Issue 47, 2017, Issue in Progress

Lewis base-catalyzed diastereoselective [3 + 2] cycloaddition reaction of nitrones with electron-deficient alkenes: an access to isoxazolidine derivatives

Abstract

A Lewis base-catalyzed [3 + 2] cycloaddition reaction of nitrones with electron-deficient alkenes has been achieved under mild reaction conditions, affording various functionalized isoxazolidine derivatives as single diastereomers in moderate to excellent yields.

Graphical abstract: Lewis base-catalyzed diastereoselective [3 + 2] cycloaddition reaction of nitrones with electron-deficient alkenes: an access to isoxazolidine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
15 Apr 2017
Accepted
31 May 2017
First published
06 Jun 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 29515-29519

Lewis base-catalyzed diastereoselective [3 + 2] cycloaddition reaction of nitrones with electron-deficient alkenes: an access to isoxazolidine derivatives

H. Liu, Y. Zhao, Z. Li, H. Jia, C. Zhang, Y. Xiao and H. Guo, RSC Adv., 2017, 7, 29515 DOI: 10.1039/C7RA04264G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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