Ag‐Catalyzed Selective <scp>C1</scp> ‐Acylation of Pyrrolo[1,2‐ <i>a</i> ]Quinoxalines With 2‐Oxo‐2‐Arylacetic Acids

ABSTRACT A silver‐catalyzed decarboxylative acylation protocol has been developed for the direct C1H functionalization of pyrrolo[1,2‐ a ]quinoxalines using α ‐oxocarboxylic acids as bench‐stable acyl precursors. A variety of aryl(pyrrolo[1,2‐ a ]quinoxalin‐1‐yl)methanone derivatives were synthesized with good yields. In this process, α ‐oxocarboxylic acids serve as efficient acylation reagents, generating the desired reactive acyl carbocation in situ. The methodology demonstrates excellent regioselectivity and scalability to gram–level production, which facilitated the molecular diversity of pyrrolo[1,2‐ a ]quinoxaline by allowing convenient functionalization at the C3–position.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2026-01-12
DOI
https://doi.org/10.1002/jhet.70160
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Ag‐Catalyzed Selective C1 ‐Acylation of Pyrrolo[1,2‐ a ]Quinoxalines With 2‐Oxo‐2‐Arylacetic Acids

Wanqiang Wang, Jin Zhang, Jing He, Ping Liu et al.
Journal of Heterocyclic Chemistry
Catalytic C–H Functionalization Methods
article

Ag‐Catalyzed Selective C1 ‐Acylation of Pyrrolo[1,2‐ a ]Quinoxalines With 2‐Oxo‐2‐Arylacetic Acids

Wanqiang Wang, Jin Zhang, Jing He, Ping Liu, Yingqian Li
article en

Abstract

ABSTRACT A silver‐catalyzed decarboxylative acylation protocol has been developed for the direct C1H functionalization of pyrrolo[1,2‐ a ]quinoxalines using α ‐oxocarboxylic acids as bench‐stable acyl precursors. A variety of aryl(pyrrolo[1,2‐ a ]quinoxalin‐1‐yl)methanone derivatives were synthesized with good yields. In this process, α ‐oxocarboxylic acids serve as efficient acylation reagents, generating the desired reactive acyl carbocation in situ. The methodology demonstrates excellent regioselectivity and scalability to gram–level production, which facilitated the molecular diversity of pyrrolo[1,2‐ a ]quinoxaline by allowing convenient functionalization at the C3–position.

Journal of Heterocyclic Chemistry
Shihezi University (CN)
Openalex Percentile: Top 90%
Catalytic C–H Functionalization Methods
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