TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion - Archive ouverte HAL Access content directly
Journal Articles Molecules Year : 2015

TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion

Abstract

We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones 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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hal-01234886 , version 1 (01-12-2015)

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Aïda R. Nadji-Boukrouche, Omar Khoumeri, Thierry Terme, Messaoud Liacha, Patrice Vanelle. TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion. Molecules, 2015, 20, pp.1262-1276. ⟨10.3390/molecules20011262⟩. ⟨hal-01234886⟩
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