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Mendeleev Communications, 2021, Volume 31, Issue 5, Pages 573–583
DOI: https://doi.org/10.1016/j.mencom.2021.09.001
(Mi mendc994)
 

This article is cited in 9 scientific papers (total in 9 papers)

Focus Article

Conjugated pyrrole/aminoenone and pyrrole/aminoacrylonitrile ensembles: new motives in heterocyclic chemistry

L. N. Sobenina, E. F. Sagitova, O. V. Petrova, B. A. Trofimov

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
Full-text PDF (540 kB) Citations (9)
Abstract: Methods for the preparation of two highly flexible synthetic building blocks, namely pyrrole/aminoenone and pyrrole/aminoacrylonitrile ensembles, on the basis of available starting materials such as 2-acylethynylpyrroles or pyrrole-2-carbodithioates, are summarized. The presence of several reactive centers in their molecules (pyrrole ring, enamine and carbonyl or nitrile moieties) ensures their multiple reactivity and application as versatile intermediates in the synthesis of heterocyclic ensembles such as pyrrolyl pyridines, bipyrroles, pyrrolyl-isoxazoles and condensed compounds, such as pyrrolo[3,2-a]pyrazines, pyrrolizines, which have high potential for use in medical chemistry and materials science.
Keywords: pyrrole, acylethynylpyrrole, aminoenone, aminoacrylonitrile, pyridine, pyrrolo[1,2-a]pyrazine, pyrrolizine, bipyrrole, pyrrolyl-isoxazole, cyclization.
Bibliographic databases:
Document Type: Article
Language: English


Citation: L. N. Sobenina, E. F. Sagitova, O. V. Petrova, B. A. Trofimov, “Conjugated pyrrole/aminoenone and pyrrole/aminoacrylonitrile ensembles: new motives in heterocyclic chemistry”, Mendeleev Commun., 31:5 (2021), 573–583
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  • This publication is cited in the following 9 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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