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Metal-free oxysulfonylation and aminosulfonylation of alkenyl oximes: synthesis of sulfonylated isoxazolines and cyclic nitrones†
Zhong-Qi Xu,Lin-Chuang Zheng,Lin Li,Lili Duan
Organic & Biomolecular Chemistry Pub Date : 12/24/2018 00:00:00 , DOI:10.1039/C8OB02879F
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
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