Synthesis of surface organopalladium intermediates in coupling reactions: the mechanistic insight

Choudary, Boyapati M. ; Madhi, Sateesh ; Kantam, Mannepalli L. ; Sreedhar, Bojja ; Iwasawa, Yasuhiro (2004) Synthesis of surface organopalladium intermediates in coupling reactions: the mechanistic insight Journal of the American Chemical Society, 126 (8). pp. 2292-2293. ISSN 0002-7863

Full text not available from this repository.

Official URL: http://pubs.acs.org/doi/abs/10.1021/ja038270f

Related URL: http://dx.doi.org/10.1021/ja038270f

Abstract

The design and synthesis of surface transient organometallic intermediates on nanopalladium supported on layered double hydroxides is conceived and developed for the first time. The formation of only one STO intermediate in all the Heck-, Suzuki-, Sonogashira-, and Stille-type coupling reactions during their reaction sequences and the excellent isolated yields of each of the coupling products from the corresponding organometallic complexes not only validate the mechanism but also demonstrate the evolution of the single-site heterogeneous catalyst.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:6664
Deposited On:22 Oct 2010 05:26
Last Modified:28 May 2011 08:57

Repository Staff Only: item control page