović, Goran A.
AU  - Vukićević, Rastko D.
PY  - 2013
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5623
AB  - Dimethyl(2-ferrocenoylethyl)sulfonium iodide was synthesized by reacting 1-ferroceny1-4-thiapentan-1-one with iodomethane and characterized from spectral data and single crystal X-ray structure analysis. This compound was capable of reacting with different N-, S-, and O-nucleophiles giving the corresponding beta-functionalized ferrocene-containing ketones. Furthermore, dimethyl sulfide can be displaced from the dimethyl(2-ferrocenoylethyl)sulfonium ion with cyanide or carbanions derived from 1,3-bifunctional compounds and nitropropane, leading to products with a new carbon-carbon bond. (C) 2013 Elsevier Ltd. All rights reserved.
T2  - Tetrahedron Letters
T1  - Synthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide
VL  - 54
IS  - 35
SP  - 4776
EP  - 4780
DO  - 10.1016/j.tetlet.2013.06.130
ER  - 

@article{
author = "Pejović, Anka and Damljanović, Ivan S. and Stevanović, Dragana D. and Ilic, Danijela and Vukićević, Mirjana and Bogdanović, Goran A. and Vukićević, Rastko D.",
year = "2013",
abstract = "Dimethyl(2-ferrocenoylethyl)sulfonium iodide was synthesized by reacting 1-ferroceny1-4-thiapentan-1-one with iodomethane and characterized from spectral data and single crystal X-ray structure analysis. This compound was capable of reacting with different N-, S-, and O-nucleophiles giving the corresponding beta-functionalized ferrocene-containing ketones. Furthermore, dimethyl sulfide can be displaced from the dimethyl(2-ferrocenoylethyl)sulfonium ion with cyanide or carbanions derived from 1,3-bifunctional compounds and nitropropane, leading to products with a new carbon-carbon bond. (C) 2013 Elsevier Ltd. All rights reserved.",
journal = "Tetrahedron Letters",
title = "Synthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide",
volume = "54",
number = "35",
pages = "4776-4780",
doi = "10.1016/j.tetlet.2013.06.130"
}

Pejović, A., Damljanović, I. S., Stevanović, D. D., Ilic, D., Vukićević, M., Bogdanović, G. A.,& Vukićević, R. D.. (2013). Synthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide. in Tetrahedron Letters, 54(35), 4776-4780.
https://doi.org/10.1016/j.tetlet.2013.06.130

Pejović A, Damljanović IS, Stevanović DD, Ilic D, Vukićević M, Bogdanović GA, Vukićević RD. Synthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide. in Tetrahedron Letters. 2013;54(35):4776-4780.
doi:10.1016/j.tetlet.2013.06.130 .

Pejović, Anka, Damljanović, Ivan S., Stevanović, Dragana D., Ilic, Danijela, Vukićević, Mirjana, Bogdanović, Goran A., Vukićević, Rastko D., "Synthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide" in Tetrahedron Letters, 54, no. 35 (2013):4776-4780,
https://doi.org/10.1016/j.tetlet.2013.06.130 . .

TY  - JOUR
AU  - Stevanović, Dragana D.
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Vukićević, Mirjana
AU  - Bogdanović, Goran A.
AU  - Vukićević, Rastko D.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5163
AB  - An efficient catalyst for Ferrier rearrangement and hetero-Michael addition was successfully generated from a sacrificial zirconium anode into media containing reactants for these reactions. Thus, the catalyst generated, successfully promoted the allylic rearrangement of peracetylated D-glucal in the presence of a suitable S-nucleophile, giving the corresponding 2,3-unsaturated D-glucopyranose (pseudoglycal) in good to high yields. This catalyst was also shown to be capable of promoting hetero-Michael conjugate addition of S- and N-nucleophiles to the carbon-carbon double bond of methyl vinyl ketone, resulting in new carbon-sulfur and carbon-nitrogen bond formation. (C) 2012 Elsevier Ltd. All rights reserved.
T2  - Tetrahedron Letters
T1  - Anodic generation of a zirconium catalyst for Ferrier rearrangement and hetero Michael addition
VL  - 53
IS  - 46
SP  - 6257
EP  - 6260
DO  - 10.1016/j.tetlet.2012.09.023
ER  - 

