A Convenient Method for the Preparation of Methyl trans-4-Oxo-2-alkenoates

OG Kulinkovich, IG Tischenko, JN Romashin…

Index: Kulinkovich, O. G.; Tischenko, I. G.; Romashin, J. N.; Savitskaya, L. N. Synthesis, 1986 , # 5 p. 378 - 379

Full Text: HTML

Citation Number: 5

Abstract

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular ...

Related Articles:

Studies on structurally simple α, β-butenolides—I: New syntheses of racemic γ-hydroxymethyl-α, β-butenolide and derivatives

[Cardellach, J.; Estopa, C.; Font, J.; Moreno-Manas, M.; Ortuno, R. M.; et al. Tetrahedron, 1982 , vol. 38, # 15 p. 2377 - 2394]

The synthesis of 4-oxo-2-pentenoic esters by Wittig reaction using α-oxoesters

[Schuda, Paul Francis; Ebner, Cynthia B.; Potlock, Steven J. Synthesis, 1987 , # 12 p. 1055 - 1057]

An efficient and highly flexible synthesis of (α), β-unsaturated γ-oxoesters

[Boehm, Ingrid; Schulz, Rick; Reissig, Hans-Ulrich Tetrahedron Letters, 1982 , vol. 23, # 19 p. 2013 - 2016]

Favorskii-type rearrangement of chlorinated acetylacetone monomethyl enol ethers. Presumptive evidence for a cyclopropane dimethyl acetal intermediate

[Verhe,R. et al. Journal of Organic Chemistry, 1977 , vol. 42, # 7 p. 1256 - 1258]

Favorskii-type rearrangement of chlorinated acetylacetone monomethyl enol ethers. Presumptive evidence for a cyclopropane dimethyl acetal intermediate

[Verhe,R. et al. Journal of Organic Chemistry, 1977 , vol. 42, # 7 p. 1256 - 1258]

More Articles...