Aza-Claisen rearrangement of 2-C-hydroxymethyl glycals as a versatile strategy towards synthesis of isofagomine and related biologically important azasugars-Reference-Cited by-同舟云学术

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Aza-Claisen rearrangement of 2-C-hydroxymethyl glycals as a versatile strategy towards synthesis of isofagomine and related biologically important azasugars

Published:2012 Issue:14 Volume:10 Page:2760
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Reddy Y. Suman,Kancharla Pavan K.,Roy Rashmi,Vankar Yashwant D.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB06851F

Reference53 articles.

1. Sugar-mimicking glycosidase inhibitors: bioactivity and application

2. Recent advances in the chemistry of azapyranose sugars

3. Recent Advances in the Total Synthesis of Piperidine Azasugars

4. Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application

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1. A concise synthetic approach for isoiminosugars;Carbohydrate Research;2024-10

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3. Synthesis of Fluorinated Amides Starting from Carbohydrates Based on the Claisen Rearrangement;European Journal of Organic Chemistry;2022-01-14

4. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances;Russian Chemical Reviews;2022

5. Cyclisations and Strategies for Stereoselective Synthesis of Piperidine Iminosugars;The Chemical Record;2021-10-28

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