@article{
author = "Stevanović, Dragana D. and Pejović, Anka and Damljanović, Ivan S. and Vukićević, Mirjana and Bogdanović, Goran A. and Vukićević, Rastko D.",
year = "2012",
abstract = "An efficient catalyst for Ferrier rearrangement and hetero-Michael addition was successfully generated from a sacrificial zirconium anode into media containing reactants for these reactions. Thus, the catalyst generated, successfully promoted the allylic rearrangement of peracetylated D-glucal in the presence of a suitable S-nucleophile, giving the corresponding 2,3-unsaturated D-glucopyranose (pseudoglycal) in good to high yields. This catalyst was also shown to be capable of promoting hetero-Michael conjugate addition of S- and N-nucleophiles to the carbon-carbon double bond of methyl vinyl ketone, resulting in new carbon-sulfur and carbon-nitrogen bond formation. (C) 2012 Elsevier Ltd. All rights reserved.",
journal = "Tetrahedron Letters",
title = "Anodic generation of a zirconium catalyst for Ferrier rearrangement and hetero Michael addition",
volume = "53",
number = "46",
pages = "6257-6260",
doi = "10.1016/j.tetlet.2012.09.023"
}

Stevanović, D. D., Pejović, A., Damljanović, I. S., Vukićević, M., Bogdanović, G. A.,& Vukićević, R. D.. (2012). Anodic generation of a zirconium catalyst for Ferrier rearrangement and hetero Michael addition. in Tetrahedron Letters, 53(46), 6257-6260.
https://doi.org/10.1016/j.tetlet.2012.09.023

Stevanović DD, Pejović A, Damljanović IS, Vukićević M, Bogdanović GA, Vukićević RD. Anodic generation of a zirconium catalyst for Ferrier rearrangement and hetero Michael addition. in Tetrahedron Letters. 2012;53(46):6257-6260.
doi:10.1016/j.tetlet.2012.09.023 .

Stevanović, Dragana D., Pejović, Anka, Damljanović, Ivan S., Vukićević, Mirjana, Bogdanović, Goran A., Vukićević, Rastko D., "Anodic generation of a zirconium catalyst for Ferrier rearrangement and hetero Michael addition" in Tetrahedron Letters, 53, no. 46 (2012):6257-6260,
https://doi.org/10.1016/j.tetlet.2012.09.023 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Stevanović, Dragana D.
AU  - Damljanović, Ivan S.
AU  - Vukićević, Mirjana
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Mihajilov-Krstev, Tatjana
AU  - Radulovic, Niko
AU  - Vukićević, Rastko D.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5014
AB  - A successful aza-Michael addition of arylamines to a conjugated enone, acryloylferrocene, has been achieved by ultrasonic irradiation of the mixture of these reactants and the catalyst, i.e., montmorillonite K-10. This solvent-free reaction, yielding ferrocene containing Mannich bases, 3-(arylamino)-1-ferrocenylpropan-1-ones, considered as valuable precursors in organic synthesis, has been performed by using a simple ultrasonic cleaner. Among 17 synthesized beta-amino ketones, three were new ones, and these were fully characterized by spectroscopic means. X-Ray crystallographic analysis of three of these crystalline products enabled the insight into the conformational details of these compounds. All compounds were evaluated for their antibacterial activities against six Gram-positive and five Gram-negative strains in a microdilution assay. The observed promising antibacterial activity (with a MIC value of 25 mu g/ml (ca. 0.07 mu mol/ml) as the best result for almost all tested compounds against Micrococcus flavus) seems not only to be compound but also bacterial species-specific.
T2  - Helvetica Chimica Acta
T1  - Ultrasound-Assisted Synthesis of 3-(Arylamino)-1-ferrocenylpropan-1-ones
VL  - 95
IS  - 8
SP  - 1425
EP  - 1441
DO  - 10.1002/hlca.201200009
ER  - 

