aromatization of 1,4-dihydropyridines with free radical reagents

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چکیده

oxidation of different types of 1,4-dihydropyridines with diphenylpicrylhydrazyl (dpp) and benzoyl peroxide (bz2o2) as free radical oxidizing agents to pyridine derivatives is reported and a mechanism for this oxidation is also proposed.

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AROMATIZATION OF 1,4-DIHYDROPYRIDINES WITH FREE RADICAL REAGENTS

Oxidation of different types of 1,4-dihydropyridines with diphenylpicrylhydrazyl (DPP) and benzoyl peroxide (Bz2O2) as free radical oxidizing agents to pyridine derivatives is reported and a mechanism for this oxidation is also proposed.

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AROMATIZATION OF HANTZSCH 1,4- DIHYDROPYRIDINES WITH ZINC CHLOROCHROMATE NONAHYDRATE

Hantzsch 1 ,4- dihy&opyridines are rapidly oxidized to the corresponding pyridine derivatives using zinc chlorochromate nonahydrate [Zn(C1CrO ) .9H O] in dichloromethane at room temperature. In addition to aromatization, no loss of the 4- substituent is observed

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aromatization of hantzsch 1,4- dihydropyridines with zinc chlorochromate nonahydrate

hantzsch 1 ,4- dihy&opyridines; are rapidly oxidized to the corresponding pyridine derivatives using zinc chlorochromate nonahydrate [zn(c1cro ) .9h o] in dichloromethane at room temperature. in addition to aromatization, no loss of the 4- substituent is observed

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Green Synthesis and Characterization of Bi2O3 Nanorods as Catalyst for Aromatization of 1,4-Dihydropyridines

Bismuth oxide (Bi2O3) nanorods was prepared via one pot sol-gel method using Bi(NO3)3.5H2O and starch (as template) in water under hydrothermal condition followed by calcination at 320˚C within 3 h. The resultant solid product was characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), thermogravimetry (TGA), and FTIR techniques. Based on the obtained results, the formatio...

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Synthesis and Aromatization of Hantzsch 1 , 4 - Dihydropyridines under Microwave Irradiation . An Overview

Domestic microwave ovens as well as laboratory reactors have been successfully employed to prepare dialkyl 1,4-dihydropyridine-3,5-dicarboxylates and to induce the synthesis of the corresponding aromatic derivatives. In that latter particular case, unexpected results have been reported.

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Oxidative aromatization of some 1,4-dihydropyridines by aqueous hydrogen peroxide in ethanol

Some 3, 5-diacyl or 3,5-diester 1,4-dihydropyridines were oxidized to the corresponding pyridine derivatives using hydrogen peroxide in aqueous ethanol in the presence of potassium bromide and acetic acid as the catalysts. The reaction was carried out in ethanol and products were isolated in high to excellent yields. However, oxidation of 3,5-diacetyl 1,4-dihydropyridines is slower than 3,5-die...

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عنوان ژورنال:
journal of sciences islamic republic of iran

جلد ۱۲، شماره ۲، صفحات ۰-۰

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