首页> 美国政府科技报告 >Epoxidation of E-1,4-poly(2-triethylsilyl-1,3-butadiene) and E-1,4-poly-(2,3-bis(trimethylsilyl)-1,3-butadiene). Stereochemical analysis of E-1,4-poly(2,3-epoxy-2-triethylsilyl-1,3-butadiene) and E-1,4-poly-(2,3-bis(trimethylsilyl
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Epoxidation of E-1,4-poly(2-triethylsilyl-1,3-butadiene) and E-1,4-poly-(2,3-bis(trimethylsilyl)-1,3-butadiene). Stereochemical analysis of E-1,4-poly(2,3-epoxy-2-triethylsilyl-1,3-butadiene) and E-1,4-poly-(2,3-bis(trimethylsilyl

机译:E-1,4-聚(2-三乙基甲硅烷基-1,3-丁二烯)和E-1,4-聚 - (2,3-双(三甲基甲硅烷基)-1,3-丁二烯)的环氧化。 E-1,4-聚(2,3-环氧-2-甲基甲硅烷基-1,3-丁二烯)和E-1,4-聚 - (2,3-双(三甲基甲硅烷基)的立体化学分析

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摘要

There is considerable interest in chemical modification of intact polymers. In this regard, stereoselective cis-epoxidation of polybutadiene and polyisoprene with peracids have been reported . While the reaction of monomeric vinylsilanes with peracids to yield alpha, beta-epoxysilanes has been studied similar reactions on polymeric vinyl silane systems are unexplored. Monomeric alpha, beta-epoxysilanes are of synthetic interest since, for example, they can be converted into carbonyl groups by acidic hydrolysis. This transformation is regiospecific in that the silyl substituted carbon is converted to the carbonyl carbon. Reprints. (MJM)

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