Visible Light-Induced Cyclization of <i>N</i> -Arylmethacrylohydrazides and Hydroxamic Acid Derivatives toward δ-Amidoalkylated Pyrazol-5-ones via 1,5-Hydrogen Atom Transfer

A photoinduced radical cascade cyclization of <i>N</i>-arylmethacrylohydrazides and hydroxamic acid derivatives for the synthesis of pyrazol-5-ones via 1,5-hydrogen atom transfer was developed. A series of pyrazol-5-ones was obtained in good yield with a broad substrate scope and excellent functional group compatibility. The procedure was also applied to the late-stage modification of natural products and drug molecules.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-01-21
DOI
https://doi.org/10.1021/acs.joc.5c03039
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Visible Light-Induced Cyclization of N -Arylmethacrylohydrazides and Hydroxamic Acid Derivatives toward δ-Amidoalkylated Pyrazol-5-ones via 1,5-Hydrogen Atom Transfer

Yangjian Cheng, Guocheng Yin, Jin-Tao Yu
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Visible Light-Induced Cyclization of N -Arylmethacrylohydrazides and Hydroxamic Acid Derivatives toward δ-Amidoalkylated Pyrazol-5-ones via 1,5-Hydrogen Atom Transfer

Yangjian Cheng, Guocheng Yin, Jin-Tao Yu
article en

Abstract

A photoinduced radical cascade cyclization of <i>N</i>-arylmethacrylohydrazides and hydroxamic acid derivatives for the synthesis of pyrazol-5-ones via 1,5-hydrogen atom transfer was developed. A series of pyrazol-5-ones was obtained in good yield with a broad substrate scope and excellent functional group compatibility. The procedure was also applied to the late-stage modification of natural products and drug molecules.

The Journal of Organic ChemistryVol. 91(4)
Changzhou University (CN)
Openalex Percentile: Top 82%
Radical Photochemical Reactions
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