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求20篇以上关于荧光探针开发与研究进程的外文文献

ieehcgh 2018-12-07 01:01:31 346  浏览
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文献求翻译
Since the formation of a titanacyclopropane en route to cyclopropylamines can only occur with alkylmagnesium halides that contain a b-hydrogen atom, Grignard reagents without b-hydrogens appeared to be the most promising reagents for th... Since the formation of a titanacyclopropane en route to cyclopropylamines can only occur with alkylmagnesium halides that contain a b-hydrogen atom, Grignard reagents without b-hydrogens appeared to be the most promising reagents for the synthesis of primary tert-alkylamines from nitriles (Scheme 1). Thus propionitrile (1a), phenylmagnesium bromide (2) and Ti(Oi-Pr)4 were chosen to optimize the reaction conditions. In the protocol for the synthesis of cyclopropylamines,10 Ti(Oi-Pr)4 is already present in the diethyl ether solution of a nitrile, before two equivalents of the Grignard reagent are added. As this did not appear to be optimal for the synthesis of primary tertalkylamines, the Grignard reagent was added before Ti(Oi-Pr)4. With 2 equivalents of PhMgBr, 0.1 equivalent of Ti(Oi-Pr)4, and 1 equivalent of propionitrile (1a), the primary tert-alkylamine 8a was not formed at all. With an equimolar quantity of Ti(Oi-Pr)4, the amine 8a was produced in a low yield (11%) but with 1 equivalent of Ti(Oi- Pr)4 and 3 equivalents of the Grignard reagent 2, a 60% yield of 8a was obtained. Monitoring of the reaction by workup of aliquots of the reaction mixture showed that the first addition of 2 to form the N-magnesio derivative of the corresponding imine was rapid, whereas the subsequent second addition of the Grignard reagent 2 required heating under reflux for up to 24 hours. In tetrahydrofuran instead of diethyl ether, the amine 8a was formed in a very low yield, if at all. 展开
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