期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 61, 期 1, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202113052
关键词
asymmetric synthesis; dihydrosilanes; hydrosilylation; monohydrosilane; rhodium
资金
- National Natural Science Foundation of China [22171277, 22101291, 21821002, 21890722, 21950410519]
- Shanghai Rising-Star Program [20QA1411400]
- Natural Science Foundation of Tianjin Municipality [19JCJQJC62300]
- Tianjin Research Innovation Project for Postgraduate Students [2019YJSB081]
- Frontiers Science Center for New Organic Matter [Nankai University] [63181206]
- Shanghai Institute of Organic Chemistry, State Key Laboratory of Organometallic Chemistry
This study demonstrated an asymmetric synthesis method for monohydrosilanes via intramolecular hydrosilylation strategy, with high diastereo-, regio-, and enantioselectivities, including chiral oxasilacycles. The catalyst loading could be reduced to 0.1 mol %, making it one of the most efficient methods for accessing chiral monohydrosilanes. Mechanistic studies suggest a Chalk-Harrod mechanism for the Rh-catalyzed intramolecular asymmetric hydrosilylation reaction.
Enantiopure monohydrosilanes are versatile chiral reagents for alcohol resolution and mechanistic investigation. Herein, we have demonstrated the asymmetric synthesis of monohydrosilanes via an intramolecular hydrosilylation strategy. This protocol is suitable for the synthesis of five- and six-membered cyclic monohydrosilanes, including a class of chiral oxasilacycles, with excellent diastereo-, regio-, and enantioselectivities. Notably, the catalyst loading could be reduced to 0.1 mol % which makes this one of the most efficient methods to access chiral monohydrosilanes. Mechanistic studies and DFT calculations indicate this Rh-catalyzed intramolecular asymmetric hydrosilylation reaction might proceed via a Chalk-Harrod mechanism, and the enantio-determining step was predicted to be oxidative addition of Si-H bond.
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