Issue 86, 2024

Phosphination of aryl/alkyl bromides via Mn-mediated reductive C–P coupling

Abstract

Mn-mediated reductive cross-coupling of organic bromides with 2-bromo-1,3,2-diazaphospholene was developed for efficient construction of C–P bonds under mild conditions. Mechanistic studies suggested that bromides are activated by in situ formed bis-diazaphospholene via hybrid radical and polar mechanisms.

Graphical abstract: Phosphination of aryl/alkyl bromides via Mn-mediated reductive C–P coupling

Supplementary files

Article information

Article type
Communication
Submitted
14 Sep 2024
Accepted
01 Oct 2024
First published
01 Oct 2024

Chem. Commun., 2024,60, 12549-12552

Phosphination of aryl/alkyl bromides via Mn-mediated reductive C–P coupling

L. Dong, B. Zhong, Y. Zhang, J. Yang and J. Cheng, Chem. Commun., 2024, 60, 12549 DOI: 10.1039/D4CC04750H

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