Nickel-catalyzed C–N bond activation: activated primary amines as alkylating reagents in reductive cross-coupling-Reference-Cited by-同舟云学术

Nickel-catalyzed C–N bond activation: activated primary amines as alkylating reagents in reductive cross-coupling

Published:2019 Issue:16 Volume:10 Page:4430-4435
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Yue Huifeng¹²³⁴^ORCID,Zhu Chen¹²³⁴^ORCID,Shen Li¹²³⁴,Geng Qiuyang¹²³⁴,Hock Katharina J.¹²³⁴^ORCID,Yuan Tingting¹²³⁴,Cavallo Luigi⁵⁶⁷⁸⁹^ORCID,Rueping Magnus¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Organic Chemistry

2. RWTH Aachen University

3. D-52074 Aachen

4. Germany

5. KAUST Catalysis Center, KCC

6. King Abdullah University of Science and Technology

7. KAUST

8. Thuwal 23955-6900

9. Saudi Arabia

Abstract

The reductive cross coupling of pyridinium salts derived from readily available primary alkyl amines with aryl halides has been achieved under mild reaction conditions using a nickel catalyst.

Funder

King Abdullah University of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC00783K

Reference41 articles.

1. T. J. Colacot , New Trends in Cross-Coupling: Theory and Applications , RSC Publishing , Cambridge , 2014

2. A. d. Meijere , S.Bräse and M.Oestreich , Metal-Catalyzed Cross-Coupling Reactions and More , Wiley-VCH , Weinheim , 2014

3. Reductive Cross-Coupling Reactions between Two Electrophiles