NC palladacycles in the Heck arylation of ethylene: synthesis, structure and their reactivity
Title | NC palladacycles in the Heck arylation of ethylene: synthesis, structure and their reactivity |
Publication Type | Journal Article |
Year of Publication | 2009 |
Authors | Atla, SB, Kelkar, AA, Puranik, VG, Bensch, W, Chaudhari, RV |
Journal | Journal of Organometallic Chemistry |
Volume | 694 |
Issue | 5 |
Pagination | 683-690 |
Date Published | MAR |
ISSN | 0022-328X |
Keywords | alpha-Aryl propionic acids, Arylation, Palladacycle |
Abstract | Monomeric cyclopalladated complexes with NC coordination using ligands 2-phenylpyridine, 2-phenylquinoline, 8-methylquinoline have been synthesized and the structures have been determined by single crystal X-ray structure analysis. The crystal structures of monomeric palladacycles prepared using benzophenone oxime, and 2-phenylpyridine have also been determined. The use of these complexes in the Heck arylation of ethylene with 2-bromo-6-methoxynaphthalne (BMN) to give 2-vinyl-6-methoxynapthalene which is an intermediate for the synthesis of anti-inflammatory drug Naproxen has been examined and also arylation of ethylene with 3-bromo-benzophenone and 4-bromo-isobutylbenzene was investigated. These palladacycles with NC coordination show excellent catalytic activity with a TOF > 4000 h (1). (C) 2008 Elsevier B.V. All rights reserved. |
DOI | 10.1016/j.jorganchem.2008.11.065 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.205 |