Enantioselective Tandem O-Nitroso Aldol/Michael Reaction

Journal of the American Chemical Society

Volumn 126, Issue 19, 2004, Pages 5962-5963

  Yamamoto, Yuhei ^a   Momiyama, Norie ^a   Yamamoto, Hisashi ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL REACTION; ARTICLE; CHEMICAL ANALYSIS; DIELS ALDER REACTION; ENANTIOSELECTIVITY; MICHAEL ADDITION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

AMINES; CATALYSIS; KETONES; NAPHTHALENES; NITROSO COMPOUNDS; SILVER; STEREOISOMERISM;

EID: 2442435852     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja049741g     Document Type: Article

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23. The same reaction catalyzed by L-proline was also examined. Although the reaction provided 98-99% ee, the yields were < 1-40%. The detailed results are described in Supporting Information.
24. The structure by X-ray analysis is shown in Supporting Information.
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