Synthesis of substituted polymethylenes from alkyl cinnamates bearing bulky alkyl ester groups
β Scribed by Akikazu Matsumoto; Atsushi Horie; Takayuki Otsu
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 372 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Radical and anionic polymerizations of alkyl cinnamates (RCi) bearing bulky alkyl groups, such as isopropyl or t-butyl, were performed. Radical homopolymerization of RCi hardly occurred even in bulk at high temperature, whereas copolymerization with dialkyl fumarates, as another 1,2-disubstituted ethylene, gave a high molecular weight substituted copolymethylene. It has been shown that RCi polymerizes with s-butyllithium as an anionic initiator in tetrahydrofuran or toluene. The structures and thermal properties of the resulting polymethylenes were examined.
π SIMILAR VOLUMES
8-Alkyl-substituted carboxylates were synthesized in good yields from U,B-unsaturated aldehydes by using the 1:l carbonyl adducts with diethyl bis(trimethylsily1) phosphite. Recently, several studies on acyl anion equivalents utilizing carbonyl insertion reactions have appeared. 2 It has been report
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