Quinazolinone, a bicyclic compound, comprises a pyrimidine ring fused at 4´ and 8´
positions with a benzene ring and constitutes a substantial class of nitrogen-containing …

A Cp* CoIII-catalyzed arene C–H bond amidation/annulation of benzamides was developed
to afford quinazolinone derivatives in one-pot with high yields and broad substrate scope …

A palladium-catalyzed four-component carbonylative cyclization reaction for the synthesis of
2, 3-disubstituted quinazolin-4 (3H)-ones has been developed. A range of different 2, 3 …

In the field of transition-metal-catalyzed C–H activation, N-methoxyamides are widely used
as C–H activation substrate. Unexpectedly, in this work N-methoxyamides were found to …

Free radical reactions represent an efficient and significant tool to construct organic
molecules by taking advantages of the high-efficiency, remarkable selectivity and good …

Herein, an eco‐friendly and atom‐economical electrochemical methodology with isatins and
1, 2, 3, 4‐tetrahydroisoquinolines through NHPI/O2‐mediated intermolecular …

A metal-free and efficient procedure for the synthesis of pyrrolo [1, 2-a] quinoxalines,
quinazolinones, and indolo [1, 2-a] quinoxaline has been developed. The key features of our …

A radical domino cyclisation reaction of N‐cyanamide alkenes, mediated by hydrogen atom
transfer (HAT) has been developed. This method, using PhSiH3 and catalytic Fe (acac) 3 …

A rhodium‐catalyzed synthesis of isoquinolino [1, 2‐b] quinazolines via C− H annulation
using vinylene carbonate as an oxidizing acetylene surrogate in biomass‐derived γ …

Quinoline derivatives are an important class of heterocyclic compounds and possess
various applications in synthetic organic chemistry, medicinal chemistry, material chemistry …