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首页> 外文期刊>European journal of inorganic chemistry >Synthesis of BINAM-Based Chiral Di-1,2,3-triazolylidene Complexes and Application of the Di-NHC Rh-I Catalyst in Enantioselective Hydrosilylation
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Synthesis of BINAM-Based Chiral Di-1,2,3-triazolylidene Complexes and Application of the Di-NHC Rh-I Catalyst in Enantioselective Hydrosilylation

机译:BINAM基手性二1,2,3-三唑基亚甲基配合物的合成及Di-NHC Rh-1催化剂在对映选择性硅氢加成反应中的应用

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摘要

Despite the prolific use of (di-)NHC complexes in homogeneous catalysis, there are relatively few reports on their successful application in asymmetric transformations. In this work the atropisomeric binaphthyl backbone was combined with readily obtainable 1,2,3-triazolylidenes to develop a strongly electron-donating C-2-symmetric ligand. The ligand was efficiently synthesized in a three-step procedure in an overall yield of 91% starting from commercially available materials. Strategies for the synthesis of the corresponding di-NHC silver(I), palladium(II), rhodium(I), and iridium(I) complexes have been developed. The rhodium(I) complex was employed in the catalytic asymmetric hydrosilylation of ketones, providing good conversions at catalyst loadings as low as 0.2 mol-% and giving chiral inductions of up to 51% ee.
机译:尽管在均相催化中大量使用了(di-)NHC配合物,但有关将其成功用于不对称转化的报道相对较少。在这项工作中,将阻转异构的双萘基骨架与易于获得的1,2,3-三唑基亚烷基结合,形成了强供电子的C-2-对称配体。从市售材料开始,以三步法有效地合成了配体,总产率为91%。已经开发了合成相应的二-NHC银(I),钯(II),铑(I)和铱(I)配合物的策略。铑(I)配合物用于酮的催化不对称硅氢加成反应,在低至0.2 mol%的催化剂负载量下提供良好的转化率,手性诱导率高达ee的51%。

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