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α-Chloroketones enabled Rh(Ⅲ)-catalyzed enantioselective C-H[4+2]annulation of sulfoximines under mild and redox-neutral conditions

Qingwei Song Wenhao Wu Weijie Chen Hui Gao Zhi Zhou Zhongyi Zeng Wei Yi

Green Synthesis and Catalysis2025，Vol.6Issue(3)：P.320-323,4.

Green Synthesis and Catalysis2025，Vol.6Issue(3)：P.320-323,4.DOI:10.1016/j.gresc.2024.05.004

α-Chloroketones enabled Rh(Ⅲ)-catalyzed enantioselective C-H[4+2]annulation of sulfoximines under mild and redox-neutral conditions

Qingwei Song ¹Wenhao Wu ¹Weijie Chen ¹Hui Gao ¹Zhi Zhou ¹Zhongyi Zeng ¹Wei Yi¹

作者信息

1. Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target&Clinical Pharmacology,The NMPA and State Key Laboratory of Respiratory Disease,School of Pharmaceutical Sciences and the Fifth Affiliated Hospital,Guangzhou Medical University,Guangzhou 511436,China
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摘要

关键词

Sulfoximines/α-Chloroketones/Enantioselectivity/C-H functionalization/Rhodium catalysis

分类

化学化工

引用本文复制引用

Qingwei Song,Wenhao Wu,Weijie Chen,Hui Gao,Zhi Zhou,Zhongyi Zeng,Wei Yi..α-Chloroketones enabled Rh(Ⅲ)-catalyzed enantioselective C-H[4+2]annulation of sulfoximines under mild and redox-neutral conditions[J].Green Synthesis and Catalysis,2025,6(3):P.320-323,4.

基金项目

the National Natural Science Foundation of China(Nos.82273795 and 22201051) （Nos.82273795 and 22201051）

Science and Technology Program of Guangzhou(No.2023A04J0074) （No.2023A04J0074）

Plan on Enhancing Scientific Research at GMU for financial support on this research. （）

Green Synthesis and Catalysis

ISSN：2666-5549

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