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72 results for “Pyrrole”
Figure 1 from: Mateev E, Irfan A, Mateeva A, Kondeva-Burdina M, Georgieva M, Zlatkov A (2024) In silico and in vitro screening of pyrrole-based Hydrazide-Hydrazones as novel acetylcholinesterase inhibitors. Pharmacia 71: 1-7. https://doi.org/10.3897/pharmacia.71.e114120
Figure 1 Workflow for identifying novel pyrrole-based acetylcholinesterase inhibitors.
Scheme 4 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 4 Microwave irradiated condensation of diketone with primary amine.
Scheme 1 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 1 General Paal-Knorr synthesis of pyrroles.
Figure 4 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Figure 4 Chemical reactions of the pyrrole.
Scheme 22 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 22 Synthesis of N-substituted pyrrole derivatives with nanocatalysts or MW.
Scheme 11 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 11 Microwave-Assisted Sila-Stetter/Paal-Knorr Reaction
Scheme 18 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 18 Clauson-Kaas synthesis of pyrroles catalyzed by [hmim][HSO4].
Figure 1 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Figure 1 Electromagnetic spectrum.
Scheme 10 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 10 Nano-organocatalyst promoted Paal-Knorr reaction.
Scheme 14 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 14 Paal-Knorr MW synthesis in the presence of alkaline salts as catalysts.
Scheme 25 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 25 MW assisted synthesis of 1,2-disubstituted pyrroles on the surface of silica gel.
Scheme 17 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 17 Synthesis of 2-pyrrolin-5-ones by Hantzsch-type reaction.
Scheme 24 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 24 MW irradiated synthesis of functionalized pyrroles using UO2(NO3).6H2O as a catalyst.
Scheme 7 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 7 MW synthesis of pyrroles from diketons and acetic acid.
Figure 2 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Figure 2 Major advantages of MW assisted synthesis.
Scheme 16 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 16 Solvent-free MW synthesis of pyrroles with organocatalyst.
Scheme 21 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 21 Solvent-free synthesis of novel sulfonylpyrroles by MW heating.
Scheme 13 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 13 Synthesis of Tetra-substituted Pyrrole Amide Library.
Scheme 19 from: Mateev E, Irfan A, Mateeva A, Georgieva M, Zlatkov A (2024) Microwave-assisted organic synthesis of pyrroles (Review). Pharmacia 71: 1-10. https://doi.org/10.3897/pharmacia.71.e119866
Scheme 19 MW synthesis of pyrrole by reacting furan-2,5-dione with 3-phenylenediamine.
Figure 6 from: Tzankova D, Peikova L, Vladimirova S, Georgieva M (2019) Development and validation of RP-HPLC method for stability evaluation of model hydrazone, containing a pyrrole ring. Pharmacia 66(3): 127-134. https://doi.org/10.3897/pharmacia.66.e47035
Figure 6 Linearity of the developed RP-HPLC D_5d stability indicating method.
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