Beyond classical reactivity patterns: Shifting from 1,4- to 1,6-additions in regio- and enantioselective organocatalyzed vinylogous reactions of olefinic lactones with enals and 2,4-dienals

Journal of the American Chemical Society

Volumn 135, Issue 21, 2013, Pages 8063-8070

  Dell'Amico, Luca ^a   Albrecht, Łukasz ^a   Naicker, Tricia ^a   Poulsen, Pernille H ^a   Jørgensen, Karl Anker ^a  

^a AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

CONJUGATE ADDITION REACTIONS; ENANTIOSELECTIVE; GEOMETRY CONTROLS; OPTICALLY ACTIVE; ORGANOCATALYSTS; REACTION CONCEPT; REACTIVITY PATTERN; SITE SELECTIVITY;

ADDITION REACTIONS; CATALYSTS; ESTERS; REACTION KINETICS;

ENANTIOSELECTIVITY;

2,4 DIENAL DERIVATIVE; ALDEHYDE DERIVATIVE; ENAL DERIVATIVE; LACTONE DERIVATIVE; OLEFINIC AZLACTONE DERIVATIVE; OLEFINIC BUTYROLACTONE DERIVATIVE; OLEFINIC LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CATALYSIS; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; ENANTIOSELECTIVITY; ISOMERISM; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 84878397638     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4029928     Document Type: Article

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