An efficient synthesis of 2,3-diaryl (3H)-quinazolin-4-ones via imidoyl chlorides

[1]  P. Reddy,et al.  Synthesis of Some Novel 1,3,4‐Oxadiazol‐2‐yl‐4(3H)‐quinazolinones , 2007 .

[2]  Astrid A. Ortiz,et al.  Quinazolinone derivatives as orally available ghrelin receptor antagonists for the treatment of diabetes and obesity. , 2007, Journal of medicinal chemistry.

[3]  E. Seguin,et al.  Rapid synthesis of 2,3-disubstituted-quinazolin-4-ones enhanced by microwave-assisted decomposition of formamide , 2007 .

[4]  A. Judkins,et al.  A novel highly stereoselective synthesis of 2,3-disubstituted 3H-quinazoline-4-one derivatives. , 2007, Organic letters.

[5]  M. Zolfigol,et al.  A new approach to the facile synthesis of mono- and disubstituted quinazolin-4(3H)-ones under solvent-free conditions , 2005 .

[6]  W. Heaton,et al.  3H-Quinazolin-4-ones as a new calcilytic template for the potential treatment of osteoporosis. , 2005, Bioorganic & medicinal chemistry letters.

[7]  Libing Yu,et al.  Microwave-assisted one-pot synthesis of 2,3-disubstituted 3 H-quinazolin-4-ones , 2005 .

[8]  S. Xue,et al.  A facile synthesis of C2,N3-disubstituted-4-quinazolone. , 2004, The Journal of organic chemistry.

[9]  T. Hancox,et al.  Studies on quinazolinones as dual inhibitors of Pgp and MRP1 in multidrug resistance. , 2002, Bioorganic & medicinal chemistry letters.

[10]  Y. Wataya,et al.  Synthesis and antimalarial activity of febrifugine derivatives. , 2001, Chemical & pharmaceutical bulletin.

[11]  Hye-Sook Kim,et al.  Asymmetric synthesis of (+)-febrifugine and (+)-isofebrifugine using yeast reduction , 2001 .

[12]  Alper,et al.  Palladium-catalyzed cyclocarbonylation of o-iodoanilines with heterocumulenes: regioselective preparation of 4(3H)-quinazolinone derivatives , 2000, The Journal of organic chemistry.

[13]  Y. Wataya,et al.  New type of febrifugine analogues, bearing a quinolizidine moiety, show potent antimalarial activity against Plasmodium malaria parasite. , 1999, Journal of medicinal chemistry.

[14]  D. Dexter,et al.  Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization. , 1990, Journal of medicinal chemistry.

[15]  G. Coppola The Chemistry of Isatoic Anhydride , 1980 .

[16]  L. Errede Acylanthranils. I. The pathway of quinazolone formation in the reaction of acylanthranils with anilines , 1976 .