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Access to N-Fused Quinazolinones by Radical-Promoted Cascade Annulations of Alkenyl -Cyanamides with Aromatic Aldehydes. | LitMetric

Access to N-Fused Quinazolinones by Radical-Promoted Cascade Annulations of Alkenyl -Cyanamides with Aromatic Aldehydes.

J Org Chem

Institut de Chimie des Substances Naturelles (ICSN), CNRS UPR 2301, Université Paris-Saclay, 1 avenue de la Terrasse, 91198 Gif-sur-Yvette Cedex, France.

Published: May 2024

A cascade radical cyclization of alkenyl -cyanamides with aromatic aldehydes has been achieved for an expeditious synthesis of keto-methylated dihydropyrrolo-quinazolinones. Benzoyl radicals, generated from aryl aldehydes in the presence of di--butyl peroxide (DTBP), promoted the domino annulations leading to distinctive functionalized quinazolinones in good yields. In addition, the robustness of the present protocol is validated by employing heterocyclic and natural product-based aldehydes.

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Source
http://dx.doi.org/10.1021/acs.joc.4c00494DOI Listing

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