Temperature and solvent control of the stereoselectivity in the reactions of singlet oxygen with oxazolidinone-substituted enecarbamates

Journal of the American Chemical Society

Volumn 126, Issue 34, 2004, Pages 10498-10499

  Poon, Thomas ^b   Sivaguru, J ^a   Franz, Roberto ^a   Jockusch, Steffen ^a   Martinez, Claudia ^a   Washington, Ilyas ^a   Adam, Waldemar ^c,d   Inoue, Yoshihisa ^e   Turro, Nicholas J ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b KECK GRADUATE INSTITUTE   (United States)

^c UNIVERSITY OF WÜRZBURG   (Germany)

^d UNIVERSITY OF PUERTO RICO   (Puerto Rico)

^e OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID DERIVATIVE; ENECARBAMATE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; SINGLET OXYGEN; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CHIRALITY; CONFORMATIONAL TRANSITION; DIASTEREOISOMER; ENANTIOMER; ENANTIOSELECTIVITY; GEOMETRY; ISOMER; PARAMETER; PHOTOOXIDATION; REACTION ANALYSIS; SOLVENT EFFECT; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS; TEMPERATURE DEPENDENCE;

BENZOIN; CARBAMATES; KINETICS; OXAZOLIDINONES; PHOTOCHEMISTRY; SINGLET OXYGEN; SOLVENTS; STEREOISOMERISM; TEMPERATURE; THERMODYNAMICS;

EID: 4344561898     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja048438c     Document Type: Article

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