Facile oxidative cyclization to access C2-quaternary 2-hydroxy-indolin-3-ones: synthetic studies towards matemone?
New Journal of Chemistry Pub Date: 2017-09-01 DOI: 10.1039/C7NJ02246H
Abstract
A concise and facile approach for the construction of 2-hydroxy-2-substituted indol-3-ones was developed through an oxidative cyclization of 2-aminophenyl-1,3-dione. Using CAN and TEMPO as oxidants, C2-quaternary 2-hydroxy-indolin-3-ones were efficiently installed in moderate to excellent yields (up to 99%). Moreover, this developed protocol was further applied to synthetic studies towards natural product matemone by starting from readily available 2-amino-4-bromobenzoic acid, and the precursor for matemone was efficiently installed.
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Journal Name:New Journal of Chemistry
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CAS no.: 89640-58-4