Synthesis of new N-substituted 3,4,5-trihydroxypiperidin-2-ones from d-ribono-1,4-lactone-Reference-Cited by-同舟云学术

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Synthesis of new N-substituted 3,4,5-trihydroxypiperidin-2-ones from d-ribono-1,4-lactone

Published:2010-09 Issue:14 Volume:345 Page:1983-1987
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Falentin-Daudre Céline,Beaupère Daniel,Stasik-Boutbaiba Imane

Funder

Ministère de la Recherche

Conseil Régional de Picardie

CNRS

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference49 articles.

1. Structure and synthesis of nojirimycin

2. Deoxynojirimycin: synthesis and biological activity

3. Total synthesis of (+)-α-homonojirimycin

4. Nitrogen-in-the-Ring Pyranoses and Furanoses: Structural Basis of Inhibition of Mammalian Glycosidases

5. Iminosugars as Glycosidase Inhibitors: Nojirimycin and Beyond;Stütz,1999

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1. Explaining the persistence of hazardous chemicals in the Doce River (Brazil) by multiple sources of contamination and a major environmental disaster;Journal of Hazardous Materials Advances;2023-02

2. Fast and Efficient Mechanosynthesis of Aldonamides by Aminolysis of Unprotected Sugar Lactones;Sustainable Chemistry;2022-06-22

3. D-Ribonolactone, A Versatile Synthetic Precursor of Biologically Relevant Scaffolds;Current Organic Synthesis;2015-08-21

4. N-Arylated-Lactam-Type Iminosugars as New Immunosuppressive Agents: Discovery, Optimization, and Biological Evaluation;Chemistry - An Asian Journal;2014-04-02

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