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

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.

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Veröffentlicht in:RSC advances 2015-01, Vol.5 (46), p.36902-36905
Hauptverfasser: Murugan, Kannan, Chinnapattu, Murugan, Nawaz Khan, Fazlur-Rahman, Iyer, Pravin S.
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Sprache:eng
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Zusammenfassung: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.
ISSN:2046-2069
2046-2069
DOI:10.1039/C5RA05755H