Rationally designed amide donors for organocatalytic asymmetric michael reactions

Angewandte Chemie - International Edition

Volumn 51, Issue 22, 2012, Pages 5381-5385

  Tan, Bin ^a   Hernández Torres, Gloria ^a,b   Barbas III, Carlos F ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

amides; asymmetric synthesis; cinchona alkaloids; Michael addition; organocatalysis

Indexed keywords

AMIDE DONORS; ASYMMETRIC SYNTHESIS; CINCHONA ALKALOID; LEAVING GROUPS; MICHAEL ADDITIONS; MICHAEL REACTIONS; OPTICAL YIELDS; ORGANOCATALYSIS; ORGANOCATALYTIC;

ADDITION REACTIONS; CATALYSIS; REACTION KINETICS; UREA;

AMIDES;

AMIDE; PYRAZOLE DERIVATIVE; UREA;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; DRUG DESIGN; STEREOISOMERISM;

AMIDES; CATALYSIS; DRUG DESIGN; MOLECULAR STRUCTURE; PYRAZOLES; STEREOISOMERISM; UREA;

EID: 84861514836     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201200996     Document Type: Article

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