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electroresection of some 1,4-diazaspiro [5.5] under ane-3-imino-5-ones in aqueous buffered media at Hg cathode
Bulletin of Faculty of Pharmacy-Cairo University. 1993; 31 (2): 153-57
in English | IMEMR | ID: emr-27543
ABSTRACT
The palarographic behavior of the title compounds in aqueous buffered media at DME was investigated. The mechanism of the electrode process was proposed and discussed. The identified resulting electrolysis product in high yield [70%] was the corresponding amino formed through the uptake of two electrons of the protonated imino, in a diffusion controlled irreversible process
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Index: IMEMR (Eastern Mediterranean) Main subject: Anticonvulsants Language: English Journal: Bull. Fac. Pharm.-Cairo Univ. Year: 1993

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Index: IMEMR (Eastern Mediterranean) Main subject: Anticonvulsants Language: English Journal: Bull. Fac. Pharm.-Cairo Univ. Year: 1993