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Palladium-Catalyzed Asymmetric Allylic Alkylation of 4-Substituted Isoxazolidin-5-ones: Straightforward Access to ß2,2 -Amino Acids.
Nascimento de Oliveira, Marllon; Arseniyadis, Stellios; Cossy, Janine.
Afiliação
  • Nascimento de Oliveira M; Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI)-ESPCI, Paris/CNRS (UMR8231)/PSL* Research University, 10 rue Vauquelin, 75231, Paris Cedex 05, France.
  • Arseniyadis S; Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI)-ESPCI, Paris/CNRS (UMR8231)/PSL* Research University, 10 rue Vauquelin, 75231, Paris Cedex 05, France.
  • Cossy J; Queen Mary, University of London, School of Biological and Chemical Sciences, Mile End Road, London, E1 4NS, UK.
Chemistry ; 24(19): 4810-4814, 2018 Apr 03.
Article em En | MEDLINE | ID: mdl-29436035
ABSTRACT
We report here an unprecedented and highly enantioselective palladium-catalyzed allylic alkylation applied to 4-substituted isoxazolidin-5-ones. Ultimately, the process provides a straightforward access to ß2,2 -amino acids bearing an all-carbon quaternary stereogenic center in great yields and a high degree of enantioselectivity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio / Aminoácidos / Isoxazóis Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio / Aminoácidos / Isoxazóis Idioma: En Ano de publicação: 2018 Tipo de documento: Article