Novel polyesters containing sulphide, sulphone and carbonyl groups are reported. Three diacids were prepared through several steps from 1,4-bis(p-phenylthio)benzene, bis(p-phenylthio)-diphenyl sulphone and bis(p-phenylthio)-benzophenone. Three model diesters (MDE-I,2,3) were prepared. The model comp
Synthesis of vinyl polymers containing α-substituted γ-butyrolactone groups in their backbones
✍ Scribed by Zutty, N. L. ;Welch, F. J.
- Book ID
- 104532470
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1963
- Tongue
- English
- Weight
- 566 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0449-2951
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✦ Synopsis
Abstract
When vinyl chloride—methyl methacrylate copolymers having a uniform chain‐to‐chain composition, are pyrolyzed at temperatures around 150°C., an intramolecular lactonization occurs forming α‐methyl‐γ‐butyrolactone groups in the polymer backbone concomitant with the quantitative elimination of methyl chloride. This reaction has been shown to be a general reaction for copolymers containing α‐substituted γ‐haloester groups in their backbone. The formation of the lactone groups in these polymers leads to increased chain rigidity and higher polymer softening points. Advantage has been taken of the gaseous alkyl halide elimination to produce rigid vinyl foams of good compressive strengths.
📜 SIMILAR VOLUMES
Substituted trans-a, /3-dibenzyl-y-butyrolactones were synthesized in a diastereoselective manner by the reaction of the potassium enolates of a, &dibenzyl-ybutyrolactones with electrophiles. The method was applied to the synthesis of (k)trachelogenin.
Palladium-Catalysed Vinylic Substitution of Aryl
Using several easily accessed and inexpensive chiral auxiliaries derived from carbohydrates, all four stereoisomers of the optically active a,g-substituted g-butyrolactones were obtained respectively in high enantiomeric purities (up to 96% ee for trans and up to >99% ee for cis) by the SmI 2 -induc