New Polyfunctional N-Terpenyl-4-aminobenzenesulfonamides

By the reaction of polyfunctional pinane and bornane amines, including fluorine-containing ones, with N-acetylsulfanyl chloride and subsequent removal of the terminal acyl group with thionyl chloride, new optically active sulfonamides were obtained in yields of 38–98%. Data from X-ray diffraction analysis of fluorine-containing sulfonamide with bornane structure are presented. It was shown that the resulting compounds exhibit weak antimicrobial activity.

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Publication Details

Journal
Журнал Общей Химии
Published
2024-08-13
DOI
https://doi.org/10.31857/s0044460x24030104
Citations
1
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.25
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article

New Polyfunctional N-Terpenyl-4-aminobenzenesulfonamides

Д. В. Судариков, O. M. Lezina, С. А. Рубцова, P. A. Petrova et al.
1 citations
Журнал Общей Химии
Synthesis and biological activity
0.25
article

New Polyfunctional N-Terpenyl-4-aminobenzenesulfonamides

Д. В. Судариков, O. M. Lezina, С. А. Рубцова, P. A. Petrova, O. N. Grebyonkina, P. V. Gribkov, R. V. Rumyantсev
article en
1 citations

Abstract

By the reaction of polyfunctional pinane and bornane amines, including fluorine-containing ones, with N-acetylsulfanyl chloride and subsequent removal of the terminal acyl group with thionyl chloride, new optically active sulfonamides were obtained in yields of 38–98%. Data from X-ray diffraction analysis of fluorine-containing sulfonamide with bornane structure are presented. It was shown that the resulting compounds exhibit weak antimicrobial activity.

Журнал Общей ХимииVol. 94(3)
Russian Academy of Sciences (RU), Institute of Biology of Komi Scientific Centre (RU)
Clean water and sanitation
Openalex Percentile: Top 49%
Synthesis and biological activity
0.25
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