Highly diastereoselective dioxetane formation in the photooxygenation of enecarbamates with an oxazolidinone chiral auxiliary: Steric control in the [2 + 2] cycloaddition of singlet oxygen through conformational alignment

Journal of the American Chemical Society

Volumn 124, Issue 30, 2002, Pages 8814-8815

  Adam, Waldemar ^a   Bosio, Sara G ^a   Turro, Nicholas J ^b  

^a UNIVERSITY OF WÜRZBURG   (Germany)

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

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID DERIVATIVE; OXAZOLIDINONE DERIVATIVE;

ARTICLE; CHIRALITY; CONFORMATIONAL TRANSITION; DIASTEREOISOMER; ENANTIOMER; OPTICAL ROTATION; PHOTOOXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; X RAY DIFFRACTION;

EID: 0037205926     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja026815k     Document Type: Article

References (13)