Chiral methylbenzylammonium salts of aryldithiophosphonic acids containing glucofuranose,allofuranose, and galactopyranose diacetonide scaffolds |
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Authors: | Ilyas S. Nizamov Georgiy G. Shumatbaev Ilnar D. Nizamov Yevgeniy N. Nikitin Timur G. Belov Marina P. Shulaeva |
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Affiliation: | 1. A.M. Butlerov Chemical Institute, Kazan Federal University, Kazan, Russia;2. A.E. Arbuzov Institute of Organic and Physical Chemistry, Federal Research Center, Kazan Scientific Center, Russian Academy of Sciences, Kazan, Russia isnizamov@mail.ruhttps://orcid.org/0000-0002-2058-773X;4. A.M. Butlerov Chemical Institute, Kazan Federal University, Kazan, Russia https://orcid.org/0000-0003-1199-3178;5. A.M. Butlerov Chemical Institute, Kazan Federal University, Kazan, Russia https://orcid.org/0000-0002-8243-3533;6. Federal State Budgetary Institution of Science Federal Research Center, Kazan Scientific Center of Russian Academy of Sciences, Kazan, Russia;7. A.M. Butlerov Chemical Institute, Kazan Federal University, Kazan, Russia https://orcid.org/0000-0002-1657-2850;8. Department of Microbiology, Kazan State Medical Academy, Kazan, Russia |
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Abstract: | Abstract New chiral methylbenzylammonium salts of aryldithiophosphonic acids containing glucofuranose, allofuranose, and galactopyranose diacetonide substituents were obtained using (S)-(–)-α-methylbenzylamine, (R)-(+)-α-methylbenzylamine, and (R,S)-(±)-α-methylbenzylamine. Salts obtained possess antimicrobial activity. |
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Keywords: | Carbohydrates dithiophosphonic acids methylbenzylamines antimicrobial activity |
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