z-logo
Premium
Acyl Radicals from Aromatic Carboxylic Acids by Means of Visible‐Light Photoredox Catalysis
Author(s) -
Bergonzini Giulia,
Cassani Carlo,
Wallentin CarlJohan
Publication year - 2015
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201506432
Subject(s) - radical , reagent , chemistry , photoredox catalysis , catalysis , photochemistry , visible spectrum , tin , redox , carboxylic acid , irradiation , organic chemistry , photocatalysis , materials science , optoelectronics , physics , nuclear physics
Simple and abundant carboxylic acids have been used as acyl radical precursor by means of visible‐light photoredox catalysis. By the transient generation of a reactive anhydride intermediate, this redox‐neutral approach offers a mild and rapid entry to high‐value heterocyclic compounds without the need of UV irradiation, high temperature, high CO pressure, tin reagents, or peroxides.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here