Recent Advances in Transformation of 1,4‐Diyn‐3‐ones and 1,4‐Diyn‐3‐ols

ABSTRACT 1,4‐Diyn‐3‐ones and 1,4‐diyn‐3‐ols have garnered considerable attention due to their distinctive characteristics, including multiple reaction sites. Numerous new reactions involving these compounds have been discovered in the past decades. Their transformations can provide a variety of useful O‐containing and N‐containing heterocycles with high regio‐ and stereoselectivity, including pyrones, pyrrolones, furans, and pyridones. In this review, we summarize the latest trends and developments of reactions involving 1,4‐diyn‐3‐ones and 1,4‐diyn‐3‐ols with a series of reagents including amines, water, N ‐oxides, 1,3‐dicarbonyl compounds, quinolines, isoxazoles, and so on. We highlight the product diversity, selectivity, and applicability of these transformations and, where possible, discuss the underlying mechanistic rationale.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-11-08
DOI
https://doi.org/10.1002/ajoc.202500627
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Recent Advances in Transformation of 1,4‐Diyn‐3‐ones and 1,4‐Diyn‐3‐ols

Qian Wang, Tao Wang
1 citations
Asian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Recent Advances in Transformation of 1,4‐Diyn‐3‐ones and 1,4‐Diyn‐3‐ols

Qian Wang, Tao Wang
article en
1 citations

Abstract

ABSTRACT 1,4‐Diyn‐3‐ones and 1,4‐diyn‐3‐ols have garnered considerable attention due to their distinctive characteristics, including multiple reaction sites. Numerous new reactions involving these compounds have been discovered in the past decades. Their transformations can provide a variety of useful O‐containing and N‐containing heterocycles with high regio‐ and stereoselectivity, including pyrones, pyrrolones, furans, and pyridones. In this review, we summarize the latest trends and developments of reactions involving 1,4‐diyn‐3‐ones and 1,4‐diyn‐3‐ols with a series of reagents including amines, water, N ‐oxides, 1,3‐dicarbonyl compounds, quinolines, isoxazoles, and so on. We highlight the product diversity, selectivity, and applicability of these transformations and, where possible, discuss the underlying mechanistic rationale.

Asian Journal of Organic ChemistryVol. 14(12)
Shaanxi Normal University (CN), Huizhou University (CN)
Openalex Percentile: Top 20%
Catalytic C–H Functionalization Methods
0.94
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