An approach to regioselective alkylation of alkyl β-d-galactopyranosides through (trialkylstannyl)ation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference20 articles.
1. Regioselective enhancement of the nucleophilicity of hydroxyl groups through trialkylstannylation: a route to partial alkylation of polyhydroxy compounds
2. Studies in oligosaccharide chemistry. Part 8. Synthesis of lacto-N-triose I, a core chain trisaccharide of human blood-group substances
3. Synthesis of a branched pentasaccharide: one of the core oligosaccharides of human blood-group substances
4. Chemical modification of lactose. XIV. Synthesis of O-2-acetamido-2-deoxy-.BETA.-D-glucopyranosyl-(1.RAR.3)-O-(2-acetamido-2-deoxy-.BETA.-D-glucopyranosyl-(1.RAR.6))-O-.BETA.-D-galactopyranosyl-(1.RAR.4)-.BETA.-D-glucopyranose (3',6'-Di-.BETA.-N-acetylglucosaminyl-.BETA.-lactose).
5. Hydrogenolysis of the dioxolan type - and - benzylidene derivatives of carbohydrates with the LiAlH4-AlCl3 reagent
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