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(1′R,2′S,5′R)-Menthyl-(5R)-acetoxy-1,3-oxathiolan-(2R)-carboxylate: Synthesis and isomeric purity determination by HPLC
Authors:M. Arshad Siddiqui  Haolun Jin  Colleen A. Evans  Marika P. Dimarco  H. L. Allan Tse  Tarek S. Mansour
Abstract:Chemoselective reduction of one isomer of the 1-menthylester of 1,3-oxathiolan-5-one-2-carboxylic acid produces a mixture of four lactol diastereomers from which the title compound was isolated after acylation. The isomeric purity and absolute stereochemistry were determined by spectroscopic methods, chiral HPLC techniques, and conversion to (?)-2′-deoxy-3′-thiacytidine (Lamivudine, 3TCTM). © 1994 Wiley-Liss, Inc.
Keywords:chemoselective reduction  disiamylborane  (−  )-2′  -deoxy-3′  -thiacytidine  (1′  R,2′  S,5′  R)-menthyl-(5R)-acetoxy-1,3-oxathiolan-(2R)-carboxylate  Lamivudine  3TCTM  chiral HPLC  chiral stationary phase  Pirkle β  -GEM 1 column
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