Computational studies on Mn(<scp>iii</scp>)-catalyzed cyclopropanols: a case of Mn(<scp>iii</scp>)-based metalloradical catalysis involving an α-Mn(<scp>ii</scp>)-bound-alkyl radical key intermediate

Substrates that generate metal-bound radical species have predominantly been oxidative in nature. In this study, we present cyclopropanol, a reducing substrate, capable of generating metal-bound radicals through a Mn(acac) 3 catalyst.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-12-11
DOI
https://doi.org/10.1039/d4qo01775g
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
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Computational studies on Mn(iii)-catalyzed cyclopropanols: a case of Mn(iii)-based metalloradical catalysis involving an α-Mn(ii)-bound-alkyl radical key intermediate

Long‐Wu Ye, Xin Lu, Yidong Luo, Xiuyuan Zou et al.
Organic Chemistry Frontiers
Oxidative Organic Chemistry Reactions
article

Computational studies on Mn(iii)-catalyzed cyclopropanols: a case of Mn(iii)-based metalloradical catalysis involving an α-Mn(ii)-bound-alkyl radical key intermediate

Long‐Wu Ye, Xin Lu, Yidong Luo, Xiuyuan Zou, Hong Pan, Qing Sun, Pengcheng Zhang
article en

Abstract

Substrates that generate metal-bound radical species have predominantly been oxidative in nature. In this study, we present cyclopropanol, a reducing substrate, capable of generating metal-bound radicals through a Mn(acac) 3 catalyst.

Organic Chemistry FrontiersVol. 12(3)
Xiamen University (CN), Zhoukou Normal University (CN), Institute of New Materials (CN), Nanchang Hangkong University (CN)
Openalex Percentile: Top 83%
Oxidative Organic Chemistry Reactions
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Computational studies on Mn(<scp>iii</scp>)-catalyzed cyclopropanols: a case of Mn(<scp>iii</scp>)-based metalloradical catalysis involving an α-Mn(<scp>ii</scp>)-bound-alkyl radical key intermediate — Long‐Wu Ye, Xin Lu, et al. · Organic Chemistry Frontiers (2024) | TGRS Research Map | TGRS