Synthesis and ring-opening reactions of 4-chloro-4-deoxy-α-d-galactopyranosyl 3,4-anhydro-1,6-dichloro-1,6-dideoxy-β-d-lyxo-hexulofuranoside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference10 articles.
1. Cyclic acetals of 4,1′,6′-trichloro-4,1′,6′-trideoxy-galacto-sucrose and their conversion into methyl ether derivatives
2. Synthesis of sucrose epoxides, partial de-esterification of 1′,2:4,6-di-O-isopropylidenesucrose tetra-acetate, and selective tosylation of 3,6′-di-O-acetyl-1′,2:4,6-di-O-isopropylidenesucrose
3. Ring-opening reactions of sucrose epoxides: Synthesis of 4′-derivatives of sucrose
4. Reaction of methanesulphonyl chloride-N,N-dimethylformamide with partially esterified derivatives of sucrose
5. Derivatives of β-D-fructofuranosyl α-D-galactopyranoside
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2. Some studies on the selective synthesis of sucrose acetates using template and random trityl chloride functionalised macroporous polymers;Carbohydrate Research;1996-08
3. Halogenation reactions of derivatives ofd-glucose and sucrose;Carbohydrate Research;1990-09
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