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Direct N-acetyl enamine formation: lithium bromide mediated addition of methyllithium to nitriles.
Savarin, Cécile G; Boice, Geneviève N; Murry, Jerry A; Corley, Edward; DiMichele, Lisa; Hughes, Dave.
Afiliação
  • Savarin CG; Department of Process Research, Merck Research Laboratories, Merck & Company, P.O. Box 2000, Rahway, NJ 07065, USA. cecile_savarin@merck.com
Org Lett ; 8(18): 3903-6, 2006 Aug 31.
Article em En | MEDLINE | ID: mdl-16928034
ABSTRACT
An improved protocol for N-acetyl enamine formation is disclosed which involves LiBr-mediated addition of MeLi to substituted nitriles. The resulting enamides are isolated in high yields and excellent purity which permits subsequent hydrogenation at very low catalyst loading.
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2006 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Idioma: En Ano de publicação: 2006 Tipo de documento: Article