Conjugate reduction of alpha,beta-unsaturated carbonyl compounds. Selective inhibition of benzyl ether hydrogenolysis by NH4OH/MeOH

dc.creatorDias, LC
dc.creatorCampano, PL
dc.date1998
dc.dateJAN-FEB
dc.date2014-12-02T16:30:10Z
dc.date2015-11-26T17:39:03Z
dc.date2014-12-02T16:30:10Z
dc.date2015-11-26T17:39:03Z
dc.date.accessioned2018-03-29T00:20:41Z
dc.date.available2018-03-29T00:20:41Z
dc.identifierJournal Of The Brazilian Chemical Society. Soc Brasileira Quimica, v. 9, n. 1, n. 97, n. 99, 1998.
dc.identifier0103-5053
dc.identifierWOS:000074749200017
dc.identifier10.1590/S0103-50531998000100017
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/56553
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/56553
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/56553
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1286362
dc.descriptionA series of alpha,beta-unsaturated alkyl and aryl ketones, esters and N-methoxy-N-methyl-amides (Weinreb amides) containing an O-benzyl protecting group undergo conjugate reduction by H-2/Pd/C in the presence of 2N NH4OH/MeOH at room temperature and ordinary pressure leaving the benzyl group intact.
dc.description9
dc.description1
dc.description97
dc.description99
dc.languageen
dc.publisherSoc Brasileira Quimica
dc.publisherSao Paulo
dc.publisherBrasil
dc.relationJournal Of The Brazilian Chemical Society
dc.relationJ. Braz. Chem. Soc.
dc.rightsaberto
dc.sourceWeb of Science
dc.subjectconjugate reduction
dc.subjectinhibition of benzyl ether hydrogenolysis
dc.subjectchemoselective reduction of alpha,beta-unsaturated compounds
dc.subjectselective catalytic hydrogenation
dc.titleConjugate reduction of alpha,beta-unsaturated carbonyl compounds. Selective inhibition of benzyl ether hydrogenolysis by NH4OH/MeOH
dc.typeArtículos de revistas


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