Microwave-induced CAN promoted atom-economic synthesis of 1H-benzo[b]xanthene and 4H-benzo[g]chromene derivatives of N-allyl quinolone and their antimicrobial activity
ANTIMICROBIAL ACTIVITY;
ARTICLE;
ATOM;
CALCULATION;
CATALYSIS;
CHEMICAL REACTION;
DRUG SYNTHESIS;
METHODOLOGY;
MICROWAVE RADIATION;
NONHUMAN;
ONE POT THREE COMPONENT REACTION;
STRUCTURE ACTIVITY RELATION;
Chen LG, Yang LL, Wang CC (2008) Anti-inflammatory activity of mangostins from Garcinia mangostana. Food Chem Toxicol 46:688-693. doi: 10.1016/j.fct.2007.09.096
Synthesis, structure-activity relationship of novel substituted 4H-chromen-1,2,3,4-tetrahydropyrimidine-5-carboxylates as potential antimycobacterial and anticancer agents
China Raju B, Nageswara Rao R, Suman P et al (2011) Synthesis, structure-activity relationship of novel substituted 4H-chromen-1,2,3,4- tetrahydropyrimidine-5-carboxylates as potential antimycobacterial and anticancer agents. Bioorg Med Chem Lett 21:2855-2859. doi: 10.1016/j.bmcl.2011. 03.079
Dabiri M, Tisseh ZN, Bazgir A (2010) An efficient three-component synthesis of benzoxanthenes in water. J Heterocycl Chem 47:1062-1065. doi: 10.1002/jhet.420
Edmont D, Rocher R, Plisson C, Chenault J (2000) Synthesis and evaluation of quinoline carboxyguanidines as antidiabetic agents. Bioorg Med Chem Lett 10:1831-1834. doi: 10.1016/S0960-894X(00)00354-1
A facile regioselective synthesis of novel spiro-thioxanthene and spiro-xanthene-9′,2-[1,3,4]thiadiazole derivatives as potential analgesic and anti-inflammatory agents
Hafez HN, Hegab MI, Ahmed-Farag IS, El-Gazzar ABA (2008) A facile regioselective synthesis of novel spiro-thioxanthene and spiro-xanthene- 9′,2-[1,3,4]thiadiazole derivatives as potential analgesic and anti-inflammatory agents. Bioorg Med Chem Lett 18:4538-4543. doi: 10.1016/j.bmcl.2008.07.042
10.1111/j.1574-6976.2010.00247.x 20738404 10.1111/j.1574-6976.2010.00247. x 1:CAS:528:DC%2BC3MXjtVaitbo%3D
Heeb S, Fletcher MP, Chhabra SR et al (2011) Quinolones: from antibiotics to auto inducers. FEMS Microbiol Rev 35:247-274. doi: 10.1111/j.1574-6976.2010. 00247.x
Microwave-assisted CAN-catalyzed solvent-free synthesis of N-allyl quinolone-based pyrano[4,3-b]chromene and benzopyrano[3,2-c]chromene derivatives and their antimicrobial activity
doi: 10.1007/s00044-012-0085-z
Jardosh HH, Patel MP (2012) Microwave-assisted CAN-catalyzed solvent-free synthesis of N-allyl quinolone-based pyrano[4,3-b]chromene and benzopyrano[3,2-c]chromene derivatives and their antimicrobial activity. Med Chem Res. doi: 10.1007/s00044-012-0085-z
Microwave-assisted synthesis of 3′-indolyl substituted 4H-chromenes catalyzed by DMAP and their antimicrobial activity
doi: 10.1007/s00044-011-9861-4
Kathrotiya HG, Patel MP (2011) Microwave-assisted synthesis of 3′-indolyl substituted 4H-chromenes catalyzed by DMAP and their antimicrobial activity. Med Chem Res. doi: 10.1007/s00044-011-9861-4
DBU: A highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H-benzo[g]chromenes in aqueous medium
Khurana JM, Nand B, Saluja P (2010) DBU: a highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H-benzo[g]chromenes in aqueous medium. Tetrahedron 66:5637-5641. doi: 10.1016/j.tet.2010.05.082
Lambert RW, Martin JA, Merrett JH, Parkes EBK, Thomas GJ (1997) Preparation of pyrimidine nucleosides as thymidine kinase inhibitors and virucides. PCT Int Appl WO9706178
Lucero B, Regina C, Frugulhetti I et al (2006) Synthesis and anti-HSV-1 activity of quinolonic acyclovir analogues. Bioorg Med Chem Lett 16:1010-1013. doi: 10.1016/j.bmcl.2005.10.111
