Access to Divergent Indolyl Pyrrolones via [3+2] Annulation of Indolyl Hydroxamates with Phosphonium Ylides

We report a novel [3+2] cycloaddition strategy between indolyl hydroxamates and phosphonium ylides, which selectively constructs three distinct N-heterocycles: indolyl maleimides, 5-methylenepyrrolones, and 5-hydroxypyrrolones. Notably, this work reveals the unprecedented role of phosphonium ylides as two-carbon synthons in the N-heterocycle formation.

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Publication Details

Journal
Organic Letters
Published
2025-10-23
DOI
https://doi.org/10.1021/acs.orglett.5c03964
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Access to Divergent Indolyl Pyrrolones via [3+2] Annulation of Indolyl Hydroxamates with Phosphonium Ylides

Xin Tang, Lixian Shen, Yao‐Fu Zeng, Zhen Wang et al.
1 citations
Organic Letters
Catalytic C–H Functionalization Methods
0.94
article

Access to Divergent Indolyl Pyrrolones via [3+2] Annulation of Indolyl Hydroxamates with Phosphonium Ylides

Xin Tang, Lixian Shen, Yao‐Fu Zeng, Zhen Wang, Zhang Chen, Jinjin Chen, Yao Tian, Dong-Xiao Jiang, Wei Zhang
article en
1 citations

Abstract

We report a novel [3+2] cycloaddition strategy between indolyl hydroxamates and phosphonium ylides, which selectively constructs three distinct N-heterocycles: indolyl maleimides, 5-methylenepyrrolones, and 5-hydroxypyrrolones. Notably, this work reveals the unprecedented role of phosphonium ylides as two-carbon synthons in the N-heterocycle formation.

Organic LettersVol. 27(43)
Qinghai Tibetan Hospital (CN), Hunan Vocational Institute of Technology (CN), Hengyang Academy of Agricultural Sciences (CN), Department of Science and Technology of Hunan Province (CN), University of South China (CN)
Openalex Percentile: Top 20%
Catalytic C–H Functionalization Methods
0.94
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