Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/95736
Type: Artigo de periódico
Title: Intramolecular Interception Of Reactive Intermediates In The Raney Nickel 'generated In Situ' Reduction Of Oximes. Synthetic And Mechanistic Implications
Author: Kascheres A.
Rodrigues R.A.F.
Abstract: Reduction of oximes 4, obtained from 1,5 di-hydro-2H-pyrrol-2-ones 3, with Raney nickel 'generated in situ' afforded pyrrolo [3,2b] pyrrolone derivatives 6 and 7 and, in some cases, amines 5. The reduction of 4 with W7 Raney nickel afforded only amines 5. Mechanistic aspects of these reductions were investigated. The formation of 6 and 7 is attributed to the deactivation of the catalyst by sodium hydroxide.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/0040-4020(96)00768-5
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0030607170&partnerID=40&md5=3830a739f27ab546a4817228175167a4
Date Issue: 1996
Appears in Collections:Unicamp - Artigos e Outros Documentos

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