Synthesis of isoquinolin-1,4-diones <i>via</i> photocatalytic C(sp <sup>2</sup> )–C(sp <sup>3</sup> )-scission/oxidation of 4-(hydroxy(aryl)methyl)-isoquinolin-1(2 <i>H</i> )-ones

Dihydroisoquinolin-1,4-diones represent an important class of nitrogen-containing fused heterocyclic units. Their straightforward synthesis from readily available precursors would be attractive. Herein, we present a novel photocatalytic method enabling the direct synthesis of diverse 3-methoxy-2,3-dihydroisoquinoline-1,4-diones from 4-(hydroxy(aryl)methyl)-isoquinolin-1(2<i>H</i>)-ones. The method demonstrates high functional group tolerance, enabling further synthetic transformations for isoquinoline-1,4-diones containing C3 quaternary carbon centers.

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Journal
Chemical Communications
Published
2026-01-01
DOI
https://doi.org/10.1039/d5cc03799a
Primary Topic
Synthesis and Biological Activity
Type
article
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article

Synthesis of isoquinolin-1,4-diones via photocatalytic C(sp 2 )–C(sp 3 )-scission/oxidation of 4-(hydroxy(aryl)methyl)-isoquinolin-1(2 H )-ones

Jiangbin Huang
Chemical Communications
Synthesis and Biological Activity
article

Synthesis of isoquinolin-1,4-diones via photocatalytic C(sp 2 )–C(sp 3 )-scission/oxidation of 4-(hydroxy(aryl)methyl)-isoquinolin-1(2 H )-ones

Jiangbin Huang
article en

Abstract

Dihydroisoquinolin-1,4-diones represent an important class of nitrogen-containing fused heterocyclic units. Their straightforward synthesis from readily available precursors would be attractive. Herein, we present a novel photocatalytic method enabling the direct synthesis of diverse 3-methoxy-2,3-dihydroisoquinoline-1,4-diones from 4-(hydroxy(aryl)methyl)-isoquinolin-1(2<i>H</i>)-ones. The method demonstrates high functional group tolerance, enabling further synthetic transformations for isoquinoline-1,4-diones containing C3 quaternary carbon centers.

Chemical CommunicationsVol. 62(11)
Wuyi University (CN)
Openalex Percentile: Top 96%
Synthesis and Biological Activity
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