Issue 4, 2016

An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones

Abstract

An unprecedented reaction between indolin-2-ones and α-substituted ketones has been developed. Using this protocol, a wide range of biologically important 3-hydroxy-3-phenacyloxindole derivatives could be obtained in good yield (up to 93%) under mild reaction conditions. A possible mechanism of this reaction was tentatively proposed based on some control experiments and MS spectrometry analysis.

Graphical abstract: An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones

Supplementary files

Article information

Article type
Paper
Submitted
20 Nov 2015
Accepted
08 Dec 2015
First published
08 Dec 2015

Org. Biomol. Chem., 2016,14, 1395-1401

Author version available

An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones

M. Bai, Y. You, Y. Chen, G. Xiang, X. Xu, X. Zhang and W. Yuan, Org. Biomol. Chem., 2016, 14, 1395 DOI: 10.1039/C5OB02391B

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