Desymmetrization–Addition Reaction of Cyclopropenes to Imines via Synergistic Photoredox and Cobalt Catalysis

Herein, we designed a reaction for the desymmetrization–addition of cyclopropenes to imines by leveraging the synergy between photoredox and asymmetric cobalt catalysis. This protocol facilitated the synthesis of a series of chiral functionalized cyclopropanes with high yield, enantioselectivity, an...

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Veröffentlicht in:Journal of the American Chemical Society 2024-07, Vol.146 (28), p.18892-18898
Hauptverfasser: He, Xiang-Kui, Lu, Liang-Qiu, Yuan, Bao-Ru, Luo, Jia-Long, Cheng, Ying, Xiao, Wen-Jing
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Sprache:eng
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Zusammenfassung:Herein, we designed a reaction for the desymmetrization–addition of cyclopropenes to imines by leveraging the synergy between photoredox and asymmetric cobalt catalysis. This protocol facilitated the synthesis of a series of chiral functionalized cyclopropanes with high yield, enantioselectivity, and diastereoselectivity (44 examples, up to 93% yield and >99% ee). A possible reaction mechanism involving cyclopropene desymmetrization by Co–H species and imine addition by Co-alkyl species was proposed. This study provides a novel route to important chiral cyclopropanes and extends the frontier of asymmetric metallaphotoredox catalysis.
ISSN:0002-7863
1520-5126
1520-5126
DOI:10.1021/jacs.4c07096