Synthesis of acylsilanes via oxidative hydrolysis of 2-silyl-1,3-dithianes mediated by N-bromosuccinimide

dc.creatorPatrocinio, AF
dc.creatorMoran, PJS
dc.date2000
dc.dateMAY 29
dc.date2014-12-02T16:24:26Z
dc.date2015-11-26T16:30:37Z
dc.date2014-12-02T16:24:26Z
dc.date2015-11-26T16:30:37Z
dc.date.accessioned2018-03-28T23:11:40Z
dc.date.available2018-03-28T23:11:40Z
dc.identifierJournal Of Organometallic Chemistry. Elsevier Science Sa, v. 603, n. 2, n. 220, n. 224, 2000.
dc.identifier0022-328X
dc.identifierWOS:000088285800012
dc.identifier10.1016/S0022-328X(00)00181-9
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74113
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/74113
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/74113
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1270007
dc.descriptionThe oxidative method for the hydrolysis of 1,3-dithianes was applied to 2-silyl-1,3-dithianes using N-bromosuccinimide providing acylsilanes with good yields under a short reaction period. The oxidation of aroylsilanes to carboxylic acid was prevented by the addition of bases and the lowering of the reaction temperature. (C) 2000 Elsevier Science S.A. All rights reserved.
dc.description603
dc.description2
dc.description220
dc.description224
dc.languageen
dc.publisherElsevier Science Sa
dc.publisherLausanne
dc.publisherSuíça
dc.relationJournal Of Organometallic Chemistry
dc.relationJ. Organomet. Chem.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectaroylsilanes
dc.subjectoxidation
dc.subject1,3-dithianes
dc.subjectN-bromosuccinimide
dc.subjectAcyl Silanes
dc.subjectVersatile
dc.titleSynthesis of acylsilanes via oxidative hydrolysis of 2-silyl-1,3-dithianes mediated by N-bromosuccinimide
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución