Stereoselective Nucleophilic Addition of Potassium Alkyltrifluoroborates to Cyclic N-Acyliminium Ions: a Simple and Mild Approach to Chiral 5-Alkyl-pyrrolidin-2-ones


Autoria(s): VIEIRA, Adriano S.; FERREIRA, Fernando P.; GUAREZEMINI, Alexandre S.; STEFANI, Helio A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

The stereoselective nucleophilic addition of potassium alkyltrifluoroborates to cyclic N-acyliminium ions derived from N-benzyl-3,4,5-triacetoxy-pyrrolidin-2-one, which affords 5-substituted-pyrrolidin-2-ones, is described. The products are obtained in moderate to good yields and are produced predominantly as the anti diastereomer.

Identificador

AUSTRALIAN JOURNAL OF CHEMISTRY, v.62, n.8, p.909-916, 2009

0004-9425

http://producao.usp.br/handle/BDPI/31240

10.1071/CH09067

http://dx.doi.org/10.1071/CH09067

Idioma(s)

eng

Publicador

CSIRO PUBLISHING

Relação

Australian Journal of Chemistry

Direitos

restrictedAccess

Copyright CSIRO PUBLISHING

Palavras-Chave #ALPHA-METHOXY AMIDES #COMPLEX-CATALYZED ALLYLATION #ELECTROORGANIC CHEMISTRY #ASYMMETRIC-SYNTHESIS #FACILE SYNTHESIS #SUBSTITUTION-REACTIONS #SYNTHETIC APPLICATIONS #CARBON NUCLEOPHILES #(S)-MALIC ACID #BORONIC ACIDS #Chemistry, Multidisciplinary
Tipo

article

proceedings paper

publishedVersion