1997
DOI: 10.1016/s1010-6030(97)00245-1
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The mechanism of oxidation of NADH analogues 4. Photooxidation of N-acetyl-substituted 1,4-dihydropyridine in the presence of quinones

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Cited by 9 publications
(4 citation statements)
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“…This is also corroborated by the polarization effects in the aromatic region (Fig. 2) detected for the 4′,6′‐H, which is in agreement with the HFI distribution in this radical ( 17 ).…”
Section: Discussionsupporting
confidence: 85%
“…This is also corroborated by the polarization effects in the aromatic region (Fig. 2) detected for the 4′,6′‐H, which is in agreement with the HFI distribution in this radical ( 17 ).…”
Section: Discussionsupporting
confidence: 85%
“…83 Photoinduced oxidations of Hantzsch 1,4-dihydropyridines have been performed through SET processes with CCl 4 , 103 and quinones. 104 Electrochemical oxidation of 4-(pyridinium-3-yl)-1,4-dihydropyridines and 1,2-dihydropyridines (arising from [3 ϩ 2] cycloadditions) affords the aromatized compounds; occasional cyclizations at the 4-substituent to yield indolizines have also been reported. 105 Remarkable oxidations of enantiomerically pure Hantzsch-type dihydropyridines have allowed the enantioselective synthesis of atropoisomeric γ-arylpyridines; in this way NOBF 4 reacts with dihydropyridine (S )-59 to yield pyridine (R)-60 (95% ee), whereas MnO 2 or TEMPO ϩ -BF 4…”
Section: Oxidationmentioning
confidence: 99%
“…The reaction was initiated by the addition of the metal salt into the sample. Dihydropyridines are quite sensitive to external influences, such as light [ 76 ], therefore samples were incubated at a temperature of 278 K and in the absence of light in order to minimize the effect of DHP autoxidation. The 1 H-NMR spectra were also recorded using a Bruker AVHD-500 spectrometer (500 MHz).…”
Section: Methodsmentioning
confidence: 99%