Synthesis and antiplasmodial activity in vitro of new ferrocene-chloro-quine analogues
Beagley, P.; Blackie, M. A. L.; Chibale, K.; Clarkson, C.; Meijboom, R.; Moss, J. R.; Smith, P.; Su, H. Synthesis and antiplasmodial activity in vitro of new ferrocene-chloro-quine analogues. J. Chem. Soc., Dalton Trans. 2003, 3046-3051.
Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities
Ma, Z.; Hano, Y.; Nomura, T.; Chen, Y. Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities. Bioorg. Med. Chem. Lett. 2004, 14, 1193-1196.
5-Substituted, 6-substituted, and unsubstituted 3-heteroaromatic pyridine analogues of nicotine as selective inhibitors of cytochrome P-450 2A6
Denton, T. T.; Zhang, X.; Cashman, J. R. 5-Substituted, 6-substituted, and unsubstituted 3-heteroaromatic pyridine analogues of nicotine as selective inhibitors of cytochrome P-450 2A6. J. Med. Chem. 2005, 48, 224-239.
Megistoquinones i and II: Two quinoline alkaloids with antibacterial activity from the bark of Sarcomelicope megistophylla
Fokialakis, N.; Magiatis, P.; Chinou, L.; Mitaku, S.; Tillequin, F. Megistoquinones I and II: Two quinoline alkaloids with antibacterial activity from the bark of Sarcomelicope megistophylla. Chem. Pharm. Bull. 2002, 50, 413-414.
Synthesis and in vitro and in vivo antimalarial activity of N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine derivatives
Ryckebusch, A.; Derprez-Poulain, R.; Maes, L.; Debreu-Fontaine, M. A.; Mouray, E.; Grellier, P.; Sergheraert, C. Synthesis and in vitro and in vivo antimalarial activity of N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl) piperazine derivatives. J. Med. Chem. 2003, 46, 542-557.
Anticancer activity for 4,4-dihydroxybenzophenone-2,4- dinitrophenylhydrazone (A-007) analogues and their abilities to interact with lymphoendothelial cell surface markers
Morgan, L. R.; Jursic, B. S.; Hooper, C. L.; Neumann, D. M.; Thangaraj, K.; Leblanc, B. Anticancer activity for 4,4-dihydroxybenzophenone-2,4- dinitrophenylhydrazone (A-007) analogues and their abilities to interact with lymphoendothelial cell surface markers. Bioorg. Med. Chem. Lett. 2002, 12, 3407-3411.
New conjugated polymers with donor-acceptor architectures: Synthesis and photophysics of carbazole-quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer
Jenekhe, S. A.; Lu, L.; Alam, M. M. New conjugated polymers with donor-acceptor architectures: Synthesis and photophysics of carbazole-quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer. Macromole-cules 2001, 34, 7315-7324.
An efficient one-potti three-component synthesis of indeno[1,2-b] quinoline-9,11(6H,10H)-dione, acridine-1,8(2H,5H)-dione, and quinoline-3-carbonitrile derivatives from enaminones
Tu, S.-J.; Jiang, B.; Jia, R.-H.; Zhang, Y.; Yao, C.-S.; Shi, F. An efficient one-pot, three-component synthesis of indeno[1,2-b]quinoline-9,11(6H, 10H)-dione, acridine-1,8(2H,5H)-dione, and quinoline-3-carbonitrile derivatives from enaminones. Org. Biomol. Chem. 2006, 4, 3664-3668.
Facile heteropolyacid-promoted synthesis of 14-substituted-14-H- dibenzo[a,j] xanthene derivatives under solvent-free conditions
Heravi, M. M.; Bakhtiari, K.; Daroogheha, Z.; Bamoharram, F. F. Facile heteropolyacid-promoted synthesis of 14-substituted-14-H-dibenzo[a,j] xanthene derivatives under solvent-free conditions. J. Mol. Catal. A: Chem. 2007, 273, 99-101.
An efficient and chemoselective synthesis of acylals from aromatic aldehydes and their regeneration, catalyzed by 12-molyb-dophosphoric acid
Heravi, M. M.; Bakhtiari, K.; Bamoharram, F. F. An efficient and chemoselective synthesis of acylals from aromatic aldehydes and their regeneration, catalyzed by 12-molyb-dophosphoric acid. Catal. Commun. 2006, 7, 499-501.
12-Molybdophosphoric acid: A recyclable catalyst for the synthesis of Biginelli-type 3,4-dihydropyrimidine-2(1H)-ones
Heravi, M. M.; Bakhtiari, K.; Bamoharram, F. F. 12-Molybdophosphoric acid: A recyclable catalyst for the synthesis of Biginelli-type 3,4-dihydropyrimidine-2(1H)-ones. Catal. Commun. 2006, 7, 373-376.
A catalytic method for synthesis of Biginelli-type 3,4-dihydropyrimidin-2 (1H)-one using 12-tungstophosphoric acid
Heravi, M. M.; Derikvand, F.; Bamoharram, F. F. A catalytic method for synthesis of Biginelli-type 3,4-dihydropyrimidin-2 (1H)-one using 12-tungstophosphoric acid. J. Mol. Catal. A: Chem. 2005, 242, 173-175.