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Organocatalytic, Organic Oxidant Promoted, Enamine C−H Oxidation/Cyclopropanation Reaction
dc.creator | Džambaski, Zdravko | |
dc.creator | Bondžić, Aleksandra M. | |
dc.creator | Triandafillidi, Ierasia | |
dc.creator | Kokotos, Christoforos G. | |
dc.creator | Bondžić, Bojan P. | |
dc.date.accessioned | 2021-11-01T07:16:42Z | |
dc.date.accessioned | 2021-11-08T13:30:09Z | |
dc.date.available | 2021-11-01T07:16:42Z | |
dc.date.available | 2021-11-08T13:30:09Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 1615-4150 | |
dc.identifier.uri | https://vinar.vin.bg.ac.rs/handle/123456789/9871 | |
dc.description.abstract | Herein, we demonstrate that organic, single-electron oxidant in the presence of diarylprolinol silylether type catalyst serves as a tool for the transformation of electron-rich enamines to iminium ions. These iminium ions take part in a subsequent Michael-initiated ring-closure (MIRC) reaction with in situ present nucleophile giving rise to overall cyclopropanation reaction of saturated aldehydes. Stereodefined cyclopropanes are obtained in high yields and selectivities. This one-pot transformation represents the additional example of saturated aldehydes being used in the coupled one-pot processes. (Figure presented.). | en |
dc.language.iso | en | en |
dc.relation | info:eu-repo/grantAgreement/MESTD/inst-2020/200026/RS// | |
dc.relation | The State Scholarships Foundation (IKY) [MIS 5033021] | |
dc.relation | HFRI [655] | |
dc.rights | restrictedAccess | |
dc.source | Advanced Synthesis and Catalysis | |
dc.subject | Cyclopropanation | en |
dc.subject | C−H oxidation | en |
dc.subject | Diarylprolinols | en |
dc.subject | One-pot reaction. | en |
dc.subject | Organocatalysis | en |
dc.title | Organocatalytic, Organic Oxidant Promoted, Enamine C−H Oxidation/Cyclopropanation Reaction | en |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.volume | 363 | |
dc.citation.issue | 16 | |
dc.citation.spage | 4002 | |
dc.citation.epage | 4008 | |
dc.identifier.wos | 000667158900001 | |
dc.identifier.doi | 10.1002/adsc.202100630 | |
dc.citation.rank | aM21 | |
dc.type.version | publishedVersion | sr |
dc.identifier.scopus | 2-s2.0-8510894343 |
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