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通过不对称三反应序列对具有五个连续手性中心的多环吲唑骨架进行对映选择性构建。

Enantioselective Construction of Polycyclic Indazole Skeletons Bearing Five Consecutive Chiral Centers through an Asymmetric Triple-Reaction Sequence.

作者信息

Zhang Jia-Lu, Ye Wen-Long, Zhang Jie, Hu Xiu-Qin, Xu Peng-Fei

机构信息

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.

出版信息

Org Lett. 2021 Jul 2;23(13):5033-5038. doi: 10.1021/acs.orglett.1c01559. Epub 2021 Jun 17.

DOI:10.1021/acs.orglett.1c01559
PMID:34138570
Abstract

A novel approach for the asymmetric construction of polycyclic indazole skeletons via enamine-imine activation and PCET activation was developed by merging organocatalysis with photocatalysis through an asymmetric triple-reaction sequence. In this process, five C-X bonds and five consecutive chiral centers were efficiently constructed. Differently substituted polycyclic indazole deriatives were successfully constructed with satisfactory results under mild conditions.

摘要

通过将有机催化与光催化通过不对称三反应序列相结合,开发了一种通过烯胺-亚胺活化和PCET活化不对称构建多环吲唑骨架的新方法。在此过程中,高效构建了五个C-X键和五个连续的手性中心。在温和条件下成功构建了不同取代的多环吲唑衍生物,结果令人满意。

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