(1′R,2′S,5′R)-Menthyl-(5R)-acetoxy-1,3-oxathiolan-(2R)-carboxylate: Synthesis and isomeric purity determination by HPLC |
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Authors: | M. Arshad Siddiqui Haolun Jin Colleen A. Evans Marika P. Dimarco H. L. Allan Tse Tarek S. Mansour |
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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. |
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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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