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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Doi:10.1007/BF00904135
()Doi:10.1021/ja3054139
(2012)Doi:10.1021/acs.joc.8b00913
(2018)Doi:10.1016/S0040-4039(00)93627-X
(1980)Doi:10.1021/jo00024a035
(1991)Doi:10.1016/j.molstruc.2016.07.077
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