@article{
author = "Pejović, Anka and Stevanović, Dragana D. and Damljanović, Ivan S. and Vukićević, Mirjana and Novaković, Slađana B. and Bogdanović, Goran A. and Mihajilov-Krstev, Tatjana and Radulovic, Niko and Vukićević, Rastko D.",
year = "2012",
abstract = "A successful aza-Michael addition of arylamines to a conjugated enone, acryloylferrocene, has been achieved by ultrasonic irradiation of the mixture of these reactants and the catalyst, i.e., montmorillonite K-10. This solvent-free reaction, yielding ferrocene containing Mannich bases, 3-(arylamino)-1-ferrocenylpropan-1-ones, considered as valuable precursors in organic synthesis, has been performed by using a simple ultrasonic cleaner. Among 17 synthesized beta-amino ketones, three were new ones, and these were fully characterized by spectroscopic means. X-Ray crystallographic analysis of three of these crystalline products enabled the insight into the conformational details of these compounds. All compounds were evaluated for their antibacterial activities against six Gram-positive and five Gram-negative strains in a microdilution assay. The observed promising antibacterial activity (with a MIC value of 25 mu g/ml (ca. 0.07 mu mol/ml) as the best result for almost all tested compounds against Micrococcus flavus) seems not only to be compound but also bacterial species-specific.",
journal = "Helvetica Chimica Acta",
title = "Ultrasound-Assisted Synthesis of 3-(Arylamino)-1-ferrocenylpropan-1-ones",
volume = "95",
number = "8",
pages = "1425-1441",
doi = "10.1002/hlca.201200009"
}

Pejović, A., Stevanović, D. D., Damljanović, I. S., Vukićević, M., Novaković, S. B., Bogdanović, G. A., Mihajilov-Krstev, T., Radulovic, N.,& Vukićević, R. D.. (2012). Ultrasound-Assisted Synthesis of 3-(Arylamino)-1-ferrocenylpropan-1-ones. in Helvetica Chimica Acta, 95(8), 1425-1441.
https://doi.org/10.1002/hlca.201200009

Pejović A, Stevanović DD, Damljanović IS, Vukićević M, Novaković SB, Bogdanović GA, Mihajilov-Krstev T, Radulovic N, Vukićević RD. Ultrasound-Assisted Synthesis of 3-(Arylamino)-1-ferrocenylpropan-1-ones. in Helvetica Chimica Acta. 2012;95(8):1425-1441.
doi:10.1002/hlca.201200009 .

Pejović, Anka, Stevanović, Dragana D., Damljanović, Ivan S., Vukićević, Mirjana, Novaković, Slađana B., Bogdanović, Goran A., Mihajilov-Krstev, Tatjana, Radulovic, Niko, Vukićević, Rastko D., "Ultrasound-Assisted Synthesis of 3-(Arylamino)-1-ferrocenylpropan-1-ones" in Helvetica Chimica Acta, 95, no. 8 (2012):1425-1441,
https://doi.org/10.1002/hlca.201200009 . .

