NAD(P)+-NAD(P)H models.: 88. Stereoselection without steric effect but controlled by electronic effect of a carbonyl group:: Syn/Anti reactivity ratio, kinetic isotope effect, and an electron-transfer complex as a reaction intermediate

1,4,6,7-Tetrahydro-1,6,11-trimethyl-5-oxo-5H-benzo[c]pyrido[2.3-e]azepin (11Me-MMPAH) and its 4-mono- and 4,4-dideuterated analogues have been oxidized with a series of p-benzoquinones. The compounds have axial chirality with respect to the orientation of the carbonyl dipole. The hydrogen (deuterium) at the 4-position has different reactivity toward oxidation: the anti (with respect to the carbonyl dipole) hydrogen is from 3 to 32 times more reactive than the corresponding syn hydrogen (deuterium). The syn/anti reactivity ratio depends on the reactivity of the quinone (stereoselection without steric effect). The initial electron-transfer process, which is associated with the weakening of the C-4-H(D) bond, results in the formation of an electron-transfer complex prior to the chemical reaction. The isotope effect affecting this equilibrium constant is the origin of the "product isotope effect", which has long been a subject of controversy. Kinetic primary and secondary isotope effects in the oxidation are also calculated.