Synthesis of 1,5-Dideoxy-1,5-iminoribitol C-Glycosides through a Nitrone–Olefin Cycloaddition Domino Strategy: Identification of Pharmacological Chaperones of Mutant Human Lysosomal β-Galactosidase-Reference-Cited by-同舟云学术

Synthesis of 1,5-Dideoxy-1,5-iminoribitol C-Glycosides through a Nitrone–Olefin Cycloaddition Domino Strategy: Identification of Pharmacological Chaperones of Mutant Human Lysosomal β-Galactosidase

Published:2014-04-28 Issue:10 Volume:79 Page:4398-4404
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Siriwardena Aloysius¹,Sonawane Dhiraj P.,Bande Omprakash P.¹,Markad Pramod R.,Yonekawa Sayuri²,Tropak Michael B.²,Ghosh Sougata,Chopade Balu A.,Mahuran Don J.²,Dhavale Dilip D.

Affiliation:

1. Laboratoire de Glycochimie, des Antimicrobiens et des Agroressources, Université de Picardie Jules Verne, FRE 3517 CNRS, Amiens 80039, France

2. Programme in Genetics and Genome Biology, Sickkids, Toronto, Ontario M5G 1X8, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500328u

Reference49 articles.

1. Iminosugars

2. Amino-sugar glycosidase inhibitors: versatile tools for glycobiologists

3. Isofagomine, a Potent, New Glycosidase Inhibitor

4. Carbohydrate mimetics-based glycosyltransferase inhibitors

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