Free radical mediated construction of small ring compounds: The double annulation of bicyclo[3.1.0]hex-2-enes

dc.creator	Ferjančić, Zorana
dc.creator	Saičić, Radomir
dc.creator	Čeković, Živorad
dc.date.accessioned	2018-11-22T00:01:46Z
dc.date.available	2018-11-22T00:01:46Z
dc.date.issued	1997
dc.identifier.issn	0040-4039
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/2591
dc.description.abstract	A free radical approach to fused cyclopropane derivatives is described. Homolytic decomposition of thiohydroxamic esters 4a-e in the presence of dimethyl acetylendicarboxylate affords bicyclo[3.1.0]hex-2-enes 6a-e in moderate yields. (C) 1997 Elsevier Science Ltd.	en
dc.publisher	Pergamon-Elsevier Science Ltd, Oxford
dc.rights	restrictedAccess
dc.source	Tetrahedron Letters
dc.title	Free radical mediated construction of small ring compounds: The double annulation of bicyclo[3.1.0]hex-2-enes	en
dc.type	article
dc.rights.license	ARR
dcterms.abstract	Ферјанчић, Зорана; Саичић, Радомир; Цековиц, З;
dc.citation.volume	38
dc.citation.issue	23
dc.citation.spage	4165
dc.citation.epage	4168
dc.identifier.wos	A1997XD51100047
dc.identifier.doi	10.1016/S0040-4039(97)00811-3
dc.citation.other	38(23): 4165-4168
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-0342617556