DBU⋅HI 3 -catalyzed oxidative cyclization: An efficient route to flavones and azaflavones

An efficient and operationally simple protocol has been developed for the synthesis of biologically significant flavones and 2-arylquinolin-4-ones (azaflavones). The methodology utilizes a bench-stable organocatalyst, DBU⋅HI3, to drive the oxidative cyclization of substituted 2’-hydroxychalcones and 2’-aminochalcones. Optimization studies revealed that a 15 mol % catalyst loading in DMSO at 110 °C selectively promotes rapid dehydrogenative cyclization within 1-2.5 h, suppressing side products like flavanones. Conversely, protic or nonpolar solvents resulted in poor conversions or incomplete aromatization. This metal-free strategy tolerates a broad range of substrates, including electron-donating, electron-withdrawing, and selected heteroaryl groups, delivering the target frameworks in exceptional isolated yields (up to 94% for flavones and 91% for azaflavones). The synthesized products were structurally confirmed by spectroscopic analysis, and the efficient metal-free protocol provides a practical alternative to conventional transition-metal-based oxidative systems.

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Publication Details

Journal
Synthetic Communications
Published
2026-09-08
DOI
https://doi.org/10.1080/00397911.2026.2729564
Primary Topic
Synthesis of Organic Compounds
Type
article
Field-Weighted Citation Impact
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article

DBU⋅HI 3 -catalyzed oxidative cyclization: An efficient route to flavones and azaflavones

Ramesh Gawade, Pramod Kulkarni
Synthetic Communications
Synthesis of Organic Compounds
article

DBU⋅HI 3 -catalyzed oxidative cyclization: An efficient route to flavones and azaflavones

Ramesh Gawade, Pramod Kulkarni
article en

Abstract

An efficient and operationally simple protocol has been developed for the synthesis of biologically significant flavones and 2-arylquinolin-4-ones (azaflavones). The methodology utilizes a bench-stable organocatalyst, DBU⋅HI3, to drive the oxidative cyclization of substituted 2’-hydroxychalcones and 2’-aminochalcones. Optimization studies revealed that a 15 mol % catalyst loading in DMSO at 110 °C selectively promotes rapid dehydrogenative cyclization within 1-2.5 h, suppressing side products like flavanones. Conversely, protic or nonpolar solvents resulted in poor conversions or incomplete aromatization. This metal-free strategy tolerates a broad range of substrates, including electron-donating, electron-withdrawing, and selected heteroaryl groups, delivering the target frameworks in exceptional isolated yields (up to 94% for flavones and 91% for azaflavones). The synthesized products were structurally confirmed by spectroscopic analysis, and the efficient metal-free protocol provides a practical alternative to conventional transition-metal-based oxidative systems.

Synthetic Communications
Hans Raj Mahila Maha Vidyalaya (IN), Yaroslavl State Agricultural Academy (RU)
Openalex Percentile: Top 13%
Synthesis of Organic Compounds
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