Synthèse d'oligosaccharides sur polymère support : Partie III. Possibilités d'utilisation du groupe chloroacétyle pour la protection de la position 6 de derivés du D-glucose
- 31 May 1973
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 28 (1) , 165-170
- https://doi.org/10.1016/s0008-6215(00)82877-3
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Solid-phase synthesis of oligosaccharides. II. Synthesis of 2-acetamido-6--(2-acetamido-2-deoxy-β--glucopyranosyl)-2-deoxy--glucose.Tetrahedron Letters, 1972
- Removal of the Chloroacetyl Group from N‐Chloroacetyl Derivatives of Amino Acids and Peptides by Means of 1‐PiperidinethiocarboxamideAngewandte Chemie International Edition in English, 1971
- The chloroacetyl group in synthetic carbohydrate chemistryCarbohydrate Research, 1970
- Relative reactivities of hydroxyl groups in carbohydrate derivatives. Specific NMR spectral assignments of acetyl groups in methyl tetra-O-acetyl-.alpha.-D-glucopyranoside and related derivativesThe Journal of Organic Chemistry, 1969
- Determination of the Position of the Xanthate Groups in Glucopyranosides by Means of Nuclear Magnetic Resonance. Part 1. Position of the Xanthate Group in Mono-S-methyl Xanthates of Methyl D-Glucopyranosides.Acta Chemica Scandinavica, 1966
- The Preparation of α- and β-Gentiobiose OctaacetatesJournal of the American Chemical Society, 1938