The Journal of Organic Chemistry

Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl (aryl) pyridines

DL Comins, AH Abdullah

Index: Comins, Daniel L.; Abdullah, Abdul H. Journal of Organic Chemistry, 1982 , vol. 47, # 22 p. 4315 - 4319

Full Text: HTML

Citation Number: 186

Abstract

Our results show that due to a lack of regioselectivity the reacton of Grignard reagents with 1- acylpyridinium chlorides is limited in scope with regard to the synthesis of 2-alkylpyridines. However, the method may be valuable for the preparation of 2-arylpyridines since aryl Grignard reagents appear to have a greater preference for attack at the 2-position than their aliphatic counterparts. The method is useful for the preparation of 2-substituted 4- ...

Related Articles:

A series of non-quinoline cysLT 1 receptor antagonists: Sar study on pyridyl analogs of singulair®

[Guay, Daniel; Gauthier; Dufresne; Jones; McAuliffe; McFarlane; Metters; Prasit; Rochette; Roy; Sawyer; Zamboni Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 5 p. 453 - 458]

More Articles...