Cyclohexyne, which was generated from 2-(trimethylsilyl)cyclohexenyttriflate by fluoridepromoted ~elimination, reacts with ct-pyrones to afford the corresponding tetrahydronaphthalenes.
Polyimides by Diels-Alder polyaddition of α-pyrones
✍ Scribed by Gamil Alhakimi; Helmar Görls; Elisabeth Klemm
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 250 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
New linear polyimides 11 were synthesized via Diels‐Alder addition polymerization of α‐pyrones 9 with bismaleimides 10. The number‐average molecular weights M~n~ range from 10 000 to 34 000 g. mol (gel‐permeation chromatography). The chemical structure of these polymers is supported by X‐ray crystallography, NMR spectra and model reactions. The Diels‐Alder addition occurred with high endo selectivity.
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