Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridine with sodium periodate is reported. The Mn(III)-salophen/NaIO4 catalytic system converts 1,4-dihydropyridines to their corresponding pyridine derivatives at room temperature in a 1:1, CH3CN/H2O mixture. The ability of various Schiff base complexes in the oxidation of 1,4-dihydropyridine was also investigated.
Room Temperature Catalytic Aromatization of Hantzsch 1,4-Dihydropyridines by Sodium Nitrite in the Presence of Acidic Silica Gel
作者:Mohammed M. Hashemi、Hossein Ghafuri、Zahed Karimi-Jaberi
DOI:10.1007/s00706-005-0425-5
日期:2006.2
Various alkyl, aryl, and heterocyclic Hantzsch 1,4-dihydropyridines were converted to the corresponding pyridines in excellent yields and short times using sodium nitrite in the presence of a catalytic amount of acidic silica gel at roomtemperature.
Biomimetic oxidation of Hantzsch 1,4-dihydropyridines with tetra-n-butylammonium periodate catalyzed by tetraphenylporphyrinatomanganese(III) chloride [Mn(TPP)Cl]
Efficient oxidation of Hantzsch 1,4-dihydropyridines to their corresponding pyridine derivatives with (BU4N)IO4 catalyzed by tetraphenylporphyrinatomanganese(III) chloride [Mn(TPP)Cl] is reported. This catalytic system shows high efficiency in the oxidation of 1,4-dihydropyridines at room temperature in the presence of imidazole. (c) 2005 Published by Elsevier Ltd.