Moscow University Chemistry Bulletin Vol. 47, No. 6, P. 398 (2006)

S. A. Yamashkin, N. V. Zhukova, M. A. Yurovskaya

On the Reaction of Substituted 7-Aminoindoles with Oxalacetic Ester

Abstract

The interaction of unsubstituted at pyrrole nitrogen atom 2,3-dimethyl- and 2,3-dimethyl-6-methoxy-7-aminoindoles with oxalacetic ester lead to the new heterocyclic system pyrroloquinoxaline, whereas N-metylated analogue - 1,2,3-trimethyl-7-aminoindoles under same conditions yield corresponding enamine, which underwent of thermic cycization into pyrroloquinoline.

Moscow University Chemistry Bulletin.
2006, Vol. 47, No. 6, P. 398

Overview

Editorial board

Tables of Contents

Subscription

The site is supported by Russian Foundation for Basic Research
The using of published on this page materials is not allowed without special permission
Copyright (C) Chemisty Department of Moscow State University
Web-Editor: B.I.Pokrovskii
Web-design: Copyright (C) MIG and VVM
webmaster@www.chem.msu.su