TY  - JOUR
AU  - Pejović, Anka
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Vukićević, Mirjana
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Radulovic, Niko
AU  - Vukićević, Rastko D.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4710
AB  - Syntheses of three new ferrocene containing heterocycles - 2-ferroceny1-2,3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives - starting from 2-aminoacetophenones and ferrocenecarboxaldehyde was achieved in two steps. The aldol condensation of these substrates gave the corresponding 2-aminochalcones in the first stage, whereas a further intramolecular cyclization gives the final products. This cyclization was performed by either a solvent-free microwave irradiation (500 W/5 min) of a mixture of chalcones and mortmorillonite K-10 or by using an acidic catalyst (the mixture of acetic and orthophosphoric acid). The latter method, which can be performed by simple stirring at room temperature or by irradiation in an ultrasonic bath, gave much better results. The obtained compounds were spectrally and electrochemically (cyclic voltammetry) fully characterized, as well as by single-crystal X-ray analysis. A microdilution assay revealed that the three dihydroquinolinones can be regarded as potential lead compounds in the discovery of new antimicrobial drugs due to their very strong and unselective activity towards pathogenic bacteria and one yeast with MIC values (0.01-10.0 mu/mL) lower than that of tetracycline. (C) 2011 Elsevier Ltd. All rights reserved.
T2  - Polyhedron
T1  - Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives
VL  - 31
IS  - 1
SP  - 789
EP  - 795
DO  - 10.1016/j.poly.2011.11.006
ER  - 

@article{
author = "Pejović, Anka and Damljanović, Ivan S. and Stevanović, Dragana D. and Vukićević, Mirjana and Novaković, Slađana B. and Bogdanović, Goran A. and Radulovic, Niko and Vukićević, Rastko D.",
year = "2012",
abstract = "Syntheses of three new ferrocene containing heterocycles - 2-ferroceny1-2,3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives - starting from 2-aminoacetophenones and ferrocenecarboxaldehyde was achieved in two steps. The aldol condensation of these substrates gave the corresponding 2-aminochalcones in the first stage, whereas a further intramolecular cyclization gives the final products. This cyclization was performed by either a solvent-free microwave irradiation (500 W/5 min) of a mixture of chalcones and mortmorillonite K-10 or by using an acidic catalyst (the mixture of acetic and orthophosphoric acid). The latter method, which can be performed by simple stirring at room temperature or by irradiation in an ultrasonic bath, gave much better results. The obtained compounds were spectrally and electrochemically (cyclic voltammetry) fully characterized, as well as by single-crystal X-ray analysis. A microdilution assay revealed that the three dihydroquinolinones can be regarded as potential lead compounds in the discovery of new antimicrobial drugs due to their very strong and unselective activity towards pathogenic bacteria and one yeast with MIC values (0.01-10.0 mu/mL) lower than that of tetracycline. (C) 2011 Elsevier Ltd. All rights reserved.",
journal = "Polyhedron",
title = "Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives",
volume = "31",
number = "1",
pages = "789-795",
doi = "10.1016/j.poly.2011.11.006"
}

Pejović, A., Damljanović, I. S., Stevanović, D. D., Vukićević, M., Novaković, S. B., Bogdanović, G. A., Radulovic, N.,& Vukićević, R. D.. (2012). Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives. in Polyhedron, 31(1), 789-795.
https://doi.org/10.1016/j.poly.2011.11.006

Pejović A, Damljanović IS, Stevanović DD, Vukićević M, Novaković SB, Bogdanović GA, Radulovic N, Vukićević RD. Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives. in Polyhedron. 2012;31(1):789-795.
doi:10.1016/j.poly.2011.11.006 .

Pejović, Anka, Damljanović, Ivan S., Stevanović, Dragana D., Vukićević, Mirjana, Novaković, Slađana B., Bogdanović, Goran A., Radulovic, Niko, Vukićević, Rastko D., "Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives" in Polyhedron, 31, no. 1 (2012):789-795,
https://doi.org/10.1016/j.poly.2011.11.006 . .

