Abstract
Transition-metal-catalyzed direct activation reactions of unreactive C-H bond has been extensively developed in recent years. Although numerous synthetic methods have been reported to build diverse complex compounds, enantioselective C-H activation has not been paid much attention probably because of the absence of suitable ligands to control the stereoselectivity in the C-H activation reaction. Herein, a Pd(0)-catalyzed enantioselective synthesis of planar chiral ferrocenes was described, and chiral phosphoric acids were used as the only chiral source to control the stereoselectivity in the C-H activation reactions.
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Zhang, S., Lu, J., Ye, J., & Duan, W. L. (2016). Asymmetric C-H arylation for the synthesis of planar chiral ferrocenes: Controlling enantioselectivity using chiral phosphoric acids. Chinese Journal of Organic Chemistry, 36(4), 752–759. https://doi.org/10.6023/cjoc201602032
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