Ab initio study of the (5R)- and (5S)-TT pyrimidine h5(6-4) pyrimidone photoproducts. Implications on the design of new biologically relevant analogues

Journal of Organic Chemistry

Volumn 67, Issue 26, 2002, Pages 9140-9145

  Dupradeau, François Yves ^c   Sonnet, Pascal ^c   Guillaume, Dominique ^c   Senn, Hans Martin ^b   Clivio, Pascale ^a  

^a CNRS   (France)

^b UNIVERSITY OF CALGARY   (Canada)

^c GRBPD   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DERIVATIVES; FREE ENERGY; ISOMERS; VAN DER WAALS FORCES;

DIASTREOMERS;

ORGANIC COMPOUNDS;

1,6 DIMETHYL 5,6 DIHYDROTHYMINE; PYRIMIDINE; PYRIMIDINONE DERIVATIVE; THYMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CONFORMATION; ENERGY TRANSFER; ISOMER; PREDICTION; THEORY;

COMPUTATIONAL BIOLOGY; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PHOTOCHEMISTRY; PYRIMIDINES; PYRIMIDINONES; STEREOISOMERISM; THERMODYNAMICS;

EID: 0142029777     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo020604g     Document Type: Article

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