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Mechanochemical synthesis of antifungal bis(benzoxaboroles)†
Krzysztof M. Borys,Dorota Wieczorek,Magdalena Tarkowska,Agnieszka Jankowska,Jacek Lipok,Agnieszka Adamczyk-Woźniak
RSC Advances Pub Date : 10/07/2020 00:00:00 , DOI:10.1039/D0RA07767D
Abstract

Several piperazine bis(benzoxaboroles) have been obtained both in solution as well as in the solid state. The environmentally friendly mechanochemical approach – hitherto not applied for the preparation of benzoxaboroles – was particularly beneficial in the case of two products afforded in low yields in solution. The in vitro studies showed high potential of the studied bis(fluorobenzoxaboroles) as antifungal agents, highlighting also the influence of the fluorine substituent position on their microbiological activity. The highest activity against A. niger, A. terreus, P. ochrochloron, C. tenuis and C. albicans was displayed by the analogue of the known benzoxaborole antifungal drug Kerydin® (Tavaborole).

Graphical abstract: Mechanochemical synthesis of antifungal bis(benzoxaboroles)
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