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Stereoselective nucleophilic addition reactions to nitro sugars
Authors:Tohru Sakakibara      Yoshifusa Tachimori  Rokuro Sudoh
Affiliation:

Department of Chemistry, Faculty of Science, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152, Japan

Abstract:Nucleophile(s) almost exclusively added from the equatorial side of 2-nitro-β-D-2-enopyranoside and the axial side of 2-nitro-D-ribo-1-enitol. On the other hand, methoxide and tert-butyl peroxide ions approached from the equatorial side of 2-nitro-α-D-2-enopyranoside, whereas methanol and hydrogen peroxide ion from the axial side.
Keywords:
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