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首页> 外文期刊>Russian Journal of General Chemistry >1-(TrifluoromethylsuIfonyl)-4,4-dimethyl-4-silapiperidine
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1-(TrifluoromethylsuIfonyl)-4,4-dimethyl-4-silapiperidine

机译:1-(三氟甲基磺酰基)-4,4-二甲基-4-硅哌啶

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摘要

After the synthesis of the first representatives of 4-silapiperidines (1,4-azasilinanes) in 1982 [1, 2], only a few works appeared in the literature [3-9] concerning these compounds showing biological activity [5-9], which were summarized in the recent review [10]. At the same time, 1,4-azasilinanes can be considered as N-protected primary amines, in which the organosilicon protecting group can be removed by treatment with alkali fluorides [3]. They also are interesting objects for structural investigations since for a series of N-trifluoromethylsulfonyl-substituted six-membered N-heterocycles an interesting stereo-dynamic behavior was found ([11, 12] and references -therein). N-Sulfonyl-substituted 4-silapiperidines R2Si(CH2CH2)2NSO2R' are not described in the literature. In the present work, we have synthesized their first representative, 1-trifluoro-methylsulfonyl-4,4-dimethyl-4-silapiperidine (II).
机译:在1982年合成了4-silapiperidines(1,4-azasilinanes)的首批代表[1,2]之后,关于这些化合物具有生物学活性的文献[3-9]仅出现了少量著作[5-9]。 ,最近的综述中对此进行了总结[10]。同时,可以将1,4-氮杂亚麻烷视为N保护的伯胺,其中有机硅保护基可以通过用碱金属氟化物处理而除去[3]。它们也是结构研究的有趣对象,因为对于一系列N-三氟甲基磺酰基取代的六元N-杂环,发现了有趣的立体动力学行为([11,12]和参考文献-thein)。在文献中没有描述N-磺酰基取代的4-硅哌啶R 2 Si(CH 2 CH 2)2 NSO 2 R'。在目前的工作中,我们合成了它们的第一个代表性的化合物,即1-三氟甲基磺酰基-4,4-二甲基-4-硅哌啶(II)。

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