Broadening the reaction scope of unprotected aldosesviatheir corresponding nitrones: 1,3-dipolar cycloadditions with alkenes-Reference-Cited by-同舟云学术

Broadening the reaction scope of unprotected aldosesviatheir corresponding nitrones: 1,3-dipolar cycloadditions with alkenes

Published:2020 Issue:29 Volume:18 Page:5708-5725
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Messire Gatien¹²³⁴⁵,Massicot Fabien¹²³⁴⁵^ORCID,Pascual Laura¹²³⁴⁵,Riguet Emmanuel¹²³⁴⁵^ORCID,Vasse Jean-Luc¹²³⁴⁵^ORCID,Behr Jean-Bernard¹²³⁴⁵^ORCID

Affiliation:

1. Univ. Reims Champagne-Ardenne

2. ICMR

3. CNRS UMR 7312

4. FR Condorcet CNRS 3417

5. 51687 Reims Cedex 2

Abstract

Condensation reactions of unprotected tetroses and pentoses with hydroxylamines afforded nitrones, which were easily converted to densely functionalized isoxazolidines in the presence of electron-poor alkenes.

Funder

Centre National de la Recherche Scientifique

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01350A

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