Radical-promoted cyclization of 3-allyl-2-arylquinazolinones mediated by silver(i) salts to access SCF3/SCN-enriched dihydroisoquinolino[1,2-b]quinazolinones

Abstract

Herein, we describe an efficient approach for the synthesis of SCF3- and SCN-functionalized polycyclic dihydroisoquinolino[1,2-b]quinazolinones through radical-mediated thio-functionalization of allylic alkenes followed by intramolecular cyclization. The transformation proceeds through sulfur-radical-triggered C–S and C–C bond formation, providing an efficient route to sulfur- and fluorine-enriched polycyclic quinazolinones. Moreover, this strategy offers high atom economy, operational simplicity, and broad substrate compatibility.

Graphical abstract: Radical-promoted cyclization of 3-allyl-2-arylquinazolinones mediated by silver(i) salts to access SCF3/SCN-enriched dihydroisoquinolino[1,2-b]quinazolinones

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Article information

Article type
Communication
Submitted
07 Nov 2025
Accepted
16 Jan 2026
First published
21 Jan 2026

Org. Biomol. Chem., 2026, Advance Article

Radical-promoted cyclization of 3-allyl-2-arylquinazolinones mediated by silver(I) salts to access SCF3/SCN-enriched dihydroisoquinolino[1,2-b]quinazolinones

V. Vara, K. R. Thete, A. A. Khan and M. Muthukrishnan, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D5OB01755F

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