6-isotopomers have been developed, using the displace'/> Effective syntheses of 2-trimethylsilylmethyl-3-trimethylsilyl-1-propene and its 1,1-d<inf>2</inf>- and 1,1,1',1',3,3- d<inf>6</inf>-isotopomers
首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >Effective syntheses of 2-trimethylsilylmethyl-3-trimethylsilyl-1-propene and its 1,1-d2- and 1,1,1',1',3,3- d6-isotopomers
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Effective syntheses of 2-trimethylsilylmethyl-3-trimethylsilyl-1-propene and its 1,1-d2- and 1,1,1',1',3,3- d6-isotopomers

机译:有效合成2-三甲基甲硅烷基甲基-3-三甲基甲硅烷基-1-丙烯及其1,1-d 2 -和1,1,1',1',3,3-d 6 -异构体

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摘要

New and effective routes to synthesize 2-trimethylsilylmethyl-3-trimethylsilyl-1-propene and its 1,1-d2- and 1,1,1',1',3,3-d6-isotopomers have been developed, using the displacement reaction of lithium trimethylsilylcyanocuprate with allylic halides and tosylates. These compounds are pivotal precursors for the gas-phase synthesis and characterization of the trimethylenemethane anion, and for negative ion photoelectron spectroscopic investigations of the singlet-triplet splitting in trimethylenemethane. Copyright < copyright > 2001 John Wiley & Sons, Ltd.
机译:合成2-三甲基甲硅烷基甲基-3-三甲基甲硅烷基-1-丙烯及其1,1-d 2 -和1,1,1',1',3,3-d <利用三甲基甲硅烷基氰基高碳酸锂与烯丙基卤化物和甲苯磺酸盐的置换反应,开发了inf> 6 异构体。这些化合物是重要的前体,用于气相合成和表征三亚甲基甲烷阴离子,以及用于负离子的光电子能谱研究,在三亚甲基甲烷中的单重态-三重态分裂。版权<版权> 2001 John Wiley&Sons,Ltd.

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