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dc.creatorDžambaski, Zdravko
dc.creatorBondžić, Aleksandra M.
dc.creatorTriandafillidi, Ierasia
dc.creatorKokotos, Christoforos G.
dc.creatorBondžić, Bojan
dc.date.accessioned2021-11-01T07:16:42Z
dc.date.available2021-11-01T07:16:42Z
dc.date.issued2021
dc.identifier.issn1615-4150
dc.identifier.issn1615-4169
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4823
dc.description.abstractHerein, 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.).sr
dc.language.isoensr
dc.publisherWileysr
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200026/RS//sr
dc.relationThe State Scholarships Foundation (IKY) , MIS 5033021sr
dc.rightsrestrictedAccesssr
dc.sourceAdvanced Synthesis and Catalysissr
dc.subjectCyclopropanationsr
dc.subjectC−H oxidationsr
dc.subjectDiarylprolinolssr
dc.subjectOne-pot reaction.sr
dc.subjectOrganocatalysissr
dc.titleOrganocatalytic, Organic Oxidant Promoted, Enamine C−H Oxidation/Cyclopropanation Reactionsr
dc.typearticlesr
dc.rights.licenseARRsr
dc.citation.volume363
dc.citation.issue16
dc.citation.spage4002
dc.citation.epage4008
dc.citation.rankaM21~
dc.identifier.doi10.1002/adsc.202100630
dc.identifier.scopus2-s2.0-85108943435
dc.identifier.wos000667158900001
dc.type.versionpublishedVersionsr


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