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首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of DPPP- and DPPPEN-Type Bidentate Ligands by Ring-Opening Diphosphination of Methylene- and Vinylcyclopropanes under Visible-Light-Promoted Photoredox Catalysis
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Synthesis of DPPP- and DPPPEN-Type Bidentate Ligands by Ring-Opening Diphosphination of Methylene- and Vinylcyclopropanes under Visible-Light-Promoted Photoredox Catalysis

机译:通过在可见光促进的光致氧催化下通过亚甲基和乙烯基环丙烷的开环二膦膦合成DPPP和DPPPEN型二齿配体。

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摘要

A ring-opening diphosphination of methylene- and vinylcyclopropanes with tetraaryldiphosphines (Ar2P-PAr2) has been developed to afford the corresponding 1,3-diphenylphosphinopropane- and 1,3-diphenylphosphinopentane-type bidentate ligands, respectively. The reaction proceeds under bromine cation-initiated, visible-light-promoted photoredox catalysis at ambient temperature. Owing to the ready availability of functionalized diphosphines, the electronically diverse MeO- and CF3-substituted bidentate ligands are also easily prepared.
机译:已经开发出具有四芳基二膦酰基(AR2P-PAR2)的亚甲基和乙烯基环丙烷的开环二磷酸化,得到相应的1,3-二苯基膦丙烷和1,3-二苯基膦酰戊烷型二齿配体。 反应在环境温度下在溴阳离子引发的可见光促进的光毒剂催化下进行。 由于官能化二膦的随的可用性,也可以容易地制备电子各种MeO-和CF3取代的二齿配体。

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