104785-61-7Relevant academic research and scientific papers
Stereospecific Electrochemical Oxidation of NAD(P)H Analogs Mediated by Radical Cation of Anilines
Okamura, Mutsuo,Kashiwagi, Takeshi,Mikata, Yuji,Yamazaki, Norimasa,Ohno, Atsuyoshi
, p. 1247 - 1250 (1992)
Net hydrogen-atom (H) transfer was observed in electrochemical oxidation of NAD(P)H analogs in the presence of aniline or its derivatives.The reaction mechanism is discussed on the basis of stereospecifities.
NAD(P)H-NAD(P)+ Models. 73. Structure-Stereochemistry Relationship in the Reaction of NAD Analog
Ohno, Atsuyoshi,Mikata, Yuji,Goto, Mutsuo,Kashiwagi, Takeshi,Tanaka, Takanori,Sawada, Masami
, p. 81 - 86 (2007/10/02)
Four different NAD(P)H analogs have been oxidized by various substituted and unsubstituted 1,4-benzoquinones in the presence or absence of magnesium ion.The stereospecificity of the reaction depends not only on the reactivity of quinone but also on that of the analogs as well as on the presence or absence of magnesium ion.The results are discussed from the viewpoint of reaction mechanism for the transfer of a (net) hydride ion.
