Issue 46, 2015

Synthesis of novel benzoxaborinin-4-ones and its application in indolin-2-ones synthesis using a Suzuki–Miyaura reaction protocol

Abstract

We herein discuss the synthesis of novel benzoxaborinin-4-one from substituted isatins and 2-acetyl phenylboronic acid. Furthermore, we have demonstrated the application of these boronic acids to synthesize indolin-2-ones (Z isomer) regioselectively using Suzuki–Miyaura reaction.

Graphical abstract: Synthesis of novel benzoxaborinin-4-ones and its application in indolin-2-ones synthesis using a Suzuki–Miyaura reaction protocol

Supplementary files

Article information

Article type
Communication
Submitted
01 Apr 2015
Accepted
15 Apr 2015
First published
15 Apr 2015

RSC Adv., 2015,5, 36902-36905

Author version available

Synthesis of novel benzoxaborinin-4-ones and its application in indolin-2-ones synthesis using a Suzuki–Miyaura reaction protocol

K. Murugan, M. Chinnapattu, F. Nawaz Khan and P. S. Iyer, RSC Adv., 2015, 5, 36902 DOI: 10.1039/C5RA05755H

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