Диссертация (1155371), страница 20
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СПИСОК ЛИТЕРАТУРЫ1Kemnitzer W., Drewe J., Jiang S., Zhang H., Wang Y., Zhao J., Jia S., Herich J., Labreque D., StorerR., Meerovitch K., Bouffard D., Rej R., Denis R., Blais Ch., Lamothe S., Attardo G., Gourdeau H.,Tseng B., Kasibhatla Sh., and Sui Xiong Cai. Discovery of 4-aryl-4H-chromenes as a new series ofapoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activityrelationships of the 4-aryl group.
// J. Med. Chem. – 2004. – Vol. 47. – P. 6299-6310.2Anderson D.R., Hegde Sh., Reinhard E., Gomez L., Vernier W.F., Lee L., Liu Sh., Sambandam A.,Snidera P.A., Masih L. Aminocyanopyridine inhibitors of mitogen activated protein kinase-activatedprotein kinase 2 (MK-2). // Bioorg. Med. Chem. Lett. – 2005. – Vol. 15. – P.
1587-1590.3Reddy T.R., Reddy L.S, Reddy G.R., Nuthalapati V.N., Lingappa Y., Sandra S., Kapavarapu R., MisraP., Pal M. A Pd-mediated new strategy to functionalized 2-aminochromenes: their in vitro evaluation aspotential anti tuberculosis agents. // Bioorg. Med. Chem. Lett. – 2011. – Vol. 21. – P. 6433-6439.4Ashraf H. F. Abd El-Wahab. Synthesis, reactions and evaluation of the antimicrobial activity of some4-(p-halophenyl)-4H-naphthopyran, pyranopyrimidine and pyranotriazolopyrimidine derivatives. //Pharmaceuticals. – 2012.
– Vol. 5. – P. 745-757.5Khafagy M.M., Ashraf H.F. Abd El-Wahab, Eid F.A., El-Agrody A.M. Synthesis of halogenderivatives of benzo[h]chromene and benzo[a]anthracene with promising antimicrobial activities. // IlFarmaco. – 2002. – Vol. 57. – P. 715-722.Raić-Malić S., Tomašković L., Mrvoš-Sermek D., Prugovečki B., Cetina M., Grdiša M., Kresˇimir6Pavelić K., Mannschreck A., Balzarini J., De Clercq E., Mintas M. Spirobipyridopyrans,spirobinaphthopyrans,indolinospiropyridopyrans,indolinospironaphthopyransandindolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviralevaluation. // Bioorg.
Med. Chem. – 2004. – Vol. 12. – P. 1037-1045.7Brastianos H.C., Vottero E., Patrick B.O., Van Soest R., Matainaho T., Mauk A.G., Andersen R.J.Exiguamine A, an indoleamine-2,3-dioxygenase (IDO) inhibitor isolated from the marine spongeNeopetrosia exigua. // J. Am. Chem. Soc. – 2006.
– Vol. 128. – P. 16046-16047.8Kolla S. R., Lee Y.R. Ca(OH)2-mediated efficient synthesis of 2-amino-5-hydroxy-4H-chromenederivatives with various substituents. // Tetrahedron. – 2011. – Vol. 67. – P. 8271-8275.9Mortikov V. Yu., Rodinovskaya L. A., Fedorov A. E., Shestopalov A. M., Belyakov P. A. Synthesisof heterocyclic compounds from 4-formylpyrazoles. // Russ. Chem. Bull. – 2014. – Vol. 63. – No. 2 –P. 443—456.10Mkaouar K., Chabchoub F., Samadi A., Contelles J.
L. M., Salem M. Convenient synthesis of 11-aryl-1,12-dihydro-11H-naphthopyrano[2,3-d]pyrimidin-12-ones. // Synth. Commun. – 2010. – Vol. 40.– P. 3405–3414.11111El-Agrody A. M., Abd-Rabboh H. S.M., Al-Ghamdi A.M. Synthesis, antitumor activity, andstructure–activity relationship of some 4H-pyrano[3,2-h]quinoline and 7H-pyrimido[4’,5’:6,5]pyrano[3,2-h]quinoline derivatives. // Med. Chem. Res. – 2013. – Vol.
22. – P. 1339–1355.12Gholipour S., Davoodnia A., Nakhaei-Moghaddam M. Synthesis, characterization, and antibacterialevaluation of new alkyl 2-amino-4-aryl-4H-chromene-3-carboxylates. // Chem. Heterocycl. Compd. –2015. – Vol. 51. – No. 9. – P. 808–813.13Meng X.-Y., Wang H.-J., Wang Ch.-P., Zhang Zh.-H. Disodium hydrogen phosphate as an efficientand cheap catalyst for the synthesis of 2-aminochromenes. // Synth. Commun. – 2011. – Vol. 41. – P.3477–3484.14Ameen M.A., Motamed S.M., Abdel-latif F.F.
Highly efficient one-pot synthesis of dihydropyranheterocycles. // Chin.Chem. Lett. – 2014. – Vol. 25. – P. 212–214.15Kumar A., Sharma S., Maurya R.A., Sarkar J. Diversity oriented synthesis of benzoxanthene andbenzochromene libraries via one-pot, three-component reactions and their anti-proliferative activity. //J. Comb. Chem. – 2010. – Vol. 12. – P. 20–24.16Maleki B., Sheikh S. One-pot synthesis of 2-amino-2-chromene and 2-Amino-3-cyano-4H-pyranderivatives promoted by potassium fluoride. // Org. Prep.
