Enzymatic synthesis of nucleoside analogues from uridines and vinyl esters in a continuous-flow microreactor
Li-Hua Du1, Jia-Hong Shen1, Zhen Dong1
1College of Pharmaceutical Science, Zhejiang University of Technology Hangzhou 310014 China orgdlh@zjut.edu.cn orgdlh@gmail.com +86 571 88320903.
Abstract:
We achieved the effective controllable regioselective acylation of the primary hydroxyl group of uridine derivatives catalyzed by Lipase TL IM from Thermomyces lanuginosus with excellent conversion and regioselectivity. Various reaction parameters were studied. These regioselective acylations performed in continuous flow microreactors are a proof-of-concept opening the use of enzymatic microreactors in uridine derivative biotransformations.
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