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Readily tunable and bifunctional L-prolinamide derivatives: design and application in the direct enantioselective Aldol reactions.
Chen, Jia-Rong; Lu, Hai-Hua; Li, Xin-Yong; Cheng, Lin; Wan, Jian; Xiao, Wen-Jing.
Afiliação
  • Chen JR; Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China.
Org Lett ; 7(20): 4543-5, 2005 Sep 29.
Article em En | MEDLINE | ID: mdl-16178579
ABSTRACT
[reaction see text] Readily tunable and bifunctional L-prolinamides as novel organocatalysts have been developed, and their catalytic activities were evaluated in the direct asymmetric Aldol reactions of various aromatic aldehydes and cyclohexanone. High isolated yields (up to 94%), enantioselectivities (up to 99% ee), and anti-diastereoselectivities (up to 991) were obtained under the optimal conditions.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prolina / Desenho de Fármacos / Aldeídos Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2005 Tipo de documento: Article País de afiliação: China
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prolina / Desenho de Fármacos / Aldeídos Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2005 Tipo de documento: Article País de afiliação: China