Reductive insertion of sulfur dioxide for the synthesis of trifluoromethyl thiolsulphonates through a one-pot reaction of aniline and trifluoromethanesulfanylamide-Reference-Cited by-同舟云学术

Reductive insertion of sulfur dioxide for the synthesis of trifluoromethyl thiolsulphonates through a one-pot reaction of aniline and trifluoromethanesulfanylamide

Published:2017 Issue:1 Volume:4 Page:95-100
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Sheng Jie¹²³⁴,Li Yuewen⁵⁶⁷⁸⁴,Qiu Guanyinsheng⁵⁶⁷⁸⁴

Affiliation:

1. College of Food Science and Technology

2. Shanghai Ocean University

3. Shanghai

4. China

5. College of Biological

6. Chemical Science and Engineering

7. Jiaxing University

8. Jiaxing 314001

Abstract

A bismuth(iii) chloride-mediated three-component reaction of anilines, sulfur dioxide, and trifluoromethanesulfanylamide is reported herein for the efficient synthesis of antifungal trifluoromethyl thiolsulphonates with a good reaction scope.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00530F

Reference58 articles.

1. Fixation of sulfur dioxide into small molecules

2. One-pot three-component sulfone synthesis exploiting palladium-catalysed aryl halide aminosulfonylation