Stereoselective nucleophilic addition reactions to nitro sugars

This publication has 8 references indexed in Scilit:

• The Michael reaction of a methyl 2-C-nitro-α-d-hex-2-enopyranoside: Preparation and structural determination of the adducts having the d-altro-, d-gluco, and d-manno configurations
  Carbohydrate Research, 1981
• Synthesis, stereochemistry, and epimerization of methyl 4,6-O-benzylidene-2,3-dicyano-2,3-dideoxy-β-D-hexopyranosides having the allo, altro, gluco, and manno configurations
  Carbohydrate Research, 1980
• Stereochemistry of nucleophilic addition reactions. 2. Kinetically controlled reaction of methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-.beta.-D-erythro-hex-2-enopyranoside with hydrogen cyanide. Important role of electrostatic interaction
  The Journal of Organic Chemistry, 1977
• Arylazo-glycenosides. Part I. Synthesis and reactions of some 2- and 3-arylazo-derivatives of methyl 4,6-O-benzylidene-2,3-dideoxy-D-hex-2-enopyranosides
  Journal of the Chemical Society, Perkin Transactions 1, 1972
• Alkaline Epoxidation of Carbohydrate Nitroolefins
  Canadian Journal of Chemistry, 1971
• Preparation of Methyl 2,3-Anhydro-4,6-O-benzylidene-3-deoxy-3-nitro-β-d-allopyranoside and Some C2-Branched-Chain Derivatives of Methyl 4,6-O-Benzylidene-2,3-dideoxy-3-nitro-β-d-glucopyranoside
  Bulletin of the Chemical Society of Japan, 1970
• Allylic strain in six-membered rings
  Chemical Reviews, 1968
• Steric Interference in Allylic and Pseudo-Allylic Systems. I. Two Stereochemical Theorems
  Journal of the American Chemical Society, 1965