Rapid [3,3] sigmatropic rearrangements of allylic thiono chloroformates

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dc.authoridZaim, Omer/0000-0002-3472-5611
dc.authorwosidZaim, Ömer/AAI-1470-2021
dc.authorwosidZaim, Omer/Q-7770-2019
dc.contributor.authorZaim, Ö
dc.date.accessioned2024-06-12T11:13:24Z
dc.date.available2024-06-12T11:13:24Z
dc.date.issued1999
dc.departmentTrakya Üniversitesien_US
dc.description.abstractTreatment of allylic alcohols with thiophosgene and pyridine gives thiolo chloroformates directly at room temperature, presumably via very rapid [3,3] sigmatropic rearrangements of thiono chloroformates. Synthesis of allyl thiono chloroformate from allyl alcohol, sodium hydride and thiophosgene at low temperature and warming up to room temperature supports this finding. (C) 1999 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/S0040-4039(99)01693-7
dc.identifier.endpage8062en_US
dc.identifier.issn0040-4039
dc.identifier.issue46en_US
dc.identifier.scopus2-s2.0-0033550255en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage8059en_US
dc.identifier.urihttps://doi.org/10.1016/S0040-4039(99)01693-7
dc.identifier.urihttps://hdl.handle.net/20.500.14551/23544
dc.identifier.volume40en_US
dc.identifier.wosWOS:000083342700006en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedron Lettersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRearrangementsen_US
dc.subjectAlcoholsen_US
dc.subjectThiocarbonylen_US
dc.subjectThiocarbamateen_US
dc.subjectDithiocarbonatesen_US
dc.subjectAlcoholsen_US
dc.subjectAcidsen_US
dc.titleRapid [3,3] sigmatropic rearrangements of allylic thiono chloroformatesen_US
dc.typeArticleen_US

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