Issue 87, 2017, Issue in Progress

1,3-Dipolar [3 + 3] cycloaddition of α-halohydroxamate-based azaoxyallyl cations with hydrazonoyl chloride-derived nitrile imines

Abstract

Promoted by Et3N, the 1,3-dipolar [3 + 3] cycloaddition of α-halohydroxamate-based azaoxyallylcations with hydrazonoyl chloride-derived nitrile imines occurred efficiently, and furnished desired products in acceptable chemical yields. The chemical structure of the title compounds was firmly confirmed by an X-ray single crystal structure analysis.

Graphical abstract: 1,3-Dipolar [3 + 3] cycloaddition of α-halohydroxamate-based azaoxyallyl cations with hydrazonoyl chloride-derived nitrile imines

Supplementary files

Article information

Article type
Paper
Submitted
02 Sep 2017
Accepted
28 Nov 2017
First published
05 Dec 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 55106-55109

1,3-Dipolar [3 + 3] cycloaddition of α-halohydroxamate-based azaoxyallyl cations with hydrazonoyl chloride-derived nitrile imines

H. Zhao, Y. Zhao, Y. Liu, L. Zhao, X. Song, X. Chen, H. Pang, J. Du and N. Feng, RSC Adv., 2017, 7, 55106 DOI: 10.1039/C7RA09766B

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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