A Practical Route for the Preparation of Substituted 6-oxo-2-Hexenoate Derivatives.
โ Scribed by Marta Freiria; Andrew J. Whitehead; William B. Motherwell
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 117 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Oxocarboxylic acids and esters
Oxocarboxylic acids and esters P 0290
A Practical Route for the Preparation of Substituted 6-oxo-2-Hexenoate Derivatives.
-The reaction of 2-hydroxy-3-butenoates [cf. (I)] with the aldehydes (II) generates alkyl allyl ethers which undergo Claisen rearrangement to give 6-substituted 6-oxo-2-hexenoates (III). Acetaldehyde diethyl acetal (IV) and benzylideneacetone (VI) react similarly under these conditions. -(
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The synthesis and characterization of poly(4-hydroxystyrene) (PHS) and poly(4-vinylphenol) (PVPh) by the polymer modification route are reported. Polystyrene prepared by free-radical and anionic polymerization was acetylated quantitatively to poly(4-acetylstyrene) (ACPS) with acetyl chloride and anh