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Table · dataset · 2026

Photo-Induced Three-Component Radical Trifluoromethylation/Heteroarylation of Alkenes via EDA Complexes

Listed in figshare and Loughborough Research Repository — shown once because both records carry DOI 10.1021/acs.joc.6c01316.s001

This study develops a visible-light-induced electron donor–acceptor (EDA) complex strategy, employing the inexpensive and readily available DBU as the electron donor and the industrially available CF<sub>3</sub>Br as the trifluoromethyl source, to achieve the trifluoromethylation/heteroarylation of alkenes.

Description

This method offers advantages in cost-effectiveness and facile postreaction processing, without requiring transition metals or fluorescent dyes as photocatalysts.

Moreover, nitrogen-containing heterocycles such as quinoxalinones, uracils, and pyrazines are all compatible in this transformation through C–H alkylation, providing a convenient and economical new avenue for the green late-stage modification of nitrogen-containing heterocyclic compounds.

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Where it is published

Catalogue records · 1

Topics

Provenance · 2 source records, 34 field assertions
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figshareoai:figshare.com:article/339954238 d agoJSON v1
Loughborough Research Repositoryoai:figshare.com:article/339954238 d agoJSON v1
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