192518-51-7Relevant articles and documents
Syntheses and redox behavior of novel cyclic hosts having multiple redox centers of NAD+ analogue
Kuroda, Yasuhisa,Seshimo, Hidenori,Kondo, Toshio,Shiba, Masana,Ogoshi, Hisanobu
, p. 3939 - 3942 (1997)
A new series of cyclophanes having 3,5-dicarbanoylpyridinium moieties were synthesized by the stepwise reactions starting from half protected compounds. The one-electron reduction potentials of these new cyclophane type NAD+ analogues are determined by the cyclic voltammetric method. The results indicate that the reduction potentials are primarily regulated by the through-bond mechanism.
