Zn‐Catalyzed Cycloisomerization/Methylenation of Enyone with Vinyl Azide: Assembly of Terminal and Deuterated Alkenyl Furan Framework

An unprecedented zinc‐catalyzed cycloisomerization/methylenation reaction of enynone with vinyl azide is developed. Featuring inexpensive, less‐toxic catalyst, high efficiency, and mild reaction conditions, this protocol provides a practical synthetic method to access various bioactivity‐related terminal and deuterated alkenyl furans in up to 99% yield and 94% level of deuterium incorporation. The reaction is proposed to proceed through cycloisomerization, cyclopropanation, and ring fragmentation processes. Utility of this reaction is further demonstrated by transformation of the obtained molecules into selectively semi‐deuterated and non‐deuterated furan skeletons.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-09-09
DOI
https://doi.org/10.1002/adsc.70112
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87

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article

Zn‐Catalyzed Cycloisomerization/Methylenation of Enyone with Vinyl Azide: Assembly of Terminal and Deuterated Alkenyl Furan Framework

Jiangan Liu, Changyuan Zhang, Danling Tang, Hu Zhou et al.
2 citations
Advanced Synthesis & Catalysis
Cyclopropane Reaction Mechanisms
1.87
article

Zn‐Catalyzed Cycloisomerization/Methylenation of Enyone with Vinyl Azide: Assembly of Terminal and Deuterated Alkenyl Furan Framework

Jiangan Liu, Changyuan Zhang, Danling Tang, Hu Zhou, Shaotong Qiu, Y. Mao, Zhicheng Yang
article en
2 citations

Abstract

An unprecedented zinc‐catalyzed cycloisomerization/methylenation reaction of enynone with vinyl azide is developed. Featuring inexpensive, less‐toxic catalyst, high efficiency, and mild reaction conditions, this protocol provides a practical synthetic method to access various bioactivity‐related terminal and deuterated alkenyl furans in up to 99% yield and 94% level of deuterium incorporation. The reaction is proposed to proceed through cycloisomerization, cyclopropanation, and ring fragmentation processes. Utility of this reaction is further demonstrated by transformation of the obtained molecules into selectively semi‐deuterated and non‐deuterated furan skeletons.

Advanced Synthesis & CatalysisVol. 367(17)
Hunan University of Science and Technology (CN), Yichun University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Openalex Percentile: Top 13%
Cyclopropane Reaction Mechanisms
1.87
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