TY  - JOUR
AU  - Stevanović, Dragana D.
AU  - Pejović, Anka
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Divjakovic, Vladimir
AU  - Vukićević, Rastko D.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4674
AB  - Recrystallization of the title compound, [Fe(C5H5)(C14H13N2O3)], from a mixture of n-hexane and dichloromethane gave the new polymorph, denoted (I), which crystallizes in the same space group (P (1) over bar) as the previously reported structure, denoted (II). The Fe-C distances in (I) range from 2.015 (3) to 2.048 (2) angstrom and the average value of the C-C bond lengths in the two cyclopentadienyl (Cp) rings is 1.403 (13) angstrom. As indicated by the smallest C-Cg1-Cg2-C torsion angle of 1.4 degrees (Cg1 and Cg2 are the centroids of the two Cp rings), the orientation of the Cp rings in (I) is more eclipsed than in the case of (II), for which the value was 15.3 degrees. Despite the pronounced conformational similarity between (I) and (II), the formation of self-complementary N-H center dot center dot center dot O hydrogen-bonded dimers represents the only structural motif common to the two polymorphs. In the extended structure, molecules of (I) utilize C-H center dot center dot center dot O hydrogen bonds and, unlike (II), an extensive set of intermolecular C-H center dot center dot center dot pi interactions. Finger-print plots based on Hirshfeld surfaces are used to compare the packing of the two polymorphs.
T2  - Acta Crystallographica. Section C: Crystal Structure Communications
T1  - A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one
VL  - 68
SP  - M37
EP  - M40
DO  - 10.1107/S0108270112000765
ER  - 

@article{
author = "Stevanović, Dragana D. and Pejović, Anka and Novaković, Slađana B. and Bogdanović, Goran A. and Divjakovic, Vladimir and Vukićević, Rastko D.",
year = "2012",
abstract = "Recrystallization of the title compound, [Fe(C5H5)(C14H13N2O3)], from a mixture of n-hexane and dichloromethane gave the new polymorph, denoted (I), which crystallizes in the same space group (P (1) over bar) as the previously reported structure, denoted (II). The Fe-C distances in (I) range from 2.015 (3) to 2.048 (2) angstrom and the average value of the C-C bond lengths in the two cyclopentadienyl (Cp) rings is 1.403 (13) angstrom. As indicated by the smallest C-Cg1-Cg2-C torsion angle of 1.4 degrees (Cg1 and Cg2 are the centroids of the two Cp rings), the orientation of the Cp rings in (I) is more eclipsed than in the case of (II), for which the value was 15.3 degrees. Despite the pronounced conformational similarity between (I) and (II), the formation of self-complementary N-H center dot center dot center dot O hydrogen-bonded dimers represents the only structural motif common to the two polymorphs. In the extended structure, molecules of (I) utilize C-H center dot center dot center dot O hydrogen bonds and, unlike (II), an extensive set of intermolecular C-H center dot center dot center dot pi interactions. Finger-print plots based on Hirshfeld surfaces are used to compare the packing of the two polymorphs.",
journal = "Acta Crystallographica. Section C: Crystal Structure Communications",
title = "A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one",
volume = "68",
pages = "M37-M40",
doi = "10.1107/S0108270112000765"
}

Stevanović, D. D., Pejović, A., Novaković, S. B., Bogdanović, G. A., Divjakovic, V.,& Vukićević, R. D.. (2012). A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one. in Acta Crystallographica. Section C: Crystal Structure Communications, 68, M37-M40.
https://doi.org/10.1107/S0108270112000765

Stevanović DD, Pejović A, Novaković SB, Bogdanović GA, Divjakovic V, Vukićević RD. A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one. in Acta Crystallographica. Section C: Crystal Structure Communications. 2012;68:M37-M40.
doi:10.1107/S0108270112000765 .

Stevanović, Dragana D., Pejović, Anka, Novaković, Slađana B., Bogdanović, Goran A., Divjakovic, Vladimir, Vukićević, Rastko D., "A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one" in Acta Crystallographica. Section C: Crystal Structure Communications, 68 (2012):M37-M40,
https://doi.org/10.1107/S0108270112000765 . .

