首页> 外文期刊>Organic Syntheses >Discussion Addendum for: dl-Selective Pinacol-Type Coupling Using Zinc, Chlorosilane, and Catalytic Amounts of Cp2VCl2; dl-1,2- Dicyclohexylethanediol (1,2-Ethanedidl,1,2-dicyclohexyl-)
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Discussion Addendum for: dl-Selective Pinacol-Type Coupling Using Zinc, Chlorosilane, and Catalytic Amounts of Cp2VCl2; dl-1,2- Dicyclohexylethanediol (1,2-Ethanedidl,1,2-dicyclohexyl-)

机译:讨论附录:使用锌,氯硅烷和催化量的Cp2VCl2的dl选择性Pinacol型偶联; dl-1,2-二环己基乙二醇(1,2-乙二胺基,1,2-二环己基-)

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摘要

The pinacol coupling reaction achieves reductive carbon-carbon bond formation from carbonyl compounds by low-valent early transition metals to give 1,2-diols. A catalytic system for the pinacol coupling was developed for the first time in our group. Catalytic, diastereoselective, and/or enantioselective methods have been reported recently. Organic reaction in water or aqueous media is of interest in organic synthesis from the vantage points of its cost, safety, and environmental concern. Therefore, the development of an efficient synthetic methodology to form a carbon-carbon bond in water or aqueous media appears to be of importance. Here, a vanadium-catalyzed pinacol coupling reaction in water is described.
机译:频哪醇偶联反应通过低价的早期过渡金属从羰基化合物形成还原性碳-碳键,从而生成1,2-二醇。频哪醇偶联的催化系统是我们小组中的第一次开发。最近已经报道了催化,非对映选择性和/或对映选择性方法。从其成本,安全性和环境关注的角度出发,水或水性介质中的有机反应是有机合成中的关注点。因此,开发在水或水性介质中形成碳-碳键的有效合成方法似乎很重要。这里,描述了在水中钒催化的频哪醇偶联反应。

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