dc.creator | Maslak, Veselin | |
dc.creator | Matović, Radomir | |
dc.creator | Saičić, Radomir N. | |
dc.date.accessioned | 2019-04-29T07:27:53Z | |
dc.date.available | 2019-04-29T07:27:53Z | |
dc.date.issued | 2004 | |
dc.identifier.issn | 0040-4020 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/2768 | |
dc.description.abstract | Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic work-up, affords butanolides in moderate/good yields. With epihalohydrins the reaction is regioselective and occurs at the less substituted end of the epoxide; the gamma-haloalkyl-gamma-butanolides thus obtained can be further transformed into various products. (C) 2004 Elsevier Ltd. All rights reserved. | en |
dc.publisher | Oxford : Pergamon-Elsevier Science Ltd | |
dc.rights | restrictedAccess | |
dc.source | Tetrahedron | |
dc.subject | epoxides | en |
dc.subject | ketene acetals | en |
dc.subject | lactones | en |
dc.subject | titanium and compounds | en |
dc.subject | alkylation | en |
dc.title | Reaction of silyl ketene acetals with epoxides: a new method for the synthesis of gamma-butanolides | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Матовић, Радомир; Саичић, Радомир Н.; Маслак, Веселин; | |
dc.citation.volume | 60 | |
dc.citation.issue | 40 | |
dc.citation.spage | 8957 | |
dc.citation.epage | 8966 | |
dc.citation.other | 60(40): 8957-8966 | |
dc.citation.rank | M21 | |
dc.identifier.doi | 10.1016/j.tet.2004.07.007 | |
dc.identifier.scopus | 2-s2.0-4444296427 | |
dc.identifier.wos | 000223935100021 | |
dc.type.version | publishedVersion | en |