Issue 77, 2016

Convenient one-step synthesis of pyrrolo[3,4-c]quinolin-1-ones via TMSCl-catalyzed cascade reactions of isatins and β-enamino ketones

Abstract

An efficient and facile synthesis of pyrrolo[3,4-c]quinoline-1-ones by TMSCl-catalyzed reaction of easily available substituted isatins and β-enamino ketone derivatives has been developed. This cascade reaction has shown good functional group tolerance, operational simplicity, and proceeded smoothly in good to excellent yields via a one-step method under mild conditions. Preliminary experiments on oxidative cleavage of the C[double bond, length as m-dash]C bond have been applied.

Graphical abstract: Convenient one-step synthesis of pyrrolo[3,4-c]quinolin-1-ones via TMSCl-catalyzed cascade reactions of isatins and β-enamino ketones

Supplementary files

Article information

Article type
Communication
Submitted
14 Jun 2016
Accepted
27 Jul 2016
First published
28 Jul 2016

RSC Adv., 2016,6, 73760-73768

Convenient one-step synthesis of pyrrolo[3,4-c]quinolin-1-ones via TMSCl-catalyzed cascade reactions of isatins and β-enamino ketones

H. Xu, P. Zhou, B. Zhou, J. Zhou, Y. Shen, L. Lu and F. Yu, RSC Adv., 2016, 6, 73760 DOI: 10.1039/C6RA15492A

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