Studies in Mixed Ester Condensations. IV. Acylations with Methyl Dimethoxyacetate1
EE Royals, AG Robinson III
Index: Royals; Robinson Journal of the American Chemical Society, 1956 , vol. 78, p. 4161,4162
Full Text: HTML
Citation Number: 19
Abstract
A study has been made of the Claisen acylation of active hydrogen compounds by means of methyl dimethoxyacetate in the presence of sodium methoxide. A series of six aliphatic methyl esters was subjected to mixed ester condensation with methyl dimethoxyacetate to give the mixed condensation products in yields of 50435%. Basic cleavage of the mixed condensation products gave a-ketoacetals in yields of 73-90%. Acidic cleavage of the a- ...
Related Articles:
[Henze; Carroll Journal of the American Chemical Society, 1954 , vol. 76, p. 4580,4582]
[Henze; Carroll Journal of the American Chemical Society, 1954 , vol. 76, p. 4580,4582]
[Cuvigny,T.; Normant,H. Synthesis, 1977 , p. 198 - 200]
[Cuvigny,T.; Normant,H. Synthesis, 1977 , p. 198 - 200]
[Tiecco, M.; Testaferri, L.; Tingoli, M.; Bartoli, D. Journal of Organic Chemistry, 1990 , vol. 55, # 15 p. 4523 - 4528]