Cu(acac)2-Catalyzed A3-(Aldehyde-amine-alkyne) Coupling Reaction for the Synthesis of a Wide Range of Propargylamines and Entry to Imidazo[1,2-a]pyridines

Abstract Cu(acac)2-catalyzed A3-coupling reactions involving an amine, an aldehyde, and a terminal alkyne were explored for the efficient synthesis of a broad range of propargylamines and imidazo[1,2-a]pyridines. This method demonstrates a wide substrate scope and delivers the desired products in good yields under mild reaction conditions. The protocol offers a straightforward and practical approach to accessing these valuable scaffolds, making it attractive for further synthetic applications.

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Publication Details

Journal
Synthesis
Published
2025-09-04
DOI
https://doi.org/10.1055/a-2695-8185
Primary Topic
Catalytic Alkyne Reactions
Type
article
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article

Cu(acac)2-Catalyzed A3-(Aldehyde-amine-alkyne) Coupling Reaction for the Synthesis of a Wide Range of Propargylamines and Entry to Imidazo[1,2-a]pyridines

Ujjal Kanti Roy, Upendra Pappula, Venkata Prasad Kalyana
Synthesis
Catalytic Alkyne Reactions
article

Cu(acac)2-Catalyzed A3-(Aldehyde-amine-alkyne) Coupling Reaction for the Synthesis of a Wide Range of Propargylamines and Entry to Imidazo[1,2-a]pyridines

Ujjal Kanti Roy, Upendra Pappula, Venkata Prasad Kalyana
article en

Abstract

Abstract Cu(acac)2-catalyzed A3-coupling reactions involving an amine, an aldehyde, and a terminal alkyne were explored for the efficient synthesis of a broad range of propargylamines and imidazo[1,2-a]pyridines. This method demonstrates a wide substrate scope and delivers the desired products in good yields under mild reaction conditions. The protocol offers a straightforward and practical approach to accessing these valuable scaffolds, making it attractive for further synthetic applications.

SynthesisVol. 57(23)
Kazi Nazrul University (IN)
Openalex Percentile: Top 82%
Catalytic Alkyne Reactions
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