[1,4]-sigmatropic rearrangement of chiral nitrones and their utilization in the synthesis of new iminosugars-Reference-Cited by-同舟云学术

[1,4]-sigmatropic rearrangement of chiral nitrones and their utilization in the synthesis of new iminosugars

Published:2016 Issue:2 Volume:14 Page:470-482
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Malinowski Maciej¹²³⁴,Rowicki Tomasz¹²³⁴,Guzik Patrycja¹²³⁴,Gryszel Maciej¹²³⁴,Łapczyński Sebastian¹²³⁴,Wielechowska Monika¹²³⁴,Czerwińska Karolina¹²³⁴,Madura Izabela¹²³⁴,Sas Wojciech¹²³⁴

Affiliation:

1. Faculty of Chemistry

2. Warsaw University of Technology

3. 00-664 Warsaw

4. Poland

Abstract

A new mechanism of nitrone epimerization via [1,4]-sigmatropic rearrangement was proposed and a set of epimeric iminosugars was synthesized.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C5OB01432H

Reference101 articles.

1. Therapeutic Applications of Iminosugars: Current Perspectives and Future Opportunities

2. Iminosugars as therapeutic agents: recent advances and promising trends

3. Imino sugar glucosidase inhibitors as broadly active anti-filovirus agents

4. Iminosugars as Immunomodulating Agents: Synthesis and Biological Activities of 1-Deoxynojirimycin and Related Compounds

5. Natural and Synthetic Iminosugars as Carbohydrate Processing Enzyme Inhibitors for Cancer Therapy

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