Support of a cyclic versus acyclic intermediate in enzymatic glycoside cleavage: 1,3-(R)-O-benzylidene-d-threitol is a competitive inhibitor but not a substrate of β-d-galactosidase-Reference-Cited by-同舟云学术

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Support of a cyclic versus acyclic intermediate in enzymatic glycoside cleavage: 1,3-(R)-O-benzylidene-d-threitol is a competitive inhibitor but not a substrate of β-d-galactosidase

Published:1995-10 Issue:1 Volume:276 Page:215-218
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Lehmann Jochen,Wagenknecht Hans-Achim

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference12 articles.

1. Reaktionen enolischer zuckerderivate

2. Scope and mechanism of carbohydrase action: stereospecific hydration of D-glucal catalyzed by α- and β-glucosidase

3. The conversion of 2,6-anhydro-1-deoxy-d-galacto-hept-1-enitol into 1-deoxy-d-galacto-heptulose by β-d-galactosidase

4. Reaktionen enolischer Zuckerderivate, VII1) Die Wirkung von β-Galaktosidase aufo-Nitrophenyl-6-desoxy-α-L-Δ5-arabinohexenopyranosid. Enzymatische Synthese von 1′-D-Glyceryl-6-desoxy-α-L-Δ5-arabinohexenopyranosid

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Dioxanone Approach to (2S,3R)-2-C-Methylerythritol 4-Phosphate and 2,4-Cyclodiphosphate, and Various MEP Analogues;The Journal of Organic Chemistry;2007-11-17

2. Synthesis of Enantiopure 2-C-Methyl-d-erythritol 4-Phosphate and 2,4-Cyclodiphosphate from d-Arabitol;Organic Letters;2003-12-09

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