3-Formylpyrazolo[1,5-a]pyrazine-4-carboxylates as new bielectrophilic reagents in the cascade synthesis of polyazaacenaphthylene and polyazaacetanthrylene derivatives

It has been shown that 3-formylpyrazolo[1,5-a]pyrazine-4-carboxylates obtained by the selective formylation of pyrazolo[1,5-a]pyrazine-4-carboxylates react with 1,2-ethanediamine or 1,3-propanediamine in methanol at room temperature to give pentaazacyclopenta[d]acenaphthalenes or pentaazaaceanthrylenes.

Authors

Publication Details

Journal
Current Chemistry Letters
Published
2025-01-01
DOI
https://doi.org/10.5267/j.ccl.2025.5.002
Citations
1
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.94
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article

3-Formylpyrazolo[1,5-a]pyrazine-4-carboxylates as new bielectrophilic reagents in the cascade synthesis of polyazaacenaphthylene and polyazaacetanthrylene derivatives

Maryna Stasevych, Svitlana V. Shishkina, N. M. Tsyzoryk, Khrystyna I. Loza et al.
1 citations
Current Chemistry Letters
Synthesis and Biological Evaluation
0.94
article

3-Formylpyrazolo[1,5-a]pyrazine-4-carboxylates as new bielectrophilic reagents in the cascade synthesis of polyazaacenaphthylene and polyazaacetanthrylene derivatives

Maryna Stasevych, Svitlana V. Shishkina, N. M. Tsyzoryk, Khrystyna I. Loza, M. V. Vovk, Andriy V. Bol’but
article en
1 citations

Abstract

It has been shown that 3-formylpyrazolo[1,5-a]pyrazine-4-carboxylates obtained by the selective formylation of pyrazolo[1,5-a]pyrazine-4-carboxylates react with 1,2-ethanediamine or 1,3-propanediamine in methanol at room temperature to give pentaazacyclopenta[d]acenaphthalenes or pentaazaaceanthrylenes.

Current Chemistry LettersVol. 14(3)
Openalex Percentile: Top 25%
Synthesis and Biological Evaluation
0.94
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