Silver-Catalyzed Cascade Approach to Access Fused Pyrazolo-naphthyridine and -isoquinoline Backbones and Investigation of Their Photophysical Properties

We describe a novel approach for synthesizing diverse fused heterocyclic compounds by utilizing a sequential silver(I) catalyzed reaction between readily obtainable <i>N</i>-amidonaphthyridin ylide and dialkyl acetylenedicarboxylates. This method provides an efficient approach for the selective synthesis of tetracyclic ring-fused 1,6-naphthyridine and isoquinoline derivatives, offering exceptional structural diversity. In addition, the title compounds constitute an interesting class of luminophores with tunable emission solvatochromicity.

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Journal
ACS Omega
Published
2025-04-04
DOI
https://doi.org/10.1021/acsomega.4c11109
Citations
1
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.94

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article

Silver-Catalyzed Cascade Approach to Access Fused Pyrazolo-naphthyridine and -isoquinoline Backbones and Investigation of Their Photophysical Properties

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1 citations
ACS Omega
Chemical synthesis and alkaloids
0.94
article

Silver-Catalyzed Cascade Approach to Access Fused Pyrazolo-naphthyridine and -isoquinoline Backbones and Investigation of Their Photophysical Properties

Saeed Balalaie, Kamran Amiri, Hamid Reza Bijanzadeh, Mohammad Rezaei-Gohar, Frank Röminger, Fatemeh Abdiyan Mobarakeh
article en
1 citations

Abstract

We describe a novel approach for synthesizing diverse fused heterocyclic compounds by utilizing a sequential silver(I) catalyzed reaction between readily obtainable <i>N</i>-amidonaphthyridin ylide and dialkyl acetylenedicarboxylates. This method provides an efficient approach for the selective synthesis of tetracyclic ring-fused 1,6-naphthyridine and isoquinoline derivatives, offering exceptional structural diversity. In addition, the title compounds constitute an interesting class of luminophores with tunable emission solvatochromicity.

ACS OmegaVol. 10(14)
Tarbiat Modares University (IR), Heidelberg University (DE), K. N. Toosi University of Technology (IR)
Alexander von Humboldt-Stiftung, Iran National Science Foundation
Openalex Percentile: Top 27%
Chemical synthesis and alkaloids
0.94
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