Enantioselective Synthesis of Highly Functionalized Phosphonate-Substituted Pyrans or Dihydropyrans Through Asymmetric [4+2] Cycloaddition of β,γ-Unsaturated α-Ketophosphonates with Allenic Esters

Angewandte Chemie - International Edition

Volumn 51, Issue 45, 2012, Pages 11328-11332

  Pei, Cheng Kui ^a   Jiang, Yu ^a   Wei, Yin ^b   Shi, Min ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

asymmetric catalysis; cinchona alkaloids; cycloaddition; dihydropyrans; organocatalysis

Indexed keywords

ASYMMETRIC CATALYSIS; BONDING CHARACTERISTICS; CINCHONA ALKALOID; CYCLOADDITIONS; DIHYDROPYRAN; DIHYDROPYRANS; ENANTIOSELECTIVE SYNTHESIS; FUNCTIONALIZED; HIGH ENANTIOSELECTIVITY; ORGANOCATALYSIS; ORGANOCATALYSTS;

CATALYSIS; ENANTIOSELECTIVITY; ESTERIFICATION; ESTERS; HYDROGEN BONDS; METABOLITES; NITROGEN COMPOUNDS; REACTION KINETICS;

CYCLOADDITION;

ESTER; PHOSPHONIC ACID DERIVATIVE; PYRAN DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLOADDITION; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CYCLOADDITION REACTION; ESTERS; MOLECULAR STRUCTURE; ORGANOPHOSPHONATES; PYRANS; STEREOISOMERISM;

EID: 84868100144     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201206958     Document Type: Article

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