Issue 4, 2019

Metal-free oxysulfonylation and aminosulfonylation of alkenyl oximes: synthesis of sulfonylated isoxazolines and cyclic nitrones

Abstract

Intramolecular oxysulfonylation of alkenyl oximes was reported. Using iodine as the catalyst, TBHP as the oxidant, and sulfonyl hydrazides as the sulfonyl radical source, a variety of sulfonylated isoxazolines were obtained in moderate to excellent yields. Cyclic nitrones could also be readily obtained under the same conditions.

Graphical abstract: Metal-free oxysulfonylation and aminosulfonylation of alkenyl oximes: synthesis of sulfonylated isoxazolines and cyclic nitrones

Supplementary files

Article information

Article type
Paper
Submitted
18 Nov 2018
Accepted
21 Dec 2018
First published
24 Dec 2018

Org. Biomol. Chem., 2019,17, 898-907

Metal-free oxysulfonylation and aminosulfonylation of alkenyl oximes: synthesis of sulfonylated isoxazolines and cyclic nitrones

Z. Xu, L. Zheng, L. Li, L. Duan and Y. Li, Org. Biomol. Chem., 2019, 17, 898 DOI: 10.1039/C8OB02879F

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