Development of efficient solid chiral catalysts with designable linkage for asymmetric transfer hydrogenation of quinoline derivatives
| Autor: | Yiqi Ren, Qihua Yang, Lin Tao, He Li, Chunzhi Li, Sanjeevi Jayakumar |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Quinoline
Enantioselective synthesis Homogeneous catalysis 02 engineering and technology General Medicine 010402 general chemistry 021001 nanoscience & nanotechnology Transfer hydrogenation 01 natural sciences Combinatorial chemistry 0104 chemical sciences Catalysis Reaction rate chemistry.chemical_compound chemistry Ionic liquid 0210 nano-technology Mesoporous material |
| Zdroj: | Chinese Journal of Catalysis. 42:1576-1585 |
| ISSN: | 1872-2067 |
| DOI: | 10.1016/s1872-2067(20)63764-0 |
| Popis: | Developing chiral solid catalysts for asymmetric catalysis is desirable for the elimination of homogeneous catalysis flaws but remains an immense challenge. Herein, we report the immo-bilization of TsDPEN on SBA-15 with an ionic liquid (IL) linkage via the one-pot reac-tion of imidazole-TsDPEN-N-Boc with 3-(trimethoxysilyl)propyl bromide in the SBA-15 mesopores. After coordination to Rh, the chiral solid catalysts could efficiently cata-lyze quinoline transfer hydrogenation, achieving 97% conversion with 93% ee, which was comparable to their homogeneous counterparts. The chiral solid catalyst with the IL linkage afforded much higher turnover frequency than that without the IL linkage (93 h–1 vs. 33 h–1), attributed to the phase transfer and formate-enriching ability of the IL linkage. Furthermore, the effect of the pH on the reaction rate of the solid catalyst was in-vestigated, preventing reaction rate retardation during the catalytic process. The tuning of the linkage group is an efficient approach for catalytic activity improvement of immobilized chiral catalysts. |
| Databáze: | OpenAIRE |
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