Regioselective and stereospecific cleavage of a terminal oxirane system: A novel synthetic approach to lipid mediator congeners-1,2(2,3)-diacyl-3(1)-halo-sn-glycerols

Bioorganic and Medicinal Chemistry Letters

Volumn 16, Issue 13, 2006, Pages 3388-3391

  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

Diacylglyerols; Glycidol; Lipid mediator

Indexed keywords

1,2(2,3) DIACYL 3(1) HALO SN GLYCEROL DERIVATIVE; ACID ANHYDRIDE; CARBOXYLIC ACID ANYDRIDE; ESTER DERIVATIVE; ETHYLENE OXIDE DERIVATIVE; GLYCEROL DERIVATIVE; GLYCIDYL ESTER; HALIDE; LIPID; TETRA BUTYLAMMONIUM HALIDE; TRIMETHYLSILYL HALIDE; UNCLASSIFIED DRUG;

ARTICLE; RING OPENING; STEREOCHEMISTRY; STEREOSPECIFICITY; SYNTHESIS;

DIGLYCERIDES; ETHYLENE OXIDE; MOLECULAR STRUCTURE; STEREOISOMERISM;

TETRA;

EID: 33646852782     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2006.04.040     Document Type: Article

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34. 4 (508.47): C, 54.33; H, 8.13; I, 24.96%. Found: C, 54.44; H, 8.10; I, 25.00%.