A one pot, three component synthesis of coumarin hybrid thiosemicarbazone derivatives and their antimicrobial evolution
نویسندگان
چکیده
منابع مشابه
One-pot Three-component Synthesis of Phosphonate Derivatives
The stable phosphonate derivatives have easily synthesized by the reactions involving trialkyl(aryl) phosphites and dimethyl acetylenedicarboxylate in the presence of 4-nitrophenol and/or acid chlorides, dialkyl(aryl) phosphites and N-methylimidazole at 70 oC under solventfree conditions.
متن کاملAn Efficient Synthesis of 4H-chromene Derivatives by a One-pot, Three-component Reaction
A facile and efficient one-pot, multicomponent synthesis of 4H-chromenes is reported, through the reaction of arylglyoxalmonohydrates with 1,3-diketones and malononitrile in eTEMPthanol in the presence of L-proline as a catalyst.
متن کاملApplication of Non-Corrosive Acids in Three-Component, One-Pot Synthesis of Commercial Coumarin Dye
The efficiency of HZSM-5 Zeolite, tungestophosphoric acid (H3PW12O40) and tungestosililic acid (H4O40SiW12) were investigated in three-component, one-pot synthesis of coumarin dyes. These green and noncorrosive acids were highly efficient in synthesis of some coumarin dyes in excellent yield during concurrent formation of coumarin and benzimidazole or benzoxazole heterocycles (e.g. C. I. disper...
متن کاملOne pot three-component synthesis of imidazole derivatives using NH3/NH4Cl
Imidazole is a planar, five membered heteroaromatic molecule with pyrrole type and pyridine type annular nitrogens. Several approaches are available of imidazoles from alpha halo ketones, aminonitrile, aldehyde ect. Reactivity of imidazole and benzimidazole is referred from sets of resonance structure in which the dipolar contributors have finite importance. Imidazoles among the principal grou...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of the Association of Arab Universities for Basic and Applied Sciences
سال: 2017
ISSN: 1815-3852
DOI: 10.1016/j.jaubas.2016.04.002