Issue 42, 2016

Enolate-mediated 1,3-dipolar cycloaddition reactions of allyl ketones with nitrile oxides: direct access to 3,5-disubstituted isoxazolines

Abstract

TMG-promoted [3 + 2] organocatalytic 1,3-dipolar cycloaddition reactions of allyl ketones with in situ generated nitrile oxides have been developed. This strategy could generate 3,5-disubstituted isoxazolines in high yields and regioselectivities.

Graphical abstract: Enolate-mediated 1,3-dipolar cycloaddition reactions of allyl ketones with nitrile oxides: direct access to 3,5-disubstituted isoxazolines

Supplementary files

Article information

Article type
Communication
Submitted
15 Sep 2016
Accepted
05 Oct 2016
First published
05 Oct 2016

Org. Biomol. Chem., 2016,14, 9985-9988

Enolate-mediated 1,3-dipolar cycloaddition reactions of allyl ketones with nitrile oxides: direct access to 3,5-disubstituted isoxazolines

W. Li, X. Zhou, Z. Shi, Y. Liu, Z. Liu and H. Gao, Org. Biomol. Chem., 2016, 14, 9985 DOI: 10.1039/C6OB02025A

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