Synthesis and antiviral activity of 3-cyano-2(1H)pyridine selenones

Mortikov, V. Yu.; Литвинов, В. П.; Шестопалов, А. М.; Sharanin, Yu. A.; Apenova, E. E.; Галегов, Г. А.; Abdullaev, Ikrаm; Asadullaev, T. B.; Abdullaev, Fikrat I.

doi:10.1007/bf00772121

Cited by 7 publications

(4 citation statements)

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“…Seleno-substitution products were obtained when α-haloketones reacted with seleno-nucleophiles [ 626 , 627 , 628 , 629 , 630 , 631 , 632 , 633 , 634 , 635 , 636 ]. For example, a series of selenophenopyridines 323 , with antiviral activity, could be prepared via reaction of 3-cyano-2(1 H )-pyridineselenones 322 with α-haloketones ( Scheme 93 ) [ 637 , 638 ].…”

Section: Miscellaneous Reactions Of α-Haloketonesmentioning

confidence: 99%

The Chemistry of α-Haloketones and Their Utility in Heterocyclic Synthesis

2003

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Section: Miscellaneous Reactions Of α-Haloketonesmentioning

confidence: 99%

The Chemistry of α-Haloketones and Their Utility in Heterocyclic Synthesis

2003

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“…After 7-8 days, the green complex precipitate formed was separated, washed in ethanol The structure of the obtained compound was analyzed by X-ray and it was determined that it has the following structure (Figure 1). [11][12][13][14][15][16][17].…”

Section: Synthesis Methodologymentioning

confidence: 99%

SYNTHESIS AND ANALYSIS OF COORDINATION COMPOUNDS OF NICKEL(II) ACETATE WITH MONOETHANOLAMINE AND p-NITROBENZOIC ACID

Ibragimov¹

2022

AChJ

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This article clarifies the synthesis of a complex combination of p-nitrobenzoic acid with Ni2+ from aromatic carbonic acid derivatives. Moreover, factors influencing the synthesis of the complex compound under room conditions were identified. In particular, the time dependence of the reaction, the effect of temperature, the concentration dependence were studied in practice. The synthesized complex was studied using IR-Fourier spectrometry, elemental analysis, mass spectrometry, TG-DSK and X-ray structural analysis, its chemical structure was determined, and this new complex was proved to be thermally and chemically stable

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“…Selenosubstitution products were obtained when α-haloketones reacted with selenonucleophiles [626][627][628][629][630][631][632][633][634][635][636]. For example, a series of selenophenopyridines 323, with antiviral activity, could be prepared via reaction of 3-cyano-2(1H)-pyridineselenones 322 with α-haloketones (Scheme 93) [637,638].…”

Section: F Selenationmentioning

confidence: 99%