Highly regio-, diastereo-, and enantioselective 1,6- and 1,8-additions of azlactones to Di- and trienyl N -acylpyrroles

Journal of the American Chemical Society

Volumn 134, Issue 47, 2012, Pages 19370-19373

  Uraguchi, Daisuke ^a   Yoshioka, Ken ^a   Ueki, Yusuke ^a   Ooi, Takashi ^a  

^a NAGOYA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AZLACTONES; ENANTIOSELECTIVE; MICHAEL ADDITIONS; STEREOCONTROL;

ADDITION REACTIONS;

ENANTIOSELECTIVITY;

AZLACTONE DERIVATIVE; DIENYL N ACYLPYRROLE DERIVATIVE; LACTONE DERIVATIVE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; DIASTEREOSELECTIVITY; ENANTIOSELECTIVITY; MICHAEL ADDITION; REGIOSELECTIVITY; SUBSTITUTION REACTION; TEMPERATURE;

LACTONES; MOLECULAR STRUCTURE; PYRROLES; STEREOISOMERISM;

EID: 84870359712     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja310209g     Document Type: Article

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