Carbon−Carbon Formation via Ni-Catalyzed Suzuki−Miyaura Coupling through C−CN Bond Cleavage of Aryl Nitrile-Reference-Cited by-同舟云学术

Carbon−Carbon Formation via Ni-Catalyzed Suzuki−Miyaura Coupling through C−CN Bond Cleavage of Aryl Nitrile

Published:2009-07-13 Issue:15 Volume:11 Page:3374-3377
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yu Da-Gang¹,Yu Miao¹,Guan Bing-Tao¹,Li Bi-Jie¹,Zheng Yang¹,Wu Zhen-Hua¹,Shi Zhang-Jie¹

Affiliation:

1. Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, and State Key Laboratory of Organometallic Chemistry, SIOC, CAS, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol901217m

Reference48 articles.

1. For recent extensive reviews, see:

2. aNegishi, E.Handbook of Organopalladium Chemistry for Organic Synthesis;Negishi, E., Ed.Wiley-Interscience:New York, 2002; Vol.I, pp213−1119.

3. bMetal-Catalyzed Cross-Coupling Reactions;de Meijere, A., Diederich, F., Eds.Wiley-VCH:Weinheim, Germany, 2004; pp1−916.

4. A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides

5. Simple, Highly Active Palladium Catalysts for Ketone and Malonate Arylation: Dissecting the Importance of Chelation and Steric Hindrance

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