Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/79939
Type: Artigo de periódico
Title: Efficient and expeditious protocols for the synthesis of racemic and enantiomerically pure endocyclic enecarbamates from N-acyl lactams and N-acyl pyrrolidines
Author: Oliveira, DF
Miranda, PCML
Correia, CRD
Abstract: A mild, practical, and straightforward protocol for the construction of endocyclic enecarbamates starting from N-acyl lactams and N-acyl pyrrolidines is presented. Lactams were reduced to the corresponding alpha-hydroxycarbamates in good to excellent yields using DIBAL-H, SuperHydride, or NaBH4 followed by beta-elimination (dehydration) promoted by trifluoroacetic anhydride in the presence of hindered nitrogenated bases such as 2,6-lutidine, diisopropylethylamine, or triethylamine. Small variations of this protocol permitted the preparation of several endocyclic enecarbamates (12 examples) in good to excellent overall yields (56-96%). The protocol was demonstrated to be applicable to several ring sizes,compatible with different protecting groups, and to be mild enough to prevent racemization of racemization-prone stereocenters. The efficacy of the procedure in the preparation of enantiomerically pure endocyclic enecarbamates was also demonstrated and compared to the commonly used Shone's protocol, which in our hands led to partial racemization of the endocyclic enecarbamate 18c.
Country: EUA
Editor: Amer Chemical Soc
Rights: fechado
Identifier DOI: 10.1021/jo9903297
Date Issue: 1999
Appears in Collections:Unicamp - Artigos e Outros Documentos

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