TDAE strategy in the benzoxazolone series: Synthesis and reactivity of a new benzoxazolinonic anion

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Abstract

We describe an original pathway to produce new 5-substituted 3-methyl-6-nitrobenzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy.

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Nadji-Boukrouche, A. R., Khoumeri, O., Terme, T., Liacha, M., & Vanelle, P. (2015). TDAE strategy in the benzoxazolone series: Synthesis and reactivity of a new benzoxazolinonic anion. Molecules, 20(1), 1262–1276. https://doi.org/10.3390/molecules20011262

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