Preparation and reactions of some organosilicon cyanates
β Scribed by Colin Eaborn; Yousef Y. El-Kaddar; Paul D. Lickiss
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 974 KB
- Volume
- 198-200
- Category
- Article
- ISSN
- 0020-1693
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β¦ Synopsis
from traces of water). Reaction of 1 with KSCN in MeCN gives exclusively the substitution product TsiSiMe,NCS, but CsF and NaN,, which are only very slightly soluble, promote very predominant isomerization. Possible mechanisms of the isomerizations are discussed. Cyanate is a markedly better leaving group from silicon than iodide, and comparable with triflate.
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A review of advances in the applications of the Diels-Alder reaction in organosilicon chemistry in our laboratory is presented. Using this reaction, we have synthesized a series of organosilicon monomers and polymers with polyphenyl groups and condensed rings and established a novel vulcanization sy