A comparative mechanistic analysis of the stereoselectivity trends observed in the oxidation of chiral oxazolidinone-functionalized enecarbamates by singlet oxygen, ozone, and triazolinedione

Tetrahedron

Volumn 62, Issue 46, 2006, Pages 10647-10659

  Sivaguru, J ^a   Poon, Thomas ^b   Hooper, Catherine ^b   Saito, Hideaki ^a,c,d   Solomon, Marissa R ^a   Jockusch, Steffen ^a   Adam, Waldemar ^e,f   Inoue, Yoshihisa ^c,d   Turro, Nicholas J ^a,g  

^a Howard Hughes Medical Institute   (United States)

^b KECK GRADUATE INSTITUTE   (United States)

^c OSAKA UNIVERSITY   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^e UNIVERSITY OF WÜRZBURG   (Germany)

^f UNIVERSITY OF PUERTO RICO RIO PIEDRAS   (Puerto Rico)

^g Fu Foundation School of Engineering and Applied Science   (United States)

Author keywords

Kinetic resolution; Ozonolysis; Photooxygenation; Solvent and temperature effects; Substituent; Vibrational quenching

Indexed keywords

BENZOIN; CARBAMIC ACID DERIVATIVE; OXAZOLIDINONE DERIVATIVE; OXIDIZING AGENT; OZONE; SINGLET OXYGEN; SOLVENT; TRIAZOLINE DERIVATIVE;

ARTICLE; CHEMICAL REACTION KINETICS; CHIRALITY; COMPARATIVE STUDY; ENANTIOMER; OXIDATION KINETICS; PRIORITY JOURNAL; STEREOCHEMISTRY; STEREOSPECIFICITY; TEMPERATURE DEPENDENCE;

EID: 33749362970     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.105     Document Type: Article

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