Efficient, highly regioselective, and stereospecific conversion of glycidol systems into C2-O-acylated vicinal halohydrins

Tetrahedron Letters

Volumn 47, Issue 15, 2006, Pages 2543-2547

  Stamatov, Stephan D ^a   Stawinski, Jacek ^b,c  

^a UNIVERSITY OF PLOVDIV   (Bulgaria)

^b STOCKHOLM UNIVERSITY   (Sweden)

^c INSTITUTE OF BIOORGANIC CHEMISTRY   (Poland)

Author keywords

Carboxylic acids; Glycidol; Trifluoroacetic anhydride; Trimethylsilyl halides; Vicinal haloesters

Indexed keywords

2 O ACYLHALOHYDRIN; ACID ANHYDRIDE; CARBOXYLIC ACID; CHLOROFORM; ESTER; ETHER; ETHYLENE OXIDE; GLYCIDOL; HALIDE; PYRIDINE; TRIFLUOROACETIC ACID; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; OXIDATION; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 33644885268     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.02.050     Document Type: Article

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