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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Multicomponent reaction of aldehydes, amines and oxalacetate analogues leading to biologically attractive pyrrole derivatives

Thumbnail
Autor
Manta S., Kollatos N., Mitsos C., Chatzieffraimidi G.-A., Papanastasiou I., Gallos J.K., Komiotis D.
Fecha
2020
Language
en
DOI
10.2174/1389557520666200103123114
Materia
1 (4 aminosulfonylphenyl) 5 aryl 4 acyl 3 hydroxy 3 pyrrolin2 one derivative
1 (4 antipyryl) 5 aryl 4 aroyl 3 pyrrolin 2 one derivative
1 methyl 5 aryltetrahydropyrrole 2,3 dione derivative
1,5 diaryl 4 ethoxycarbonyltetrahydropyrrole 2,3 dione derivative
1,5 diaryl 4 heteroyl 3 hydroxy 3 pyrrolin 2 one derivative
1,5 diaryltetrahydropyrrole 2,3 dione derivative
2,3 dioxo 5 (4 halophenyl)pyrrolidine derivative
2,3 dioxo 5 (hetero)arylpyrrolidine derivative
3 hydroxy 1,5 dihydro 2h pyrrol 2 one derivative
3 hydroxy 3 pyrrolin 2 one derivative
5 aryl 4 acyl (heteroyl) 3 hydroxy 1 (3 ethoxypropyl) 3 pyrrolin 2 one derivative
5 aryl 4 acyl 1 (n,n dimethylaminoethyl) 3 hydroxy 3 pyrrolin 2 one derivative
5 aryl 4 acyl 3 hydroxy 1 (2 hydroxyethyl) 3 pyrrolin 2 one derivative
5 aryl 4 acyl 3 hydroxy 3 pyrrolin 2 one derivative
5 aryl 4 aroyl 3 hydroxy 1 (4 guanidylsulfonylphenyl) 3 pyrrolin 2 one derivative
5 aryl 4 aroyl l (2 diethylaminoethyl) 3 hydroxy 3 pyrrolin 2 one derivative
aldehyde derivative
amine
dihydrochromeno[2,3 c]pyrrole 3,9 dione derivative
oxaloacetic acid derivative
pyrrole derivative
pyrrolinone derivative
unclassified drug
aldehyde
amine
oxaloacetic acid
pyrrole derivative
analgesic activity
antibacterial activity
antileukemic activity
antimicrobial activity
antiviral activity
Article
biological activity
chemical reaction
drug screening
drug structure
drug synthesis
human
multicomponent reaction
nonhuman
one pot synthesis
structure activity relation
chemistry
drug development
Aldehydes
Amines
Drug Discovery
Oxaloacetic Acid
Pyrroles
Bentham Science Publishers
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Resumen
Pyrrole is a very important pharmacophoric moiety. It has been widely incorporated into the skeleton of antitumor, anti-inflammatory, antibacterial, antioxidant and antifungal active substances. Access to this key heterocycle by diverse routes is particularly attractive in terms of chemistry, and al-so from the environmental point of view. The present minireview summarizes the reported methods for the preparation of highly substituted pyrrole derivatives based on the one-pot multicomponent reaction of aldehydes, primary amines, and oxalacetate analogues as well as their biology. © 2020 Bentham Science Publishers.
URI
http://hdl.handle.net/11615/76291
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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