Nineteen 12-, 15-, 18-, 24- and 30-membered, highly unsaturatedmacrocyclic silicohydrocarbons containing -SiCCSi-, (E)-SiCHCHSi- and -SiCH2CH2Si-fragments in the ring were synthesized by the reaction of Me2Si(CCMgBr)2 or BrMgCCMe2SiCCSiMe2CCMgBr with FMe2SiCH2CH2SiMe2F; (E)-FMe2SiCHCHSiMe2F or (E, E)-(ClMe2SiCHCH)2SiMe2; (E)-BrMgCCMe2Si-CHCHSiMe2CCMgBr or Me2Si(CCSiMe2CCMgBr)2 with (E
Organosilicon compound and process for producing organosilicon compound
申请人:Agency of Industrial Science and Technology
公开号:US05151538A1
公开(公告)日:1992-09-29
An organosilicon compound having a Si--C--C--Si bond, a C.dbd.C--Si bond and/or a CH--CH--Si bond is prepared by reacting an olefin or a substituted olefin with a disilane in the presence of a platinum-containing catalyst. The resulting compound can be further treated with an alkyl lithium, an aryl lithium or a Grignard reagent.
Yarosh, O. G.; Turkina, G. Yu.; Vitkovskii, V. Yu., Journal of general chemistry of the USSR, 1989, vol. 59, # 9.2, p. 1829 - 1832
作者:Yarosh, O. G.、Turkina, G. Yu.、Vitkovskii, V. Yu.、Albanov, A. I.、Strashnikova, N. V.、Voronkov, M. G.
DOI:——
日期:——
Voronkov, M. G.; Yarosh, O. G.; Turkina, G. G. Yu., Journal of general chemistry of the USSR, 1987, vol. 57, p. 1925
作者:Voronkov, M. G.、Yarosh, O. G.、Turkina, G. G. Yu.、Vitkovskii, V. Yu.
DOI:——
日期:——
Preparation of Some Bis(fluorodimethylsilyl)alkanes
作者:Makoto Kumada、Kiyomi Naka、Yoshihiro Yamamoto
DOI:10.1246/bcsj.37.871
日期:1964.6
demethylation of bis(trimethylsilyl)alkanes of the general formula Me3SiRSiMe3 by concentrated sulfuric acid, followed by fluorination with ammonium hydrogenfluoride, can successfully be used for the method generally applicable to the preparation of bis(fluorodimethylsilyl)- alkanes, FMe2SiRSiMe2F. Although Si-Me cleavage was the main reaction in most cases, some part of the reaction gave a cleavage between
已经确定,通式 Me3SiRSiMe3 的双(三甲基甲硅烷基)烷烃用浓硫酸脱甲基,然后用氟化氢铵氟化,可以成功地用于通常适用于制备双(氟二甲基甲硅烷基)烷烃的方法, FMe2SiRSiMe2F。尽管在大多数情况下 Si-Me 裂解是主要反应,但部分反应在硅和 R 基团之间产生裂解。发现 R 从硅裂解的难易度按以下顺序降低:CH2,CHMe> (CH2)2>(CH2)3>(CH2)4,(CH2)5,(CH2)6>CHCl>CMe2