From the journal:

Chemical Communications

A cyano-substituted phenoxazine moiety as an organophotoredox catalyst for C–C, C–B and C–P coupling reactions with aryl halides

Aditi Dasa  and  Chandan Mukherjee ORCID logo *a  

* Corresponding authors

a Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam, India
E-mail: cmukherjee@iitg.ac.in

Abstract

A phenoxazine-based organophotoredox catalyst, PC-A, reported to catalyze various C–C, C–B, and C–P bond-forming reactions with redox-inert substrates when excited at 395 nm.

Graphical abstract: A cyano-substituted phenoxazine moiety as an organophotoredox catalyst for C–C, C–B and C–P coupling reactions with aryl halides

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Article information

DOI
https://doi.org/10.1039/D6CC00635C
Article type
Communication
Submitted
30 Jan 2026
Accepted
01 Apr 2026
First published
02 Apr 2026

Chem. Commun., 2026, Advance Article

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A cyano-substituted phenoxazine moiety as an organophotoredox catalyst for C–C, C–B and C–P coupling reactions with aryl halides

A. Das and C. Mukherjee, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D6CC00635C

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