Issue 89, 2012
From the journal:

Chemical Communications

Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement†

Chandan Dey,a   Dmitry Katayev,a   Kai E. O. Ylijokia  and  E. Peter Kündig*a  

* Corresponding authors

a Department of Organic Chemistry, University of Geneva, 30 Quai Ernest Ansermet, 1211 Geneva 4, Switzerland
E-mail: peter.kundig@unige.ch
Web: http://www.unige.ch/sciences/chiorg/kundig/
Fax: +41 22-379-3215
Tel: +41 22-379-6093

Abstract

A novel efficient NaOtBu-mediated protocol for the synthesis of 3,3-disubstituted aza-oxindoles proceeds via a Truce–Smiles rearrangement–cyclisation pathway.

Graphical abstract: Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement

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Article information

DOI
https://doi.org/10.1039/C2CC36068C
Article type
Communication
Submitted
21 Aug 2012
Accepted
12 Sep 2012
First published
13 Sep 2012

Chem. Commun., 2012,48, 10957-10959

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Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement

C. Dey, D. Katayev, K. E. O. Ylijoki and E. P. Kündig, Chem. Commun., 2012, 48, 10957 DOI: 10.1039/C2CC36068C

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