Preparation of Ketones from α, α-Disubstituted Acetoacetic Esters

WB Renfrow, GB Walker

Index: Renfrow; Walker Journal of the American Chemical Society, 1948 , vol. 70, p. 3957

Full Text: HTML

Citation Number: 15

Abstract

The ketonic cleavage is favored by a low concentration of alkali,'but maximum yields of ketones vary widely with the nature of the groups R and R'. Esters in which both R and R'are methyl, ethyl or n-butyl groups give 60-84% yieldszJ of ketones, but we have found that when R was an n-butyl group and R'was either an i-butyl or s-butyl group the yields of ketones were very low (lOo/o) and yields of disubstituted acetates were high even when ...

Related Articles:

Synthesis of 7-epineoptilocaulin, mirabilin B, and isoptilocaulin. A unified biosynthetic proposal for the ptilocaulin and batzelladine alkaloids. Synthesis and structure …

[Snider,B.B.; Faith,W.C. Journal of the American Chemical Society, 1984 , vol. 106, p. 1443 Full Text View citing articles Show Details Snider; Faith Tetrahedron Letters, 1983 , vol. 24, # 9 p. 861 - 864]

More Articles...