Synthesis and evaluation of diastereoisomeric alkylating pseudo-disaccharides as potential affinity reagents for trehalase
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference18 articles.
1. Stereochemistry of the hydrolysis of α,α-trehalose by trehalase, determined by using a labelled substrate
2. Reactive pseudo-oligosaccharides as potential irreversible inhibitors for sugar-binding proteins: synthesis of the diastereoisomers of (3,4,6/5)-3,4-epoxy-6-(β-d-galactopyranosyl-thio)-5-hydroxycyclohexene
3. Irreversible Desaktivierung von menschlicher β-Hexosaminidase A mit dem alkylierenden Pseudodisaccharid (3,4,6/5)-6-(2-Acetamido-2-desoxy-β-D-glucopyranosylthio)-3,4-epoxy-5-hydroxycyclohexen
4. Trehalase: stereocomplementary hydrolytic and glucosyl transfer reactions with .alpha.- and .beta.-D-glucosyl fluoride
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