Visible Light-Induced\nRadical Cascade Functionalization\nof Quinoxalin-2(1<i>H</i>)‑ones: Three-Component\n1,2-Di(hetero)arylation Approach with Styrenes and Thianthrenium Salts

The\nadditive-free visible light-induced three-component 1,2-di(hetero)arylation\nof styrenes was developed using quinoxalin-2(1<i>H</i>)-ones\nand thianthrenium salts. The purple visible light excitable quinoxalin-2(1<i>H</i>)-ones were utilized for the single-electron transfer to\naryl thianthrenium salts, where the generated aryl radical species\nunderwent the addition cascade to styrenes and quinoxalin-2(1<i>H</i>)-ones. The direct aryl radical addition to quinoxalin-2(1<i>H</i>)-ones also led to the formation of a side product, C3-aryl\nquinoxalin-2(1<i>H</i>)-ones, capable of a photoredox process\nto help the formation of 1,2-di(hetero)arylation products.

Publication Details

Journal
Figshare
Published
2024-10-09
DOI
https://doi.org/10.1021/acs.orglett.4c03565.s001
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visible Light-Induced\nRadical Cascade Functionalization\nof Quinoxalin-2(1H)‑ones: Three-Component\n1,2-Di(hetero)arylation Approach with Styrenes and Thianthrenium Salts

Figshare
Radical Photochemical Reactions
article

Visible Light-Induced\nRadical Cascade Functionalization\nof Quinoxalin-2(1H)‑ones: Three-Component\n1,2-Di(hetero)arylation Approach with Styrenes and Thianthrenium Salts

article en

Abstract

The\nadditive-free visible light-induced three-component 1,2-di(hetero)arylation\nof styrenes was developed using quinoxalin-2(1<i>H</i>)-ones\nand thianthrenium salts. The purple visible light excitable quinoxalin-2(1<i>H</i>)-ones were utilized for the single-electron transfer to\naryl thianthrenium salts, where the generated aryl radical species\nunderwent the addition cascade to styrenes and quinoxalin-2(1<i>H</i>)-ones. The direct aryl radical addition to quinoxalin-2(1<i>H</i>)-ones also led to the formation of a side product, C3-aryl\nquinoxalin-2(1<i>H</i>)-ones, capable of a photoredox process\nto help the formation of 1,2-di(hetero)arylation products.

Figshare
Openalex Percentile: Top 79%
Radical Photochemical Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.