Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine

Shunichi Fukuzumi; Makoto Chiba; Toshio Tanaka

doi:10.1039/C39890000941

Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine

Shunichi Fukuzumi
, Makoto Chiba
, Toshio Tanaka

Department of Chemistry & Nanoscience

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound proceeds efficiently under mild conditions in the presence of perchloric acid in acetonitrile.

Original language	English
Pages (from-to)	941-943
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	14
DOIs	https://doi.org/10.1039/C39890000941
State	Published - 1989

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@article{2f630e1ee1b542008117da69a92d46a0,

title = "Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine",

abstract = "Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound proceeds efficiently under mild conditions in the presence of perchloric acid in acetonitrile.",

author = "Shunichi Fukuzumi and Makoto Chiba and Toshio Tanaka",

year = "1989",

doi = "10.1039/C39890000941",

language = "English",

pages = "941--943",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "Chemical Society",

number = "14",

}

Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine. / Fukuzumi, Shunichi; Chiba, Makoto; Tanaka, Toshio.
In: Journal of the Chemical Society, Chemical Communications, No. 14, 1989, p. 941-943.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine

AU - Fukuzumi, Shunichi

AU - Chiba, Makoto

AU - Tanaka, Toshio

PY - 1989

Y1 - 1989

N2 - Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound proceeds efficiently under mild conditions in the presence of perchloric acid in acetonitrile.

AB - Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound proceeds efficiently under mild conditions in the presence of perchloric acid in acetonitrile.

UR - https://www.scopus.com/pages/publications/37049085777

U2 - 10.1039/C39890000941

DO - 10.1039/C39890000941

M3 - Article

AN - SCOPUS:37049085777

SN - 0022-4936

SP - 941

EP - 943

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 14

ER -

Acid-catalysed multi-electron reduction of nitrobenzene derivatives by a dihydronicotinamide adenine dinucleotide (NADH) model compound, 9,10-dihydro-10-methylacridine

Abstract

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