The 4 (3H)-quinazolinone is a frequently encountered heterocycle with broad applications
including antimalarial, antitumor, anticonvulsant, fungicidal, antimicrobial, and anti …

A facile, copper-mediated, direct C–H (sp2)/C–H (sp3) bond coupling of benzoic acid
derivatives with ethyl cyanoacetate by the deployment of an 8-aminoquinoline moiety as a …

Imidazolium chloride as an environmentally benign additive efficiently facilitates construction
of 4 (3H)-quinazolinones using anthranilamides and DMF derivatives. A series of 4 (3H) …

A novel, practical, highly efficient, and transition metal free nitrogen insertion reaction for the
synthesis of 2, 3-disubstituted quinazolinone derivatives was developed. Diverse …

A simple and efficient copper-catalyzed method for the synthesis of 11H-benzo [a]
carbazoles has been developed. The protocol uses readily available substituted 2-(2 …

A novel series of 6-iodo-2-methylquinazolin-4-(3H)-one derivatives, 3a–n, were synthesized
and evaluated for their in vitro cytotoxic activity. Compounds 3a, 3b, 3d, 3e, and 3h showed …

Facile assembly of two 6-membered fused N -heterocyclic rings: a rapid access to novel small
molecules via Cu-mediated reaction - Chemical Communications (RSC Publishing) …

An efficient approach for the synthesis of benzo-fused pyridoindolone derivatives via a one-
pot copper catalyzed tandem reaction of 2-iodobenzamides with 2-iodobenzylcyanides has …

Copper‐catalyzed base switching procedures for the synthesis of various fused
isoquinolinone derivatives and iminoisoindolinone derivatives from the same starting …

A CuI-catalyzed tandem reaction of 5-(2-bromoaryl)-N-aryl-1 H-pyrazol-3-amines with active
acetonitrile derivatives to prepare pyrazolo [5, 1-a] isoquinolines in good to excellent yields …