Catalytic enantioselective synthesis of fluoromethylated stereocenters by asymmetric hydrogenation-Reference-Cited by-同舟云学术

Catalytic enantioselective synthesis of fluoromethylated stereocenters by asymmetric hydrogenation

Author:

Yang Jianping¹,Ponra Sudipta¹,Li Xingzhen²,Peters Bram B. C.¹^ORCID,Massaro Luca¹^ORCID,Zhou Taigang²^ORCID,Andersson Pher G.¹³^ORCID

Affiliation:

1. Department of Organic Chemistry, Stockholm University, Arrhenius Laboratory, 106 91, Stockholm, Sweden

2. College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, Sichuan 610500, China

3. School of Chemistry and Physics, University of Kwazulu-Natal, Private Bag X54001, Durban, 4000, South Africa

Abstract

Herein, a catalytic asymmetric hydrogenation to synthesize various products bearing fluoromethylated stereocenters has been developed.

Funder

National Natural Science Foundation of China

Knut och Alice Wallenbergs Stiftelse

Stiftelsen Olle Engkvist Byggmästare

Swedish Foundation for International Cooperation in Research and Higher Education

Vetenskapsrådet

Sichuan Province Science and Technology Support Program

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

Reference89 articles.

3. K.Uneyama , Organofluorine Chemistry , John Wiley & Sons , 2008

5. P. V.Reddy , Organofluorine Compounds in Biology and Medicine , Newnes , 2015

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