Synthesis of 3,4,5-Trisubstituted 1H-Pyrazoles Based on 2,3-Dienoates with a Pyrrolidinedione Fragment

A simple and convenient method has been developed for the regioselective synthesis of new 3,4,5-trisubstituted pyrazole derivatives via 1,3-dipolar cycloaddition of diazo ketone to 2,3-dienoates obtained from the condensation products of dicarboxylic acid anhydrides and 3-aminobutanoic aicd.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1134/s1070428024603005
Citations
1
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.81
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article

Synthesis of 3,4,5-Trisubstituted 1H-Pyrazoles Based on 2,3-Dienoates with a Pyrrolidinedione Fragment

И. М. Сахаутдинов, G. M. Gindullina
1 citations
Russian Journal of Organic Chemistry
Chemical Synthesis and Analysis
0.81
article

Synthesis of 3,4,5-Trisubstituted 1H-Pyrazoles Based on 2,3-Dienoates with a Pyrrolidinedione Fragment

И. М. Сахаутдинов, G. M. Gindullina
article en
1 citations

Abstract

A simple and convenient method has been developed for the regioselective synthesis of new 3,4,5-trisubstituted pyrazole derivatives via 1,3-dipolar cycloaddition of diazo ketone to 2,3-dienoates obtained from the condensation products of dicarboxylic acid anhydrides and 3-aminobutanoic aicd.

Russian Journal of Organic ChemistryVol. 61(1)
Ufa Institute of Chemistry (RU)
Openalex Percentile: Top 30%
Chemical Synthesis and Analysis
0.81
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Synthesis of 3,4,5-Trisubstituted 1H-Pyrazoles Based on 2,3-Dienoates with a Pyrrolidinedione Fragment — И. М. Сахаутдинов, G. M. Gindullina · Russian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS