Effective Pd-Nanoparticle (PdNP)-Catalyzed Negishi Coupling Involving Alkylzinc Reagents at Room Temperature-Reference-Cited by-同舟云学术

Effective Pd-Nanoparticle (PdNP)-Catalyzed Negishi Coupling Involving Alkylzinc Reagents at Room Temperature

Published:2008-05-29 Issue:13 Volume:10 Page:2661-2664
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Jing¹,Deng Yi¹,Wang Haibo¹,Zhang Hua¹,Yu Ganxiang¹,Wu Bingbin¹,Zhang Heng¹,Li Qiang¹,Marder Todd B.¹,Yang Zhen¹,Lei Aiwen¹

Affiliation:

1. College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, Peopleʼs Republic of China, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei 430072, Peopleʼs Republic of China, and Department of Chemistry, Durham University, South Road, Durham DH1 3LE, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol8007342

Reference58 articles.

1. Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides

2. Selective carbon-carbon bond formation via transition metal catalysts. 9. Double metal catalysis in the cross-coupling reaction and its application to the stereo- and regioselective synthesis of trisubstituted olefins

3. Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II): an effective catalyst for cross-coupling of secondary and primary alkyl Grignard and alkylzinc reagents with organic halides

4. The First Negishi Cross-Coupling Reaction of Two Alkyl Centers Utilizing a Pd−N-Heterocyclic Carbene (NHC) Catalyst

5. An Extremely Active Catalyst for the Negishi Cross-Coupling Reaction

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