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Table · dataset · 2026

Visible-Light-Induced Dearomative Heteroarylation of Anthracene Derivatives with Heteroarylnitriles via Combined Energy Transfer and Electron Transfer

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.1021/acs.orglett.6c03894.s001

The introduction of nitrogen-containing heterocycles, especially pyridine rings, into polycyclic compounds is expected to enhance their antimicrobial activities and modulate their fluorescence properties.

Description

A novel visible-light-induced dearomative heteroarylation of anthracenes with cyanoarenes has been developed. Combining energy transfer processes with electron transfer processes enables the generation of radical anion intermediates, which could sequentially undergo radical–radical coupling for the introduction of heteroaryl groups.

This method was compatible with various polycyclic arenes and cyanoarenes with excellent functional group tolerance and high yields.

Links

Where it is published

Catalogue records · 1

Topics

Provenance · 3 source records, 35 field assertions
SourceKeyLast seenRaw
ZivaHuboai:figshare.com:article/3403788711 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3403788711 d agoJSON v1
DMU Figshareoai:figshare.com:article/3403788711 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[field].anzsrc:field:320211mapping · zivahub uct ac zavocabulary-mapper@1.0.0keywords['Infectious Diseases']
concepts[field].anzsrc:field:320211mapping · dro deakin edu auvocabulary-mapper@1.0.0keywords['Infectious Diseases']
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