Microwave-assisted Synthesis of Nـ alkyl 2ـ ketomethyl quinoline Derivatives Under Solvent-free Conditions
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Abstract:
A series of Nـ alkyl 2ـ ketomethylquinoline derivatives were synthesis by reaction of benzoyl chloride derivatives with Nـ methyl quinaldine iodide in the presence of triethyl amine under microwave irradiation. Enaminone form of the product study by spectroscopy method. The result revealed the Nـ alkyl 2ـ ketomethylquinoline the fixed enaminone tautomer.
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Microwave-assisted preparation of Nـ alkyl 2ـ ketomethyl quinolines on Solvent-free Conditions
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Microwave-accelerated preparation of Nـ alkyl 2ـ ketomethyl quinoline Derivatives
A series of Nـ alkyl 2ـ ketomethylquinoline derivatives were synthesis by reaction of benzoyl chloride derivatives with Nـ methyl quinaldine iodide in the presence of triethyl amine under microwave irradiation. Enaminone form of the product study by spectroscopy method. The result revealed the Nـ alkyl 2ـ ketomethylquinoline the fixed enaminone tautomer.
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phthalocyanine complexes of cu, co, ni, fe, zn, pd, pt and ru have been synthesized from reaction between phthalonitrile and proper metal salts upon exposure to microwave irradiation under solvent-free conditions and considerably reduced reaction times.
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Este trabalho descreve a síntese de 4,5-diidro-1H-pirazóis pela reação de ciclocondensação de hidrazinas [NH 2 NH-R, onde R = CO 2 Me, Ph, CH 2 CH 2 OH] com 4-alcóxi-1,1,1-trifluor-3-alquen2-onas [CF 3 C(O)CH=C(R)OR, onde R/R = Et/H, Me/Me and Me/Ph] sob irradiação de microondas utilizando um equipamento de micro-ondas para síntese e em condição livre de solvente. Algumas reações foram realizad...
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Journal title
volume 1 issue 2
pages 35- 42
publication date 2011-05-01
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