Quinoline and quinazoline alkaloids, two important classes of N-based heterocyclic
compounds, have attracted scientific and popular interest worldwide since the 19th century …

Among the N‐containing heterocyclic compounds, quinazoline‐4‐(3H)‐one derivatives
have been the center of attraction of medicinal and synthetic chemists due to their excellent …

An efficient synthesis of enantioenriched hydroquinazoline cores via a novel bifunctional
iminophosphorane squaramide catalyzed intramolecular aza-Michael reaction of urea …

For the first time, quinazolin-4 (3 H)-one-based cationic surfactants were prepared and fully
characterized by IR and NMR spectroscopic techniques and elemental analysis. Some of …

A catalyst-free microwave-assisted annulation protocol for the preparation of biologically
interesting pyrido-fused quinazolinones and pyrido [1, 2-a] benzimidazoles is developed …

An efficient protocol for the introduction of acetoxy and hydroxy functionalities on unactivated
aryl sp2 carbons of oxobenzoxazine derivatives via an ortho-C–H activation reaction using a …

Two novel compounds [Ni (PQC) 2 (H 2 O) 2]. H 2 O and [Cu (PQC) 2] where PQC= 2–
phenylquinazoline–4–carboxylate have been synthesized. Magnetic susceptibility …

Lemon juice has been extensively explored recently as highly selective and efficient
biocatalyst as well as green solvent in organic synthesis. Lemon juice holds considerable …

Cross-dehydrogenative coupling reactions have been utilized to alkylate 4 (3H)-
quinazolinones with ethers and amides, using catalytic n-Bu4NI and t-BuOOH as oxidants …

An efficient protocol for obtaining fused quinazolinones through an oxidative free-radical
cyclization under metal-and tin-free conditions is described. The oxidative cyclization of …