The Conformational Behavior of Novel Glycosidase Inhibitors with Substituted Azepan Structures: An NMR and Modeling Study-Reference-Cited by-同舟云学术

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The Conformational Behavior of Novel Glycosidase Inhibitors with Substituted Azepan Structures: An NMR and Modeling Study

Published:2004-10 Issue:20 Volume:2004 Page:4119-4129
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Martínez-Mayorga Karina,Medina-Franco José L.,Mari Silvia,Cañada F. Javier,Rodríguez-García Eliazar,Vogel Pierre,Li Hongqing,Blériot Yves,Sinaÿ Pierre,Jiménez-Barbero Jesús

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Cited by 32 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. Stereoselective Synthesis of Heavily Hydroxylated Azepane Iminosugars via Osmium-Catalyzed Tethered Aminohydroxylation;Organic Letters;2023-07-29

2. Stereoselective Access to Iminosugar C,C-Glycosides from 6-Azidoketopyranoses;Organic Letters;2022-06-22

3. Structural variation of the 3-acetamido-4,5,6-trihydroxyazepane iminosugar through epimerization and C-alkylation leads to low micromolar HexAB and NagZ inhibitors;Organic & Biomolecular Chemistry;2022

4. Contributing to the Study of Enzymatic and Chemical Glycosyl Transfer Through the Observation and Mimicry of Glycosyl Cations;Synthesis;2020-12-03

5. Lewis acid-catalysed nucleophilic opening of a bicyclic hemiaminal followed by ring contraction: Access to functionalized L-idonojirimycin derivatives;Carbohydrate Research;2019-01

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