Oxidative Addition of Aryl Halides to Transient Anionic à-Aryl–Palladium(0) Intermediates—Application to Palladium-Catalyzed Reductive Coupling of Aryl Halides-Reference-Cited by-同舟云学术

Oxidative Addition of Aryl Halides to Transient Anionic à-Aryl–Palladium(0) Intermediates—Application to Palladium-Catalyzed Reductive Coupling of Aryl Halides

Published:1996-08 Issue:8 Volume:2 Page:957-966
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:de
Short-container-title:Chem. Eur. J.

Author:

Amatore Christian,Carré Emmanuelle,Jutand Anny,Tanaka Hideo,Ren Qinghua,Torii Sigeru

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference51 articles.

1. For earliest works see: a) , Bull. Soc. Chim. Fr. 1976, 765.

2. The cross-coupling of aryl halides with grignard reagents catalyzed by iodo(phenyl)bis(triphenylphosphine)palladium(II)

3. Palladium-catalyzed reactions of organic halides with olefins

4. Nickel and palladium complex catalyzed cross-coupling reactions of organometallic reagents with organic halides

5. Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation

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