Synthesis of Eight‐Membered Carbocycle‐Fused 1,2,3‐Triazole Scaffolds via Palladium‐Catalyzed Tandem Reactions and Michael Addition

Both eight‐membered carbocyclic rings and 1,2,3‐triazole rings represent vital structural motifs. In this article, we present a Pd‐catalyzed tandem reaction that facilitates the synthesis of fused eight membered carbocyclic ring‐fused 1,2,3‐triazole derivatives from 2‐iodophenyl‐enones and propargylic ethers bearing azidophenyl group. Furthermore, we show that TBD plays a pivotal role as a mediator in converting the Sonogashira cross‐coupling intermediates into the desired products.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-16
DOI
https://doi.org/10.1002/ejoc.70396
Primary Topic
Click Chemistry and Applications
Type
article
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article

Synthesis of Eight‐Membered Carbocycle‐Fused 1,2,3‐Triazole Scaffolds via Palladium‐Catalyzed Tandem Reactions and Michael Addition

Ruwei Shen, Shugao Zhu, Yuxuan Fang, Xinxin Chen et al.
European Journal of Organic Chemistry
Click Chemistry and Applications
article

Synthesis of Eight‐Membered Carbocycle‐Fused 1,2,3‐Triazole Scaffolds via Palladium‐Catalyzed Tandem Reactions and Michael Addition

Ruwei Shen, Shugao Zhu, Yuxuan Fang, Xinxin Chen, Yu Xin, Bin Liu
article en

Abstract

Both eight‐membered carbocyclic rings and 1,2,3‐triazole rings represent vital structural motifs. In this article, we present a Pd‐catalyzed tandem reaction that facilitates the synthesis of fused eight membered carbocyclic ring‐fused 1,2,3‐triazole derivatives from 2‐iodophenyl‐enones and propargylic ethers bearing azidophenyl group. Furthermore, we show that TBD plays a pivotal role as a mediator in converting the Sonogashira cross‐coupling intermediates into the desired products.

European Journal of Organic Chemistry
Nanjing Tech University (CN), Nanchang University (CN)
Openalex Percentile: Top 12%
Click Chemistry and Applications
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