A Metal-Catalyzed Tunable Reaction of Ylides with Hydroxylamine Derivatives

In this work, a tunable reaction of metal acyl nitrene with ylides is reported for the divergent synthesis of enamides and α,α-dicarbonyl phosphorus ylides. The reaction is featured with mild conditions, good reaction efficiency, and broad reaction generality. In particular, the resulting enamides could be structurally elaborated into potential useful scaffolds. Mechanism investigation suggests that the formation of enamides was ascribed to the nucleophilic substitution of ferric nitrene with sulfur ylides. It is believed that this reaction represents an initial example of preparing enamides from iron-catalyzed nitrene transfer.

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Publication Details

Journal
Organic Letters
Published
2025-03-25
DOI
https://doi.org/10.1021/acs.orglett.5c00576
Citations
1
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.94

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A Metal-Catalyzed Tunable Reaction of Ylides with Hydroxylamine Derivatives

Guanyinsheng Qiu, N. F. Chen, Honglin Song, Ming Hou et al.
1 citations
Organic Letters
Cyclopropane Reaction Mechanisms
0.94
article

A Metal-Catalyzed Tunable Reaction of Ylides with Hydroxylamine Derivatives

Guanyinsheng Qiu, N. F. Chen, Honglin Song, Ming Hou, Banpeng Cao
article en
1 citations

Abstract

In this work, a tunable reaction of metal acyl nitrene with ylides is reported for the divergent synthesis of enamides and α,α-dicarbonyl phosphorus ylides. The reaction is featured with mild conditions, good reaction efficiency, and broad reaction generality. In particular, the resulting enamides could be structurally elaborated into potential useful scaffolds. Mechanism investigation suggests that the formation of enamides was ascribed to the nucleophilic substitution of ferric nitrene with sulfur ylides. It is believed that this reaction represents an initial example of preparing enamides from iron-catalyzed nitrene transfer.

Organic LettersVol. 27(13)
Jiangxi Science and Technology Normal University (CN), Jiaxing University (CN), Institute of Organic Chemistry (HU)
National Natural Science Foundation of China
Openalex Percentile: Top 28%
Cyclopropane Reaction Mechanisms
0.94
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