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Journal of the American Chemical Society

Volumn 124, Issue 27, 2002, Pages 7982-7990

Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: Host-guest interactions, product configuration, and the origin of the stereoselectivity in solution

(4) Bach, Thorsten a Bergmann, Hermann b,c Grosch, Benjamin a Harms, Klaus b

a TECHNICAL UNIVERSITY OF MUNICH (Germany)

b PHILIPPS UNIVERSITY MARBURG (Germany)

c UNIVERSITY OF CAMBRIDGE (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PHOTOCYCLOADDITION;

HYDROGEN; OLEFINS; PHOTOCHEMICAL REACTIONS; SOLVENTS; TOLUENE;

CHEMICAL ANALYSIS;

2 QUINOLONE DERIVATIVE; ALKENE; LACTAM; QUINOLONE DERIVATIVE; STYRENE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CYCLOADDITION; ENANTIOSELECTIVITY; HYDROGEN BOND; MOLECULAR INTERACTION; PHOTOCHEMISTRY; STEREOCHEMISTRY; TITRIMETRY; X RAY CRYSTALLOGRAPHY;

EID: 0037055113 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja0122288 Document Type: Article

Times cited : (193)

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