Bifunctional guanidine via an amino amide skeleton for asymmetric michael reactions of ß-ketoesters with nitroolefins: A concise synthesis of bicyclic β- Amino acids

Angewandte Chemie - International Edition

Volumn 48, Issue 28, 2009, Pages 5195-5198

  Yu, Zhipeng ^a   Liu, Xiaohua ^a   Zhou, Lin ^a   Lin, Lili ^a   Feng, Xiaoming ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

Amino acids; Asymmetric synthesis; Guanidines; Michael addition; Organocatalysis

Indexed keywords

AMINO ACID ESTERS; ASYMMETRIC SYNTHESIS; BIFUNCTIONAL; CONCISE SYNTHESIS; DUAL ACTIVATION; EFFICIENT SYNTHESIS; GUANIDINES; KETO ESTER; MICHAEL ADDITION; MICHAEL ADDITIONS; MICHAEL REACTIONS; NITROOLEFINS; ORGANOCATALYSIS;

ADDITION REACTIONS; AMIDES; AMINATION; AMINO ACIDS; CATALYSIS; CHEMICAL ACTIVATION; ELECTRON TRANSITIONS; ESTERS; ORGANIC ACIDS; RATE CONSTANTS; REACTION KINETICS; SELF ASSEMBLY;

AMINES;

ALKENE; AMIDE; AMINO ACID; BICYCLO COMPOUND; ESTER; GUANIDINE;

CATALYSIS; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALKENES; AMIDES; AMINO ACIDS, CYCLIC; BICYCLO COMPOUNDS; CATALYSIS; ESTERS; GUANIDINE; STEREOISOMERISM;

EID: 70349782136     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200901337     Document Type: Article

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