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Ligand-controlled switch in diastereoselectivities: catalytic asymmetric construction of spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives.

作者信息

Deng Hua, Jia Renmeng, Yang Wu-Lin, Yu Xingxin, Deng Wei-Ping

机构信息

School of Pharmacy and Shanghai Key Laboratory of New Drug Design, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, People's Republic of China.

出版信息

Chem Commun (Camb). 2019 Jun 20;55(51):7346-7349. doi: 10.1039/c9cc03589c.

DOI:10.1039/c9cc03589c
PMID:31169844
Abstract

An efficient catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides with four-membered ring-containing exocyclic alkenes has been developed, and either the exo or endo spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives were diastereodivergently generated by employing Cu(i)/tBu-Phosferrox and a Cu(i)/N,O-ligand complex, respectively. Notably, various heteroatom-containing (N, O, S) exocyclic alkenes were found to be well-tolerated in this transformation.

摘要

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