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- W4238702914 abstract "A novel enzymatic resolution of α-acetoxysulfides has been used as the key step in the synthesis of the important antiviral nucleoside analogue lamivudine. The synthesis proceeds via a configurationally stable hemithioacetal which cyclises in situ to form the required oxathiolane nucleus, which can then be converted into the target nucleoside in 4 steps." @default.
- W4238702914 created "2022-05-12" @default.
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- W4238702914 date "1995-09-18" @default.
- W4238702914 modified "2023-09-26" @default.
- W4238702914 title "Enantioselective Enzymatic Synthesis of the Anti-Viral Agent Lamivudine (3TCTM)." @default.
- W4238702914 doi "https://doi.org/10.1016/00404-0399(50)1380z-" @default.
- W4238702914 hasPublicationYear "1995" @default.
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