Tetrahedron Letters

Reductive alkylation of 2-methoxybenzoic acid derivatives

JM Hook, LN Mander, M Woolias

Index: Hook, James M.; Mander, Lewis N.; Woolias, Michael Tetrahedron Letters, 1982 , vol. 23, # 10 p. 1095 - 1098

Full Text: HTML

Citation Number: 31

Abstract

Abstract Metal-ammonia reduction followed by in situ alkylation of 2-methoxybenzoic acids often results in substantial loss of the methoxy substituent; reduction of the carboxylate salts or esters, however, suppresses this side reaction and good to excellent yields of desired products are then obtained.

Related Articles:

The synthesis and selected chemistry of 6-alkyl-6-carbalkoxy-and 6-alkyl-6-(aminocarbonyl)-2, 4-cyclohexadien-1-ones and cyclohexadienone ketals

[Schultz, Arthur G.; Dittami, James P.; Lavieri, Frank P.; Salowey, Christina; Sundararaman, Padmanabhan; Szymula, Mary Beth Journal of Organic Chemistry, 1984 , vol. 49, # 23 p. 4429 - 4440]

More Articles...