Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor - Archive ouverte HAL
Article Dans Une Revue Beilstein Journal of Organic Chemistry Année : 2020

Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor

Résumé

A convergent strategy is reported for the construction of nitrogen-containing heterocycles from common substrates: 1,4-diketones and primary amines. Indeed, by just varying substrates, substituents or heating mode it is possible to selectively synthesize indole, indolone (1,5,6,7-tetradihydroindol-4-one) or cinnoline (5,6,7,8-tetrahydrocinnoline) derivatives in moderate to excellent yields.

Domaines

Chimie
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Dates et versions

hal-02901438 , version 1 (20-11-2020)

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Dalel El-Marrouki, Sabrina Touchet, Abderrahmen Abdelli, Hédi M’rabet, Mohamed Lotfi Efrit, et al.. Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor. Beilstein Journal of Organic Chemistry, 2020, 16, pp.1722-1731. ⟨10.3762/bjoc.16.144⟩. ⟨hal-02901438⟩
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