Issue 12, 1991

Synthesis of trifluoromethyl analogue of L-fucose and 6-deoxy-D-altrose

Abstract

Trifluoromethylation of the acyclic derivative of D-lyxose, 3, with trifluoromethyltrimethylsilane in the presence of tetrabutylammonium fluoride yielded a mixture of trifluoromethyl adducts, 5a and b, which was converted to 6,6,6-trifluoro-L-fucose 9a and 6-deoxy-6,6,6-trifluoro-D-altrose 9bvia selective oxidation of the primary hydroxy group involving treatment of the trimethylsiloxy derivatives, 7a and b, with Collins reagent.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 796-798

Synthesis of trifluoromethyl analogue of L-fucose and 6-deoxy-D-altrose

R. C. Bansal, B. Dean, S. Hakomori and T. Toyokuni, J. Chem. Soc., Chem. Commun., 1991, 796 DOI: 10.1039/C39910000796

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