Highly enantioselective synthesis of 3,4-dihydropyrans through a phosphine-catalyzed [4+2] annulation of allenones and β,γ-unsaturated α-keto esters

Journal of the American Chemical Society

Volumn 137, Issue 1, 2015, Pages 54-57

  Yao, Weijun ^a   Dou, Xiaowei ^a   Lu, Yixin ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CATALYSIS; ENANTIOSELECTIVITY; ESTERIFICATION; ESTERS; KETONES;

BI-FUNCTIONAL; DIHYDROPYRAN; ENANTIOSELECTIVE SYNTHESIS; HIGH YIELD; KETO ESTER; SYNTHONS;

PHOSPHORUS COMPOUNDS;

3,4 DIHYDROPYRAN DERIVATIVE; ALLENONE DERIVATIVE; ALPHA KETO ESTER; ESTER; KETONE; PHOSPHINE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; CYCLOADDITION; ENANTIOSELECTIVITY; SYNTHESIS;

EID: 84921033659     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja5109358     Document Type: Article

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