Formal Dehydrative [3+2] Annulation of <i>N</i> ‐Arylhydroxamine and Activated Alkyne Toward Indole

Abstract An efficient approach for the synthesis of indole by the annulation of N ‐substituted hydroxylamine with activated alkynes under mild reaction conditions was established without the additional catalyst or chemical reagents. Both 3‐substituted and 2,3‐disubstituted indoles were obtained with good‐to‐excellent isolated yields by using the terminal and internal electron‐deficient alkynes, respectively. This novel and green protocol provides a rapid, mild, and efficient method for the construction of indole heterocycles.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-05-20
DOI
https://doi.org/10.1002/ajoc.202500405
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Formal Dehydrative [3+2] Annulation of N ‐Arylhydroxamine and Activated Alkyne Toward Indole

Lanqin Liu, Shaoqun Zhu, Hong Hou, Huaguang Yu et al.
1 citations
Asian Journal of Organic Chemistry
Catalytic Alkyne Reactions
0.94
article

Formal Dehydrative [3+2] Annulation of N ‐Arylhydroxamine and Activated Alkyne Toward Indole

Lanqin Liu, Shaoqun Zhu, Hong Hou, Huaguang Yu, Xiaoyan Hong, Ying Han
article en
1 citations

Abstract

Abstract An efficient approach for the synthesis of indole by the annulation of N ‐substituted hydroxylamine with activated alkynes under mild reaction conditions was established without the additional catalyst or chemical reagents. Both 3‐substituted and 2,3‐disubstituted indoles were obtained with good‐to‐excellent isolated yields by using the terminal and internal electron‐deficient alkynes, respectively. This novel and green protocol provides a rapid, mild, and efficient method for the construction of indole heterocycles.

Asian Journal of Organic ChemistryVol. 14(8)
Jianghan University (CN), Yangzhou University (CN)
Natural Science Research of Jiangsu Higher Education Institutions of China
Openalex Percentile: Top 26%
Catalytic Alkyne Reactions
0.94
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