Reaction on d-glucal by an inverting phosphorylase to synthesize derivatives of 2-deoxy-β-d-arabino-hexopyranosyl-(1→4)-d-glucose (2II-deoxycellobiose)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference25 articles.
1. Glycon specificity profiling of α-glucosidases using monodeoxy and mono-O-methyl derivatives of p-nitrophenyl α-d-glucopyranoside
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1. Glycoside phosphorylases: Structure, catalytic properties and biotechnological potential;Biotechnology Advances;2015-03
2. Enzymatic synthesis using glycoside phosphorylases;Carbohydrate Research;2015-02
3. Recent development of phosphorylases possessing large potential for oligosaccharide synthesis;Current Opinion in Chemical Biology;2013-04
4. Examining the role of phosphate in glycosyl transfer reactions of Cellulomonas uda cellobiose phosphorylase using d-glucal as donor substrate;Carbohydrate Research;2012-07
5. Engineering of cellobiose phosphorylase for glycoside synthesis;Journal of Biotechnology;2011-12
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