Photoredox-Catalysed Decarboxylative Alkylation of N-Heteroarenes with N-(Acyloxy)phthalimides.

Chemistry

Hefei National Laboratory for Physical Sciences at the Microscale, iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei, 230026, P. R. China.

Published: February 2017

An iridium photoredox catalyst in combination with either a stoichiometric amount of Brønsted acid or a catalytic amount of Lewis acid is capable of catalyzing regioselective alkylation of N-heteroarenes with N-(acyloxy)phthalimides at room temperature under irradiation. A broad range of N-heteroarenes can be alkylated using a variety of secondary, tertiary, and quaternary carboxylates. Mechanistic studies suggest that an Ir /Ir redox catalytic cycle is responsible for the observed reactivity.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.201605640DOI Listing

Publication Analysis

Top Keywords

alkylation n-heteroarenes
8
n-heteroarenes n-acyloxyphthalimides
8
photoredox-catalysed decarboxylative
4
decarboxylative alkylation
4
n-acyloxyphthalimides iridium
4
iridium photoredox
4
photoredox catalyst
4
catalyst combination
4
combination stoichiometric
4
stoichiometric amount
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!