Novel glycosylation reagents: synthesis of disaccharides containing 2-deoxy-2-iodo-α-d-talopyranosyl groups
✍ Scribed by Per J. Garegg; Bertil Samuelsson; Peter Konradsson; Ingemar Kvarnström; Stefan C.T. Svensson
- Book ID
- 108308872
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 216 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0008-6215
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📜 SIMILAR VOLUMES
1999 carbohydrates carbohydrates U 0500 47 -218 2-Deoxy-2-iodo-α-mannopyranosyl and -talopyranosyl Acetates: Highly Stereoselective Glycosyl Donors for the Synthesis of 2-Deoxyα-glycosides. -Reactions of the title compounds with various glycosyl acceptors in the presence of TmsOTf are found to yiel
Addition oP C,F'-dialkylphosphorodithioic acids to fully protected 1,2-unsaturated hsxo-and pentopyranoses gives S-(2-deoxy-glycosyl)-phosphorodithioates 'P -OH RO' 'SH -# H /OR HS-l'OR 2 2 Scheme I 2oa the &\_-adducte. The observed Oc'/s ratio was 89:ll and 92:8, respectively. pllso in these cases
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