Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 1, Pages 156-158Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b919902k
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Funding
- NSFC [20632060, 20821002, 20620140429, 30772625]
- Chinese Academy of Sciences
- Major Basic Research Development Program of China [2010CB833300]
- Science and Technology Commission of Shanghai Municipality
- Merck Research Laboratories
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The enantioselective hydrogenation of a series of challenging substrates, alpha-aryl-beta-substituted acrylic acids, was realized with high efficiency and enantioselectivity (up to 96%) under the catalysis of Ir(I) complex of Spiro-based P,N ligand, SpinPHOX.
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