Base-mediated tandem sulfonylation and oximation of alkenes in water-Reference-Cited by-同舟云学术

Base-mediated tandem sulfonylation and oximation of alkenes in water

Published:2017 Issue:24 Volume:19 Page:5794-5799
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Wang Bin¹²³⁴⁵,Tang Lin¹²³⁴⁵,Liu Liyan¹²³⁴⁵,Li Yanan¹²³⁴⁵,Yang Yu¹²³⁴⁵,Wang Zhiyong¹²³⁴⁵^ORCID

Affiliation:

1. Hefei National Laboratory for Physical Sciences at Microscale

2. CAS Key Laboratory of Soft Matter Chemistry and Department of Chemistry & Collaborative Innovation Center of Suzhou Nano Science and Technology

3. University of Science and Technology of China

4. Hefei

5. P. R. China

Abstract

A base-mediated bifunctionalization of alkenes for the synthesis of α-sulfonylethanone oximes was developed in water under metal-free conditions. This reaction features a wide substrate scope and facile starting materials to afford the desired products in high yields.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/GC/C7GC03051G

Reference114 articles.

1. Recent advances in transition-metal-free carbon–carbon and carbon–heteroatom bond-forming reactions using arynes

2. Transition-metal-free B–B and B–interelement reactions with organic molecules

3. Transition-metal-free C–C bond forming reactions of aryl, alkenyl and alkynylboronic acids and their derivatives