Annulation of Enyne-Amide with Enaminone Enables Divergent Synthesis of Furo[2,3-<i>b</i>]pyridine Derivatives

A wide range of furo[2,3-<i>b</i>]pyridine and furo[2,3-<i>b</i>]dihydropyridine derivatives, which might be of value in biomedicinal chemistry and materials science, are divergently delivered through Ag(I)-catalyzed tandem cycloisomerization/cyclization reactions between enyne-amides and enaminones just by tuning the reaction conditions. The products could be conveniently transformed into various derivatives.

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Publication Details

Journal
Organic Letters
Published
2025-07-20
DOI
https://doi.org/10.1021/acs.orglett.5c02452
Citations
2
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Annulation of Enyne-Amide with Enaminone Enables Divergent Synthesis of Furo[2,3-b]pyridine Derivatives

Xin Lv, Hui Mao, Hui Yang, Liejin Zhou et al.
2 citations
Organic Letters
Catalytic Alkyne Reactions
1.87
article

Annulation of Enyne-Amide with Enaminone Enables Divergent Synthesis of Furo[2,3-b]pyridine Derivatives

Xin Lv, Hui Mao, Hui Yang, Liejin Zhou, Zefeng Jin, Honglan Kang, Cuiying Li, Ziyan Ji
article en
2 citations

Abstract

A wide range of furo[2,3-<i>b</i>]pyridine and furo[2,3-<i>b</i>]dihydropyridine derivatives, which might be of value in biomedicinal chemistry and materials science, are divergently delivered through Ag(I)-catalyzed tandem cycloisomerization/cyclization reactions between enyne-amides and enaminones just by tuning the reaction conditions. The products could be conveniently transformed into various derivatives.

Organic LettersVol. 27(30)
Zhejiang Normal University (CN)
National Natural Science Foundation of China, Jinhua Science and Technology Bureau, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 14%
Catalytic Alkyne Reactions
1.87
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