Journal of the Chemical Society. Chemical communications p. 1069 - 1071 (1985)
Update date:2022-08-10
Topics:
Fukuzumi, Shunichi
Ishikawa, Masashi
Tanaka, Toshio
The electronic substituent effects on the rates of acid catalysed reduction of aromatic aldehydes by an acid-stable NADH model compound (N-methylacridan) are shown to be very small, compatible with those observed for liver alcohol dehydrogenase catalysed reduction of aromatic aldehydes by NADH.
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