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• W2003676229 abstract "Glycidyl esters upon treatment with a mixture of carboxylic acid anhydride (CAA) and trimethylsilyl halide (TMSX) in the presence of tetra-n-butylammonium halide (Bu(4)NX, X=Cl, Br or I) undergo stereospecific and regioselective opening of the oxirane ring to afford mixed-(or mono)-acid 1,2(2,3)-diacyl-3(1)-halo-sn-glycerols in high yields." @default.
• W2003676229 created "2016-06-24" @default.
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• W2003676229 date "2006-07-01" @default.
• W2003676229 modified "2023-10-13" @default.
• W2003676229 title "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" @default.
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• W2003676229 doi "https://doi.org/10.1016/j.bmcl.2006.04.040" @default.
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