Cyclohexane‐1,2‐diacetals (CDA): A New Protecting Group for Vicinal Diols in Carbohydrates
- 5 December 1994
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 33 (22) , 2290-2292
- https://doi.org/10.1002/anie.199422901
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Dispiroketals in synthesis (part 7): Protection of D-glucopyranose substratesTetrahedron Letters, 1994
- A Facile One‐Pot Synthesis of a Trisaccharide Unit from the Common Polysaccharide Antigen of Group B Streptococci Using Cyclohexane‐1, 2‐diacetal (CDA) Protected RhamnosidesAngewandte Chemie International Edition in English, 1994
- Eintopfsynthese einer Trisaccharideinheit des gemeinen Polysaccharid‐Antigens von Streptococci der Gruppe B unter Verwendung Cyclohexan‐1,2‐diacetal(CDA)‐geschützter RhamnosideAngewandte Chemie, 1994
- Dispiroketals in synthesis (Part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptorsTetrahedron Letters, 1993
- Syntheses of the octyl and tetradecyl glycosides of 3,6-di-O-α-d-mannopyranosyl-α-d-mannopyranose and of 3,4-di-O-α-d-mannopyranosyl-α-d-mannopyranose. A new way for 2,4-di-O-protection of mannopyranosidesCarbohydrate Research, 1993
- Dispiroketals in Synthesis (Part 3):1Selective Protection of Diequatorial Vicinal Diols in CarbohydratesSynthesis, 1993
- Dispiroketals in synthesis (part 2): A new group for the selective protection of diequatorial vicinal diols in carbohydrates.Tetrahedron Letters, 1992
- Synthetic oligosaccharides related to Group B streptococcal polysaccharides. The rhamnotriose moiety of the common antigenCanadian Journal of Chemistry, 1987
- Assignment of ring size in isopropylidene acetals by 13C N.M.R.Tetrahedron Letters, 1980
- Monomolar acetalations of methyl α-d-mannosides—synthesis of methyl α-d-talopyranosideCarbohydrate Research, 1977