摘要:
AbstractThis study describes the development of a novel procedure of glycal fluorophosphorylation applied to the synthesis of a fluorinated analogue of an important bacterial metabolite. This procedure was applied to several heptose‐derived glycals, and the stereochemical outcome of the reaction was analyzed. Under optimized conditions, the reaction is β‐gluco selective, but a significant amount of the α‐gluco diastereomer is also generated.