Enecarbamates as Selective Substrates in Oxidations: Chiral-Auxiliary-Controlled Mode Selectivity and Diastereoselectivity in the [2+2] Cycloaddition and Ene Reaction of Singlet Oxygen and in the Epoxidation by DMD and mCPBA

Journal of Organic Chemistry

Volumn 69, Issue 5, 2004, Pages 1704-1715

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

^a UNIVERSITY OF WÜRZBURG   (Germany)

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

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CHEMICAL BONDS; NITROGEN COMPOUNDS; OXIDATION; OXYGEN; STEREOCHEMISTRY;

SELECTIVE SUBSTRATES; STEREOELECTRONIC STEERING;

ORGANIC COMPOUNDS;

3 CHLOROPERBENZOIC ACID; CARBAMIC ACID DERIVATIVE; DIMETHYLDIOXIRANE; ENECARBAMATE; SINGLET OXYGEN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CYCLOADDITION; EPOXIDATION; OXIDATION; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 1442275451     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035745c     Document Type: Article

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