Efficient synthesis of (+)-1,8,8a-tri-epi-swainsonine, (+)-1,2-di-epi-lentiginosine, (+)-9a-epi-homocastanospermine and (−)-9-deoxy-9a-epi-homocastanospermine from a d-glucose-derived aziridine carboxylate, and study of their glycosidase inhibitory activities-Reference-Cited by-同舟云学术

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Efficient synthesis of (+)-1,8,8a-tri-epi-swainsonine, (+)-1,2-di-epi-lentiginosine, (+)-9a-epi-homocastanospermine and (−)-9-deoxy-9a-epi-homocastanospermine from a d-glucose-derived aziridine carboxylate, and study of their glycosidase inhibitory activities

Published:2008 Issue:4 Volume:6 Page:703
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Ajish Kumar K. S.,Chaudhari Vinod D.,Dhavale Dilip D.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2008/OB/B712753G

Reference112 articles.

1. Advances in Nitrogen Transfer Reactions Involving Aziridines

2. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

3. Bi(OTf)3-[Bmim]PF6:A novel and Reusable Catalytic System for the Synthesis ofcis -AziridineCarboxylates

4. The Synthetic Potential of Three-Membered Ring Aza-Heterocycles

5. Aziridines: epoxides’ ugly cousins?

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4. A divergent entry to 1,2,3,9-tetrahydroxyquinolizidines;Tetrahedron Letters;2020-06

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