Stereoselective Nucleophilic Addition of Potassium Alkyltrifluoroborates to Cyclic N-Acyliminium Ions: a Simple and Mild Approach to Chiral 5-Alkyl-pyrrolidin-2-ones
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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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 |
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 |