Asymmetric Synthesis of Polyhydroxylated N-Alkoxypiperidines by Ring-Closing Double Reductive Amination: Facile Preparation of Isofagomine and Analogues-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Polyhydroxylated N-Alkoxypiperidines by Ring-Closing Double Reductive Amination: Facile Preparation of Isofagomine and Analogues

Published:2011-12-23 Issue:2 Volume:14 Page:596-599
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Malik Gaëlle¹²,Guinchard Xavier¹²,Crich David¹²

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, CNRS, Avenue de la Terrasse, 91198 Gif-sur-Yvette, France

2. Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol203213f

Reference37 articles.

1. Synthesis of isofagomine, a novel glycosidase inhibitor

2. Novel Hybrid Morpholino-Glycopeptides with the Amino Acid Nitrogen Replacing C-3 of the Pyranose Ring

3. Design and synthesis of 2-acetamidomethyl derivatives of isofagomine as potential inhibitors of human lysosomal β-hexosaminidases

4. Syntheses with anhydro sugars. V. Preparation of 2,4-di-O-substituted 1,6-anhydro-β-D-hexopyranos-3-uloses and their isomerization and reduction

5. A facile synthesis of Cerny epoxides and selectively blocked derivatives of 2-azido-2-deoxy-β-d-glucopyranose

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