Synthesis and structural elucidation of novel antifungal N-(fluorophenyl)piperazinyl benzoxaboroles and their analogues

被引:15
|
作者
Borys, Krzysztof M. [1 ]
Matuszewska, Alicja [1 ]
Wieczorek, Dorota [2 ]
Kopczynska, Karolina [1 ]
Lipok, Jacek [2 ]
Madura, Izabela D. [1 ]
Adamczyk-Wozniak, Agnieszka [1 ]
机构
[1] Warsaw Univ Technol, Fac Chem, Noakowskiego 3, PL-00664 Warsaw, Poland
[2] Opole Univ, Fac Chem, Oleska 48, PL-45052 Opole, Poland
关键词
Benzoxaborole; Phenylboronic acid; Piperazine; Fluorophenyl; Organoboron; Antifungal activity; PIPERAZINE DERIVATIVES; BORONIC ACIDS; 2-FORMYLPHENYLBORONIC ACID; BIOLOGICAL-ACTIVITY; DESIGN; REACTIVITY; AMINES; DRUGS;
D O I
10.1016/j.molstruc.2019.01.018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Series of novel N-(fluorophenyl)piperazine derivatives of phenylboronic compounds including benzoxaboroles, phenylboronic acids and phenylboronic methyl monoester have been obtained by facile synthetic methods starting from 2-formylphenylboronic acid. Molecular and crystal structures of those novel derivatives have been investigated by single crystal X-ray diffraction method. The Bond Valence Vector Model was used to describe strains in the boron coordination sphere. Microbiological activity of novel benzoxaboroles as well as their corresponding acid analogues against: A. niger, A. terreus, P. ochrochloron, C. tenuis and F. dimerum has been evaluated. The presence of heterocyclic benzoxaborole ring has been shown to be crucial for the studied activity. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:587 / 598
页数:12
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