Synthesis and identification of β-aryloxyquinolines and their pyrano[3,2-c]chromene derivatives as a new class of antimicrobial and antituberculosis agents
Mungra DC, Patel MP, Rajani DP, Patel RG (2011) Synthesis and identification of β-aryloxyquinolines and their pyrano[3,2-c]chromene derivatives as a new class of antimicrobial and antituberculosis agents. Eur J Med Chem 46:4192-4200. doi: 10.1016/j.ejmech.2011.06.022
O'Donnell F, Smyth TJP, Ramachandran VN, Smyth WF (2010) A study of the antimicrobial activity of selected synthetic and naturally occurring quinolines. Int J Antimicrob Agents 35:30-38. doi: 10.1016/j.ijantimicag.2009.06.031
Praveen C, Ayyanar A, Perumal PT (2011) Practical synthesis, anticonvulsant, and antimicrobial activity of N-allyl and N-propargyl di(indolyl)indolin-2-ones. Bioorg Med Chem Lett 21:4072-4077. doi: 10.1016/j.bmcl.2011.04.117
Ceric ammonium nitrate (CAN) promoted efficient solid phase synthesis of amide derivatives: A green approach
Reddy CS, Raghu M, Nagaraj A (2008) Ceric ammonium nitrate (CAN) promoted efficient solid phase synthesis of amide derivatives: a green approach. Indian J Chem B 47:315-318
Shaabani A, Ghadari R, Ghasemi S et al (2009) Novel one-pot three- and pseudo-five-component reactions: synthesis of functionalized benzo[g]- and dihydropyrano[2,3-g]chromene derivatives. J Comb Chem 11:956-959. doi: 10.1021/cc900101w
Shafiee A, Motamedi R, Firuzi O et al (2011) Synthesis and cytotoxic activity of novel benzopyrano[3,2-c]chromene-6,8-dione derivatives. Med Chem Res 20:466-474. doi: 10.1007/s00044-010-9340-3
DABCO-promoted three-component regioselective synthesis of functionalized chromen-5-ones and pyrano[3,2-c]chromen-5-ones via direct annulation of α-oxoketene-N,S-arylaminoacetals under solvent-free conditions
Singh MS, Nandi GC, Samai S (2012) DABCO-promoted three-component regioselective synthesis of functionalized chromen-5-ones and pyrano[3,2-c]chromen-5-ones via direct annulation of α-oxoketene-N,S- arylaminoacetals under solvent-free conditions. Green Chem 14:447-455. doi: 10.1039/c1gc16129f
Soleimani E, Khodaei MM, Koshvandi ATK (2011) The efficient synthesis of 14-alkyl or aryl 14H-dibenzo[a, j]xanthenes catalyzed by bismuth(III)chloride under solvent-free conditions. Chin Chem Lett 22:927-930. doi: 10.1016/j.cclet.2011.01.012
Tabarrini O, Massari S, Daelemans D et al (2008) Structure-activity relationship study on anti-HIV 6-desfluoroquinolones. J Med Chem 51:5454-5458. doi: 10.1021/jm701585h
Synthesis and antimicrobial activity of some new N-substituted quinoline derivatives of 1H-pyrazole
10.1002/ardp.201000010 10.1002/ardp.201000010
Thumar NJ, Patel MP (2011) Synthesis and antimicrobial activity of some new N-substituted quinoline derivatives of 1H-pyrazole. Arch Pharm Chem Life Sci 2:91-101. doi: 10.1002/ardp.201000010
Xia Y, Yang Z, Xia P et al (2003) Antitumor agents. Part 226: synthesis and cytotoxicity of 2-phenyl-4-quinolone acetic acids and their esters. Bioorg Med Chem Lett 13:2891-2893. doi: 10.1016/S0960-894X(03)00624-3
An efficient synthesis of 4H-benzo[g]chromene-5,10-dione derivatives through triethylbenzylammonium chloride catalyzed multicomponent reaction under solvent-free conditions
Yao C, Yu C, Li T, Tu S (2009) An efficient synthesis of 4H-benzo[g]chromene-5,10-dione derivatives through triethylbenzylammonium chloride catalyzed multicomponent reaction under solvent-free conditions. Chin J Chem 27:1989-1994. doi: 10.1002/cjoc.200990334