2009
DOI: 10.1016/j.jorganchem.2009.01.030
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1,4-bis[2,2-bis(trimethylsilyl)ethenyl]benzene: Regioselective ring opening of its α,β-epoxybis(silane) with some nucleophiles

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Cited by 24 publications
(17 citation statements)
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“…As a part of our continuing research on the organosilicon chemistry [19][20][21][22][23][24], we have particularly been interested in developing the alcoholysis reaction between PMHS and various simple and functional alcohols. The objective of this research is the preparation of novel and functional poly(methylalkoxysiloxane) in mild conditions and high yield approach in the presence of Speier's and Karstedt's catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…As a part of our continuing research on the organosilicon chemistry [19][20][21][22][23][24], we have particularly been interested in developing the alcoholysis reaction between PMHS and various simple and functional alcohols. The objective of this research is the preparation of novel and functional poly(methylalkoxysiloxane) in mild conditions and high yield approach in the presence of Speier's and Karstedt's catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…The resulting product (1) shows that the migration of sulphur to carbon of C(SiMe 3 ) 2 has been occurred. It seems likely that the obtained product (1) forms through the intermediates 1de1g and after hydrolysis of 1g (Scheme 2).…”
Section: Resultsmentioning
confidence: 99%
“…Cu/SAPO-34 We have recently used bulky tris(trimethylsilyl)-methyllithium (TsiLi) as a reagent for the preparation of vinylsilanes, epoxysilanes, halovinylsilanes, silyl ethers, etc. [25][26][27][28][29][30]. In the previous publication, we reported the synthesis of bulky organosilicon groups containing highly substituted imidazoles using silyl-substituted organometallic reagents (RSiMe 2 ) 3 CLi (R = H, Me, Ph) [31,36].…”
Section: Resultsmentioning
confidence: 99%