Two-Step Synthetic Route to 10-Substituted Isoalloxazines

Autor: Roopali Rai, Prosenjit Chattopadhyay, Pramod S. Pandey
Rok vydání: 2006
Předmět:
Zdroj: ChemInform. 37
ISSN: 1522-2667
0931-7597
DOI: 10.1002/chin.200646203
Popis: 10‐Substituted isoalloxazines were synthesized in two steps starting from 1,2‐phenylenediamine. Monoalkylation of the diamine resulted in 2‐amino‐N‐alkylanilines, which were subsequently condensed with alloxan in boric acid and acetic acid to give 10‐substituted isoalloxazines.
Databáze: OpenAIRE