clisen Schmidt-Suzuki交叉偶联法合成(E)-(4-(芳基)苯基)(3-(2-(1-苯基-3-(噻吩-2-基)-1吡唑-4-基)乙烯基)苯并呋喃-2-基)甲烷及其抑菌抑菌活性

A. Dongamanti, M. Ziauddin, B. Lakshmi, M. Sarasija
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引用次数: 0

摘要

采用传统的Claisen-Schmidt和Suzuki交叉偶联反应,在常规和微波辐照条件下制备了10个新的(E)-(4-(芳基)苯基)(3-(2-(1-苯基-3-(噻吩-2-基)-1 H -吡唑-4-基)乙烯基)苯并呋喃-2-基)甲烷(7a-j)衍生物。根据FTIR、1h NMR、13c NMR、质谱数据和元素分析确定了所有新合成化合物的结构。测定产物对不同类型细菌的体外抑菌活性。进一步通过对黑曲霉、黄曲霉和尖孢镰刀菌的抑菌作用,考察了其抑菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of (E)-(4-(Aryl)phenyl)(3-(2-(1-phenyl-3-(thiophen-2-yl)-1Hpyrazol-4-yl)vinyl)benzofuran-2-yl)methanones by Claisen Schmidt-Suzuki Cross Coupling and their Antibacterial and Antifungal Activity
A series of ten novel ( E )-(4-(aryl)phenyl)(3-(2-(1-phenyl-3- (thiophen-2-yl)-1 H -pyrazol-4-yl)vinyl)benzofuran-2-yl)methanones ( 7a-j ) derivatives were prepared by traditional Claisen-Schmidt and Suzuki cross-coupling reaction under conventional and microwave irradiation conditions. The structures of all the newly synthesized compounds were established on the basis of FTIR, 1 H NMR, 13 C NMR, mass spectral data and elemental analysis. The products were assayed for their in vitro antibacterial activity against different types of bacterial strains. Further the antifungal activity was examined by inhibitory action against three fungal strains such as Aspergillus niger , Aspergillus flavus and Fusarium oxysporum .
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