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dc.creatorSaičić, Radomir
dc.creatorČeković, Z.
dc.date.accessioned2018-11-22T00:00:20Z
dc.date.available2018-11-22T00:00:20Z
dc.date.issued1990
dc.identifier.issn0040-4039
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/21
dc.description.abstractBy thermally or photolytically induced decomposition of O-acyl derivatives of N-hydroxypyridine-2-thione or other thiohydroxamic esters, in the presence of an excess of electron deficient olefins, 2-vinylcyclopentane derivatives were obtained. This sequence of addition/cyclization/elimination reaction is mediated by a phenylthio radical. © 1990.en
dc.rightsopenAccess
dc.sourceTetrahedron Letters
dc.titleRadical annulation methodology. 2-Vinylcyclopentane derivative formation by a 3 + 2 cycloaddition reactionen
dc.typearticle
dc.rights.licenseARR
dc.citation.volume31
dc.citation.issue29
dc.citation.spage4203
dc.citation.epage4206
dc.identifier.doi10.1016/S0040-4039(00)97582-8
dc.citation.other31(29): 4203-4206
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-0025308645
dc.identifier.rcubKon_1000


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