Effective, transition metal free and selective C–F activation under mild conditions-Reference-Cited by-同舟云学术

Effective, transition metal free and selective C–F activation under mild conditions

Published:2015 Issue:10 Volume:5 Page:7035-7048
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Kong Xianqiang¹²³⁴,Zhang Huizi¹²³⁴,Xiao Yunqing¹²³⁴,Cao Changsheng¹²³⁴,Shi Yanhui¹²³⁴,Pang Guangsheng⁵⁶⁷⁸⁴

Affiliation:

1. School of Chemistry and Chemical Engineering and Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials

2. Jiangsu Normal University

3. Xuzhou

4. P. R. China

5. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry

6. College of Chemistry

7. Jilin University

8. Changchun

Abstract

A simple and effective aromatic nucleophilic monosubstitution reaction for the synthesis of aromatic amines via selective C–F bond cleavage of various fluoroarenes with primary and secondary aromatic amines is demonstrated.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C4RA13753A

Reference74 articles.

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3. T. Hiyama , K.Kanie, T.Kusumoto, Y.Morizawa and M.Shimizu, in Organofluorine Compounds: Chemistry and Application, Springer-Verlag, Berlin, 2000

4. J.-P. Bégué and D.Bonnet-Delpon, in Bioorganic and Medicinal Chemistry of Fluorine, John Wiley & Sons, Inc., Hoboken, NJ, 2008

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