Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides-Reference-Cited by-同舟云学术

Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides

Published:2006-04 Issue:14 Volume:47 Page:2427-2430
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tang Zhen-Yu,Spinella Stephen,Hu Qiao-Sheng

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids

2. Synthesis of Optically Pure Clausenamine-A and its Demethoxylated Analogs

3. Aryl Mesylates in Metal-Catalyzed Homocoupling and Cross-Coupling Reactions. 1. Functional Symmetrical Biaryls from Phenols via Nickel-Catalyzed Homocoupling of Their Mesylates

4. Organoboron Compounds

5. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998

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