Synthesis of Poly‐Substituted Imidazo[1,2‐ <i>a</i> ]Pyridines via a Double Annulation Strategy

Abstract A highly efficient domino process consisting of conjugate substitution, nucleophilic addition, and cycloisomerization from the reaction of enaminonitrile with propargylamine allowed for a successive double ring closure to afford a densely functionalized imidazo[1,2‐ a ]pyridine through formation of three C─N bonds.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-08-25
DOI
https://doi.org/10.1002/ajoc.70175
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Poly‐Substituted Imidazo[1,2‐ a ]Pyridines via a Double Annulation Strategy

M. JUNG, Ikyon Kim, Dohui Ku, Sunhee Lee et al.
Asian Journal of Organic Chemistry
Synthesis and Reactivity of Heterocycles
article

Synthesis of Poly‐Substituted Imidazo[1,2‐ a ]Pyridines via a Double Annulation Strategy

M. JUNG, Ikyon Kim, Dohui Ku, Sunhee Lee, D.‐H. KANG
article en

Abstract

Abstract A highly efficient domino process consisting of conjugate substitution, nucleophilic addition, and cycloisomerization from the reaction of enaminonitrile with propargylamine allowed for a successive double ring closure to afford a densely functionalized imidazo[1,2‐ a ]pyridine through formation of three C─N bonds.

Asian Journal of Organic ChemistryVol. 14(11)
Yonsei University (KR)
National Research Foundation of Korea
Openalex Percentile: Top 83%
Synthesis and Reactivity of Heterocycles
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