Mechanism of decarbalkoxylation of arylmethylene-propanedioic acid dimethyl esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Synthetic Applications of Dealkoxycarbonylations of Malonate Esters, β-Keto Esters, α-Cyano Esters and Related Compounds in Dipolar Aprotic Media - Part I
2. Stereochemistry of decarbalkoxylation of cyclic geminal diesters effected by water and lithium chloride in dimethyl sulfoxide
3. Stereochemistry of the dealkoxycarbonylation of methyl α-cyanocinnamate and of the decarboxylation of the corresponding cyanoacid: a facile stereoselective route to Z-cinnamonitrile
4. Stereochemistry of decarbalkoxylation of arylmethylene-propanedioic acids dimethyl esters
5. Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts
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5. Ionic liquids via reaction of the zwitterionic 1,3-dimethylimidazolium-2-carboxylate with protic acids. Overcoming synthetic limitations and establishing new halide free protocols for the formation of ILs;Green Chem.;2007
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