Journal of the American Chemical Society

Mechanism of the Reaction between Hindered Carbonyl Compounds and the Grignard Reagent. II1

RT Arnold, RW Liggett

Index: Arnold; Liggett Journal of the American Chemical Society, 1942 , vol. 64, p. 2875

Full Text: HTML

Citation Number: 13

Abstract

\ O-R'abnormally by the Grignard reagent if in R-there are substituents which sterically hinder additions to the carbonyl group of the ester, and if R'-is of such a nature that it has considerable thermodynamic stability as a cation (R'+). The general reaction between such an ester and the Grignard reagent can be expressed by the equation

Related Articles:

The synthesis of all of the dimethyldibenzothiophenes and monoethyldibenzothiophenes

[Tedjamulia, Marvin L.; Tominaga, Yoshinori; Castle, Raymond N. Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 1485 - 1495]

Photoinduced Electron Transfer Promoted Radical Ring Expansion and Cyclization Reactions of α-(ω-Carboxyalkyl) β-Keto Esters

[Nishikawa, Keisuke; Ando, Tomoki; Maeda, Kousuke; Morita, Toshio; Yoshimi, Yasuharu Organic Letters, 2013 , vol. 15, # 3 p. 636 - 638]

More Articles...