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首页> 外文期刊>Comptes Rendus Chimie >Solvent-free synthesis of novel unsymmetric chenodeoxycholic acid bis thiocarbazone derivatives promoted by microwave irradiation and evaluation of their antibacterial activity
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Solvent-free synthesis of novel unsymmetric chenodeoxycholic acid bis thiocarbazone derivatives promoted by microwave irradiation and evaluation of their antibacterial activity

机译:微波辐射促进新的不对称鹅去氧胆酸双硫代咔唑衍生物的无溶剂合成及其抗菌活性的评价

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摘要

Eleven new non-symmetric chenodeoxycholic acid bis thiocarbazones were efficiently synthesized via the condensation of steroidal diketones (methyl (5β)-3,7-dioxocholan-24-oate) and substituted benzaldehyde thiocarbohydrazones by means of microwave irradiation. Compared with the conventional heating method, the yields were increased from 31-58% to 80-89% and the reaction times were reduced from 420-520 min to 5.0-7.5 min. The structures of these novel compounds were characterized by spectral data and elemental analysis. Four compounds (7a, 7c, 7f and 7g) possess excellent activity against Bacillus subtilis and Staphylococcus aureus.
机译:通过甾体二酮((5β)-3,7-dioxocholan-24-oate(methyl(5β)-3,7-dioxocholan-24-oate))和取代的苯甲醛硫代碳氢hydr酮的缩合反应,有效合成了十一种新的不对称鹅去氧胆酸双硫代碳唑酮。与常规加热方法相比,产率从31-58%增加到80-89%,反应时间从420-520分钟减少到5.0-7.5分钟。这些新型化合物的结构通过光谱数据和元素分析进行​​了表征。四种化合物(7a,7c,7f和7g)对枯草芽孢杆菌和金黄色葡萄球菌具有优异的活性。

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