Aerobic Copper-Promoted Radical-Type Cleavage of Coordinated Cyanide Anion: Nitrogen Transfer to Aldehydes To Form Nitriles-Reference-Cited by-同舟云学术

Aerobic Copper-Promoted Radical-Type Cleavage of Coordinated Cyanide Anion: Nitrogen Transfer to Aldehydes To Form Nitriles

Published:2016-02-29 Issue:9 Volume:138 Page:2885-2888
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wu Qian¹,Luo Yi²,Lei Aiwen²,You Jingsong¹

Affiliation:

1. Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, and State Key Laboratory of Biotherapy, West China Medical School, Sichuan University, 29 Wangjiang Road, Chengdu 610064, P. R. China

2. College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b10945

Reference64 articles.

1. Factors influencing the reductive cleavage of C-X multiple bonds in their reactions with metal-metal multiple bonds (X = C, N, O, S)

2. Additions to Metal-Activated Organonitriles

3. Alkyne metathesis

4. Research inspired by the chemistry of nitrogenase Novel metal complexes and their reactivity toward dinitrogen, nitriles, and alkynes

5. Ring closing enyne metathesis: A powerful tool for the synthesis of heterocycles

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