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机构地区:[1]Department of Chemistry, Faculty of Science, KAU, Jeddah, Saudi Arabia
出 处:《International Journal of Organic Chemistry》2019年第1期37-46,共10页有机化学国际期刊(英文)
摘 要:Some new asymmetric thioethers 5 and 4-thiazolidinones 6 have been obtained from condensation of 5-formyl-3-(pyridin-4'-yl)-1,2,4-triazino[5,6-b] indole (3) with halogenated aromatic amines followed by addition of thiophenol and/or cycloaddition with thiolactic acids in nonpolar solvents. Structures of the products confirmed by elemental analysis and spectral measurements. The new systems obtained were evaluated as antifungal agents.Some new asymmetric thioethers 5 and 4-thiazolidinones 6 have been obtained from condensation of 5-formyl-3-(pyridin-4'-yl)-1,2,4-triazino[5,6-b] indole (3) with halogenated aromatic amines followed by addition of thiophenol and/or cycloaddition with thiolactic acids in nonpolar solvents. Structures of the products confirmed by elemental analysis and spectral measurements. The new systems obtained were evaluated as antifungal agents.
关 键 词:THIOETHERS Thiazolidnones 1 2 4-Triazino INDOLE FUNGICIDAL Cycloaddition
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