
doi: 10.1007/bf01106667
The Koenigs-Knorr condensation of 1,2- and 2,3-di-O-benzyl-sn-glycerols with acetobromohexapyranoses results in the formation of practically only 1,2-trans-glycosides. The latter have been used for the synthesis of a number of monoglycosyl diglycerides with diglyeride moieties with L and D configurations.
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