Proced. Int. – 2015. – Vol. 47. – P. 368–378.17Mosaddegh E. Ultrasonic-assisted preparation of nano eggshell powder: A novel catalystin green and high efficient synthesis of 2-aminochromenes. // Ultrason. Sonochem. – 2013. – Vol. 20. –P. 1436–1441.18Hossaini Z., Sheikholeslami-Farahani F., Soltani S., Sayyed-Alangi S.Z., Sajjadi-Ghotabadi H. ZnOnanoparticles as a highly efficient heterogeneous catalyst for the synthesis of various chromene andpyrano[4,3-b]pyran derivatives under solvent-free conditions. // Chem. Heterocycl. Compd.
– 2015. –Vol. 51. – No. 1. – P. 26–30.19Safari J., Zarnegar Z., Heydarian M. Magnetic Fe3O4 nanoparticles as efficient and reusable catalystfor the green synthesis of 2-amino-4H-chromene in aqueous media. // Bull. Chem. Soc. Jpn. – 2012. –Vol. 85. – No. 12.
– P. 1332-1338.20Eshghi H., Damavandi S., Zohuri G. H. Efficient one-pot synthesis of 2-amino-4H-chromenescatalyzed by ferric hydrogen sulfate and Zr-based catalysts of FI. // Synth. React. Inorg. Met.-Org. NanoMet. Chem. – 2011. – Vol. 41. – P. 1067–1073.21Behbahani F.K., Maryam S. On water CuSO4*5H2O-catalyzed synthesis of 2-amino-4H-chromenes.// J.
Korean Chem. Soc. – 2013. – Vol. 57. – No. 3. – P. 357-360.22Mehrabi H., Kamali N. Efficient and eco-friendly synthesis of 2-amino-4H-chromene derivativesusing catalytic amount of tetrabutylammonium chloride (TBAC) in water and solvent-free conditions. //J. Iran. Chem.
Soc. – 2012. – Vol. 9. – P. 599–605.11223Sabitha G., Bhikshapathi M., Nayak S., Srinivas R., Yadav J. S. Triton B catalyzed three-component,one-pot synthesis of 2-amino-2-chromenes at ambient temperature. // J. Heterocyclic. Chem. – 2011. –Vol. 48. – P. 267.24Patil S.A., Wang J., Li X.S., Chen J., Jones T.S., Hosni-Ahmed A., Patil R., Seibel W.L., Li W., MillerD.D. New substituted 4H-chromenes as anticancer agents. // Bioorg. Med.
Chem. Lett. – 2012. – Vol.22. – P. 4458–4461.25Khan Md. N., Pal S., Karamthulla Sh., Choudhury L.H. Imidazole as organocatalyst formulticomponent reactions: diversity oriented synthesis of functionalized hetero- and carbocycles usingin situ-generated benzylidenemalononitrile derivatives. // RSC Adv. – 2014. – Vol. 4. – P. 3732-3741.26Khurana J.M., Nand Bh., Saluja P. DBU: a highly efficient catalyst for one-pot synthesis of substituted3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenesand 2-amino-4H-benzo[g]chromenes in aqueous medium. // Tetrahedron. – 2010. – Vol. 66.
– P. 56375641.27Behbahani F.K., Mehraban S. Synthesis of 2-amino-3-cyano-7-hydroxy-4H-chromenes using L-Proline as a biocatalyst. // J. Korean Chem. Soc. – 2015. – Vol. 59. – No. 4. – P. 284-288.28Verma S., Jain S.L. Thiourea dioxide catalyzed multi-component coupling reaction for the one stepsynthesis of naphthopyran derivatives. // Tetrahedron Lett. – 2012.
– Vol. 53. – P. 6055–6058.29Dekamin M.G., Eslami M., Maleki A. Potassium phthalimide-N-oxyl: a novel, efficient, and simpleorganocatalyst for the one-pot three-component synthesis of various 2-amino-4H-chromene derivativesin water. // Tetrahedron. – 2013. – Vol. 69. – P. 1074-1085.30Ghorbani M., Noura S., Oftadeha M., Zolfigol M.A., Soleimani M.H. Preparation of neutral ionicliquid [2-Eim]OAc with dual catalytic-solvent system roles for the synthesis of 2-amino-3-cyano-7hydroxy-4-(aryl)-4H-chromene derivatives. // J. Mol.
Liq. – 2015. – Vol. 212. – P. 291–300.31Shaterian H.R., Aghakhanizadeh M. Ionic-liquid-catalyzed green synthesis of coumarin derivativesunder solvent-free conditions. // Chin. J. Catal. – 2013. – Vol. 34. – P. 1690-1696.32Mahmoodi M., Aliabadi A., Emami S., Safavi M., Rajabalian S., Mohagheghi M.-A., Khoshzaban A.,Samzadeh-Kermani A., Lamei N., Shafiee A., Foroumadi A. Synthesis and in-vitro cytotoxicity of polyfunctionalized 4-(2-arylthiazol-4-yl)-4H-chromenes. // Arch.
Pharm. Chem. Life Sci. – 2010. – Vol. 343.– P. 411 – 416.32Akbarzadeh T., Rafinejad A., MollaghasemJ.M., Safavi M., Fallah-Tafti A., Pordeli M., ArdestaniS.K., Shafiee A., Foroumadi A. 2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes: synthesis andin vitro cytotoxic activity. // Arch. Pharm.