YAKUGAKU ZASSHI
Online ISSN : 1347-5231
Print ISSN : 0031-6903
ISSN-L : 0031-6903
Products in the Fluorometric Reaction of Purines with 4, 5-Dimethyl-o-phenylenediamine after Oxidation Using N-Bromosuccinimide
Masatoki KATAYAMAHirokazu TANIGUCHI
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1990 Volume 110 Issue 10 Pages 776-782

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Abstract

Twelve purines oxidized with 4, 5-dimethyl-o-phenylenediamine (DMPD) was found to react with N-bromosuccinimide (NBS) to give fluorescent derivatives. In this paper, the identification of oxidation and fluorescent products have been described. In compliance with the substituent on purine skelton, three alloxans were obtained from twelve purines after oxidation by using NBS. The three alloxans reacted with DMPD to form two quinoxalines and an alloxazine, all of which being fluorescent.

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© by the PHARMACEUTICAL SOCIETY OF JAPAN
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