Secondary Mannich Bases Via Trimethylsilyl Trifluoromethanesulphonate Promoted Addition Of Silyl Enol Ethers To Schiff Bases

dc.creatorPilli R.A.
dc.creatorRussowsky D.
dc.date1987
dc.date2015-06-30T13:40:39Z
dc.date2015-11-26T14:37:03Z
dc.date2015-06-30T13:40:39Z
dc.date2015-11-26T14:37:03Z
dc.date.accessioned2018-03-28T21:41:15Z
dc.date.available2018-03-28T21:41:15Z
dc.identifier
dc.identifierJournal Of The Chemical Society, Chemical Communications. , v. , n. 14, p. 1053 - 1054, 1987.
dc.identifier224936
dc.identifier10.1039/C39870001053
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-37049067428&partnerID=40&md5=729275395abf3fae1c9ccc390af5e466
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/98172
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/98172
dc.identifier2-s2.0-37049067428
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1248995
dc.descriptionA convenient route to N-aryl-β-aminoketones is reported involving addition of silyl enol ethers to Schiff bases activated with 15 mol % of trimethylsilyl trifluoromethanesulphonate.
dc.description
dc.description14
dc.description1053
dc.description1054
dc.languageen
dc.publisher
dc.relationJournal of the Chemical Society, Chemical Communications
dc.rightsaberto
dc.sourceScopus
dc.titleSecondary Mannich Bases Via Trimethylsilyl Trifluoromethanesulphonate Promoted Addition Of Silyl Enol Ethers To Schiff Bases
dc.typeArtículos de revistas


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