Issue 16, 2014

A direct access to bioactive fused N-heterocyclic acetic acid derivatives

Abstract

A Cu-catalyzed new sequence involving the Ullmann type intermolecular C–C followed by an intramolecular C–N coupling and then intramolecular aza-Michael type addition (and oxidation) in a single pot afforded various fused N-heterocyclic acetic acid derivatives as inhibitors of PDE4.

Graphical abstract: A direct access to bioactive fused N-heterocyclic acetic acid derivatives

Supplementary files

Article information

Article type
Communication
Submitted
19 Dec 2013
Accepted
23 Jan 2014
First published
23 Jan 2014

Org. Biomol. Chem., 2014,12, 2514-2518

A direct access to bioactive fused N-heterocyclic acetic acid derivatives

R. Adepu, A. Rajitha, D. Ahuja, A. K. Sharma, B. Ramudu, R. Kapavarapu, K. V. L. Parsa and M. Pal, Org. Biomol. Chem., 2014, 12, 2514 DOI: 10.1039/C3OB42535E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements