A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines

A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines leads to fluorinated naphtho[1',2':4,5]imidazo[1,2-<em>a</em>]pyridine-5,6-diones. Advantages of the proposed one-step procedure are easily available starting materials, atom economy, and simple isolation of products without chromatographic purification.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7737
Primary Topic
Bioactive Compounds and Antitumor Agents
Type
article
Field-Weighted Citation Impact
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article

A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines

E.V. Tretyakov, Boris V. Lichitsky, Ekaterina Kudryavtseva
Mendeleev Communications
Bioactive Compounds and Antitumor Agents
article

A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines

E.V. Tretyakov, Boris V. Lichitsky, Ekaterina Kudryavtseva
article en

Abstract

A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines leads to fluorinated naphtho[1',2':4,5]imidazo[1,2-<em>a</em>]pyridine-5,6-diones. Advantages of the proposed one-step procedure are easily available starting materials, atom economy, and simple isolation of products without chromatographic purification.

Mendeleev CommunicationsVol. 35(3)
N.D. Zelinsky Institute of Organic Chemistry (RU)
Openalex Percentile: Top 94%
Bioactive Compounds and Antitumor Agents
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