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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Manganese(III) complexes of novel chiral unsymmetrical BINOL-Salen ligands: Synthesis, characterization, and application in asymmetric epoxidation of olefins
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Manganese(III) complexes of novel chiral unsymmetrical BINOL-Salen ligands: Synthesis, characterization, and application in asymmetric epoxidation of olefins

机译:新型手性不对称BINOL-Salen配体的锰(III)配合物:烯烃的合成,表征及在不对称环氧化中的应用

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摘要

Several chiral unsymmetrical and C2-symmetric Mn(III)-BINOL-Salen complexes have been designed, synthesized and applied to the asymmetric epoxidation of non-functionalized alkenes. Experimental results show these complexes are effective in the catalytic asymmetric epoxidation of alkenes. The catalyst 4c exhibited better enantioselectivity and reactivity than the catalysts 4b and 4a due to the steric effect of the ligands. To understand the synergistic effect of the two different chiral centers in the catalyst, the catalyst 6a has been investigated. By comparison of the enantioselectivity obtained by using 4c and 6a, respectively, the positive experimental results have proved that the chiral stereogenic centers in the diaminocyclohexane-derived catalysts played an important role in the current enantioselective epoxidation. Besides, the comparison of enantioselectivity displayed by 4c and 7a further demonstrates the significant influence through the cooperation of steric factors and chiral centers in catalyst.
机译:几种手性不对称和C2对称的Mn(III)-BINOL-Salen配合物已被设计,合成并应用于非官能化烯烃的不对称环氧化。实验结果表明,这些配合物可有效地催化烯烃的不对称环氧化。由于配体的空间效应,催化剂4c表现出比催化剂4b和4a更好的对映选择性和反应性。为了理解催化剂中两个不同手性中心的协同作用,已经研究了催化剂6a。通过比较分别使用4c和6a获得的对映选择性,积极的实验结果证明,二氨基环己烷衍生的催化剂中的手性立体中心在当前的对映选择性环氧化中起重要作用。此外,通过4c和7a显示的对映选择性的比较进一步证明了通过空间因子和手性中心在催化剂中的协同作用的显着影响。

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