科研之友
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摘要
Novel thiomannosyl donors with a 2,3-(phenyl-1,2-ethylidine) tethering group were designed so that the phenyl group would act as a molecular lever and force the pyranoside into its most reactive conformation. It was demonstrated that this type of molecular leverage could increase the reaction rate at least 200 times.
- 出版日期2016-1-6
