An efficient synthesis of 2,3-diaryl (3H)-quinazolin-4-ones via imidoyl chlorides
暂无分享,去创建一个
[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 .