A new way for synthesis of phenoxazine and diphenoxazine derivatives via electrochemical method

1Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

Electrochemical oxidation of hydroquinone (1a) and 2,3-dimethylhydroquinone (1b) have been studied in the presence of 2-aminophenol (3a) and 2-amino-4-chlorophenol (3b), as nucleophiles in phosphate buffer solution (pH 7.2) using cyclic voltammetry and controlled potential coulometry. We proposed different mechanisms for the electrode process. The products were derived with good yield and purity using controlled-potential electrochemical oxidation of 1a, b in the presence of 3a and 3b at the graphite electrode in an undivided cell. © 2011 Pharmaceutical Society of Japan.

Cite

CITATION STYLE

APA

Hosseiny Davarani, S. S., Kalate Bojdi, M., & Mehdinia, A. (2011). A new way for synthesis of phenoxazine and diphenoxazine derivatives via electrochemical method. Chemical and Pharmaceutical Bulletin, 59(10), 1209–1213. https://doi.org/10.1248/cpb.59.1209

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free