Issue 18, 2005

Hydroxyl radical generation via photoreduction of a simple pyridine N-oxide by an NADH analogue

Abstract

Photoreduction of pyridine N-oxide, which has a key structure of antitumor agents for hypoxic solid tumors, by 1-benzyl-1,4-dihydronicotinamide in deaerated aprotic media resulted in generation of hydroxyl radical, leading to the oxidation of salicylic acid to 2,3- and 2,5-dihydroxybenzoic acids, and catechol.

Graphical abstract: Hydroxyl radical generation via photoreduction of a simple pyridine N-oxide by an NADH analogue

Supplementary files

Article information

Article type
Communication
Submitted
05 Jul 2005
Accepted
22 Jul 2005
First published
02 Aug 2005

Org. Biomol. Chem., 2005,3, 3263-3265

Hydroxyl radical generation via photoreduction of a simple pyridine N-oxide by an NADH analogue

I. Nakanishi, C. Nishizawa, K. Ohkubo, K. Takeshita, K. T. Suzuki, T. Ozawa, S. M. Hecht, M. Tanno, S. Sueyoshi, N. Miyata, H. Okuda, S. Fukuzumi, N. Ikota and K. Fukuhara, Org. Biomol. Chem., 2005, 3, 3263 DOI: 10.1039/B509447J

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