Concise and Highly Stereocontrolled Synthesis of 1-Deoxygalactonojirimycin and Its Congeners Using Dioxanylpiperidene, a Promising Chiral Building Block-Reference-Cited by-同舟云学术

Concise and Highly Stereocontrolled Synthesis of 1-Deoxygalactonojirimycin and Its Congeners Using Dioxanylpiperidene, a Promising Chiral Building Block

Published:2003-06-19 Issue:14 Volume:5 Page:2527-2529
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Takahata Hiroki¹,Banba Yasunori¹,Ouchi Hidekazu¹,Nemoto Hideo¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Tohoku Pharmaceutical University, Sendai 981-8558, Japan, and Faculty of Pharmaceutical Sciences, Toyama Medical & Pharmaceutical University, Toyama 930-0194, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol034886y

Reference18 articles.

1. Recent Insights into Inhibition, Structure, and Mechanism of Configuration-Retaining Glycosidases

2. Asymmetric routes to azasugars from chiral bicyclic lactams. Synthesis of 1,4-dideoxy-1,4-imino-D-lyxitol; L-deoxymannojirimycin; rhammo-1-deoxynojirimycin and 1-deoxy-6-epicastanospermine

3. Inhibition of Glycosphingolipid Biosynthesis: Application to Lysosomal Storage Disorders

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