TY  - JOUR
AU  - Leka, Zorica
AU  - Novaković, Slađana B.
AU  - Pejović, Anka
AU  - Bogdanović, Goran A.
AU  - Vukićević, Rastko D.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4724
AB  - The title ferrocene derivative, [Fe(C5H5)(C14H13FNO)], crystallizes in the same space group with similar unit-cell parameters as the derivatives 3-anilino-1-ferrocenylpropan-1- one [Leka et al. (2012). Acta Cryst. E68, m229] and 1-ferrocenyl- 3-(4-methylanilino) propan-1-one [Leka et al. (2012). Acta Cryst. E68, m230]. The dihedral angle between the best planes of the benzene ring and the substituted cyclopentadienyl ring is 83.4 (1)degrees. The presence of the electronegative fluoro substituent in the meta position of the aniline group does not alter the crystal packing compared to the other two derivatives. The molecules are connected into centrosymmetric dimers via N-H center dot center dot center dot O hydrogen bonds. In addition, C-H center dot center dot center dot O and C-H center dot center dot center dot N contacts stabilize the crystal packing.
T2  - Acta Crystallographica. Section E: Structure Reports Online
T1  - 1-Ferrocenyl-3-(3-fluoroanilino)propan-1-one
VL  - 68
SP  - M231
EP  - U1368
DO  - 10.1107/S1600536812003510
ER  - 

@article{
author = "Leka, Zorica and Novaković, Slađana B. and Pejović, Anka and Bogdanović, Goran A. and Vukićević, Rastko D.",
year = "2012",
abstract = "The title ferrocene derivative, [Fe(C5H5)(C14H13FNO)], crystallizes in the same space group with similar unit-cell parameters as the derivatives 3-anilino-1-ferrocenylpropan-1- one [Leka et al. (2012). Acta Cryst. E68, m229] and 1-ferrocenyl- 3-(4-methylanilino) propan-1-one [Leka et al. (2012). Acta Cryst. E68, m230]. The dihedral angle between the best planes of the benzene ring and the substituted cyclopentadienyl ring is 83.4 (1)degrees. The presence of the electronegative fluoro substituent in the meta position of the aniline group does not alter the crystal packing compared to the other two derivatives. The molecules are connected into centrosymmetric dimers via N-H center dot center dot center dot O hydrogen bonds. In addition, C-H center dot center dot center dot O and C-H center dot center dot center dot N contacts stabilize the crystal packing.",
journal = "Acta Crystallographica. Section E: Structure Reports Online",
title = "1-Ferrocenyl-3-(3-fluoroanilino)propan-1-one",
volume = "68",
pages = "M231-U1368",
doi = "10.1107/S1600536812003510"
}

Leka, Z., Novaković, S. B., Pejović, A., Bogdanović, G. A.,& Vukićević, R. D.. (2012). 1-Ferrocenyl-3-(3-fluoroanilino)propan-1-one. in Acta Crystallographica. Section E: Structure Reports Online, 68, M231-U1368.
https://doi.org/10.1107/S1600536812003510

Leka Z, Novaković SB, Pejović A, Bogdanović GA, Vukićević RD. 1-Ferrocenyl-3-(3-fluoroanilino)propan-1-one. in Acta Crystallographica. Section E: Structure Reports Online. 2012;68:M231-U1368.
doi:10.1107/S1600536812003510 .

Leka, Zorica, Novaković, Slađana B., Pejović, Anka, Bogdanović, Goran A., Vukićević, Rastko D., "1-Ferrocenyl-3-(3-fluoroanilino)propan-1-one" in Acta Crystallographica. Section E: Structure Reports Online, 68 (2012):M231-U1368,
https://doi.org/10.1107/S1600536812003510 . .

