Kinetically controlled nucleophilic addition-reactions to methyl 4,6-O-benzylidene-2,3-dideoxy-2-nitro-α-d-erythro-hex-2-enopyranoside
- 1 August 1984
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 131 (2) , 197-208
- https://doi.org/10.1016/0008-6215(84)85241-6
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- SYNTHESIS OF ULOSES BY THE OXIDATION WITH DIMETHYL SULFOXIDE-TRIFLUOROACETIC ANHYDRIDEChemistry Letters, 1977
- 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 interactionThe Journal of Organic Chemistry, 1977
- A study of non-bonded interactions of nitro and nitronate substituents in inositolsCanadian Journal of Chemistry, 1976
- Steric and electrostatic interactions in reactions of carbohydrates. II. Stereochemistry of addition reactions to the carbonyl group of glycopyranosiduloses. Synthesis of methyl 4,6-O-benzylidene-3-O-methyl .beta.-D-mannopyranosideThe Journal of Organic Chemistry, 1974
- 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-enopyranosidesJournal of the Chemical Society, Perkin Transactions 1, 1972
- Alkaline Epoxidation of Carbohydrate NitroolefinsCanadian 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-glucopyranosideBulletin of the Chemical Society of Japan, 1970
- Allylic strain in six-membered ringsChemical Reviews, 1968
- Peroxytrifluoroacetic Acid. VI. The Oxidation of Oximes to Nitroparaffins1,2Journal of the American Chemical Society, 1955