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dc.creatorDžambaski, Zdravko
dc.creatorBondžić, Bojan
dc.date.accessioned2019-09-09T09:16:29Z
dc.date.available2019-09-09T09:16:29Z
dc.date.issued2019
dc.identifier.issn1477-0520
dc.identifier.issn1477-0539
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/3063
dc.description.abstractThe organocatalyzed Mannich reaction of unsubstituted and N-aryl-substituted tetrahydroisoquinolines (THIQs) and the Strecker reaction of several N-aryl-substituted THIQs through dehydrogenative C(sp3)–H bond functionalization (cross-dehydrogenative coupling) promoted by organic single electron oxidants DDQ and IBX are presented. The C–H oxidation/Mannich reaction of less reactive N-aryl substituted pyrrolidines is achieved via metal catalyzed photoredox catalysis. Operationally simple procedures provide desired products in an effective and time preserving manner.en
dc.publisherRoyal Society of Chemistry (RSC)en
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172020/RS//
dc.relationCOST action CA15106: C–H Activation in Organic Synthesis (CHAOS)
dc.rightsrestrictedAccess
dc.sourceOrganic & Biomolecular Chemistryen
dc.subjectCross-dehydrogenative coupling
dc.subjectMannich reaction
dc.titleDehydrogenative C(sp3)–H bond functionalization of tetrahydroisoquinolines mediated by organic oxidants under mild conditionsen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractДжамбаски, Здравко; Бонджић, Бојан П.;
dc.rights.holderRoyal Society of Chemistry
dc.citation.volume17
dc.citation.issue26
dc.citation.spage6420
dc.citation.epage6425
dc.citation.rankM21~
dc.identifier.pmid31225575
dc.identifier.doi10.1039/C9OB01090D
dc.identifier.scopus2-s2.0-85068414427
dc.identifier.wos000474089200014
dc.type.versionpublishedVersion


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