TY  - JOUR
AU  - Damljanović, Ivan S.
AU  - Stevanović, Dragana D.
AU  - Pejović, Anka
AU  - Vukićević, Mirjana
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Mihajlov-Krstev, Tatjana
AU  - Radulovic, Niko
AU  - Vukićević, Rastko D.
PY  - 2011
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4552
AB  - Syntheses of fourteen new 3-(arylamino)-1-ferrocenylpropan-1-ones have been achieved in good to excellent yields by an aza-Michael addition of different arylamines to acryloylferrocene. The reaction was performed by microwave (MW) irradiation (500 W/5 min) of a mixture of reactants and montmorillonite K-10, without a solvent. The obtained compounds were spectrally and electrochemically (cyclic voltammetry) fully characterized, whereas single-crystal X-ray analysis has been performed for three of them. In a microdilution assay, all of the compounds were shown to have a broad-spectrum effect on Gram-negative and -positive bacteria, although the degree of inhibition varied. A notable activity was observed for all compounds in inhibiting the growth of an important human pathogen Staphylococcus aureus. (C) 2011 Elsevier B.V. All rights reserved.
T2  - Journal of Organometallic Chemistry
T1  - Antibacterial 3-(arylamino)-1-ferrocenylpropan-1-ones: Synthesis, spectral, electrochemical and structural characterization
VL  - 696
IS  - 23
SP  - 3703
EP  - 3713
DO  - 10.1016/j.jorganchem.2011.08.016
ER  - 

@article{
author = "Damljanović, Ivan S. and Stevanović, Dragana D. and Pejović, Anka and Vukićević, Mirjana and Novaković, Slađana B. and Bogdanović, Goran A. and Mihajlov-Krstev, Tatjana and Radulovic, Niko and Vukićević, Rastko D.",
year = "2011",
abstract = "Syntheses of fourteen new 3-(arylamino)-1-ferrocenylpropan-1-ones have been achieved in good to excellent yields by an aza-Michael addition of different arylamines to acryloylferrocene. The reaction was performed by microwave (MW) irradiation (500 W/5 min) of a mixture of reactants and montmorillonite K-10, without a solvent. The obtained compounds were spectrally and electrochemically (cyclic voltammetry) fully characterized, whereas single-crystal X-ray analysis has been performed for three of them. In a microdilution assay, all of the compounds were shown to have a broad-spectrum effect on Gram-negative and -positive bacteria, although the degree of inhibition varied. A notable activity was observed for all compounds in inhibiting the growth of an important human pathogen Staphylococcus aureus. (C) 2011 Elsevier B.V. All rights reserved.",
journal = "Journal of Organometallic Chemistry",
title = "Antibacterial 3-(arylamino)-1-ferrocenylpropan-1-ones: Synthesis, spectral, electrochemical and structural characterization",
volume = "696",
number = "23",
pages = "3703-3713",
doi = "10.1016/j.jorganchem.2011.08.016"
}

Damljanović, I. S., Stevanović, D. D., Pejović, A., Vukićević, M., Novaković, S. B., Bogdanović, G. A., Mihajlov-Krstev, T., Radulovic, N.,& Vukićević, R. D.. (2011). Antibacterial 3-(arylamino)-1-ferrocenylpropan-1-ones: Synthesis, spectral, electrochemical and structural characterization. in Journal of Organometallic Chemistry, 696(23), 3703-3713.
https://doi.org/10.1016/j.jorganchem.2011.08.016

Damljanović IS, Stevanović DD, Pejović A, Vukićević M, Novaković SB, Bogdanović GA, Mihajlov-Krstev T, Radulovic N, Vukićević RD. Antibacterial 3-(arylamino)-1-ferrocenylpropan-1-ones: Synthesis, spectral, electrochemical and structural characterization. in Journal of Organometallic Chemistry. 2011;696(23):3703-3713.
doi:10.1016/j.jorganchem.2011.08.016 .

Damljanović, Ivan S., Stevanović, Dragana D., Pejović, Anka, Vukićević, Mirjana, Novaković, Slađana B., Bogdanović, Goran A., Mihajlov-Krstev, Tatjana, Radulovic, Niko, Vukićević, Rastko D., "Antibacterial 3-(arylamino)-1-ferrocenylpropan-1-ones: Synthesis, spectral, electrochemical and structural characterization" in Journal of Organometallic Chemistry, 696, no. 23 (2011):3703-3713,
https://doi.org/10.1016/j.jorganchem.2011.08.016 . .