| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1322709 | Journal of Organometallic Chemistry | 2010 | 4 Pages |
Abstract
C(3) functionalization of 6-alkyl-substituted-2,2â²-bipyridines was achieved through “rollover cyclopalladation” followed by carbonylation. The reaction produced novel and rare 2-(2-pyridin-2-yl)-6-alkyl-nicotinic acids or esters which contain the core of the nicotinic acid and therefore are of biological and pharmaceutical interest.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Giacomo Luigi Petretto, Antonio Zucca, Sergio Stoccoro, Maria Agostina Cinellu, Giovanni Minghetti,