| Literature DB >> 30589183 |
Zhong-Jian Cai1, Chen-Xu Liu1, Qing Gu1, Chao Zheng1, Shu-Li You1,2.
Abstract
Asymmetric C-H bond functionalization reaction is one of the most efficient and straightforward methods for the synthesis of optically active molecules. Herein we disclose an asymmetric C-H/C-H cross-coupling reaction of ferrocenes with azoles such as oxazoles and thiazoles. Palladium(II)/monoprotected amino acid (MPAA) catalytic system which exhibits excellent reactivity and regioselectivity for oxazoles and thiazoles. This method offers a powerful strategy for constructing planar chiral ferrocenes. Mechanistic studies suggest that the C-H bond cleavage of azoles is likely proceeding through a SE Ar process and may not be a turnover limiting step.Entities:
Keywords: C−H activation; asymmetric catalysis; azole; ferrocene; regioselectivity
Year: 2019 PMID: 30589183 DOI: 10.1002/anie.201813887
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336