Synthesis and evaluation of Naphthalene-1, 8-dithiolate chelating ruthenium carbene catalyst for Z-Stereoretentive olefin metathesis

被引:5
作者
Wang, Tao [1 ,2 ]
Xie, Qingxiao [1 ,2 ]
Guo, Weijie [1 ,2 ]
Wu, Shutao [1 ,2 ]
Zhang, Huiqing [1 ,2 ]
Wang, Jianhui [1 ,2 ]
机构
[1] Tianjin Univ, Dept Chem, Coll Sci, Tianjin 300350, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 30072, Peoples R China
基金
中国国家自然科学基金;
关键词
Ruthenium carbene catalyst; Naphthalene-1,8-dithiolate chelating; Z-Stereoretentive; Cross-metathesis reactions; CLOSING ALKYNE METATHESIS; STEREOSELECTIVE-SYNTHESIS; CROSS-METATHESIS; COMPLEXES; EFFICIENT; POLYMERIZATION; MOLYBDENUM; DERIVATIVES; REACTIVITY; ALCOHOLS;
D O I
10.1016/j.jorganchem.2018.10.035
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A highly Z-stereoretentive olefin metathesis ruthenium carbene catalyst containing a naphthalene-1,8-dithiol ligand was synthesized, and the structure was determined by single-crystal X-ray diffraction. The new ruthenium carbene catalyst could catalyze cross-metathesis reactions of terminal alkenes with (Z)-but-2-ene-1,4-diol to give highly Z-stereoretentive products. Like to other ruthenium carbene catalysts, the new complex tolerates many different functional groups. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 67
页数:6
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