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• W2016132541 abstract "A new efficient chemoenzymatic methodology for the production of 3-O-benzyl-sn-glycerol and 1,2-O-dipalmitoyl-sn-glycerol has been developed. It starts from racemic 1-O-benzylglycerol and is based on the sequential enzymatic acylation––Mitsunobu inversion––enzymatic hydrolysis, which has been performed without isolation of the intermediates. In this way a 70–75% yield of 3-O-benzyl-sn-glycerol with 94–96% ee has been obtained." @default.
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• W2016132541 date "2004-09-01" @default.
• W2016132541 modified "2023-10-16" @default.
• W2016132541 title "Efficient chemoenzymatic enantioselective synthesis of diacylglycerols (DAG)" @default.
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• W2016132541 doi "https://doi.org/10.1016/j.tetasy.2004.07.040" @default.
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