Диссертация (1155371), страница 22
Текст из файла (страница 22)
– Vol. 68. – P. 226-237.11669Kalla R.M.N., Byeon S.J., Heo M.S., Kim I. Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and 2-amino-4H-chromenes catalyzed by tetramethylguanidine. // Tetrahedron. – 2013.– Vol. 69. – P. 10544-10551.70Kulkarni M.A., Pandurangi V.R., Desai U.V., Wadgaonkar P.P. A practical and highly efficientprotocol for multicomponent synthesis of β-phosphonomalononitriles and 2-amino-4H-chromen-4-ylphosphonates using diethylamine as a novel organocatalyst.
// C. R. Chimie. – 2012. – Vol. 15. – P. 745–752.71Rajasekhar M., Rao K.U.M., Sundar Ch. S., Reddy N.B., Nayak S.K., Reddy C.S. Green synthesisand bioactivity of 2-amino-4H-chromen-4-ylphosphonates. // Chem. Pharm. Bull. – 2012. – Vol. 60. –Issue 7. – P. 854–858.72Das B., Balasubramanyam P., Reddy G. Ch., Salvanna N. Simple, efficient, and catalyst-free synthesisof (2-amino-4H-1-benzopyran-4-yl)phosphonates in polyethylene glycol. // HeIv. Chim. Acta.
– 2011.– Vol. 94. – P. 1347-1350.73Narayana Murthy S., Madhav B., Prakash Reddy V., Nageswar Y. V. D. One-pot synthesis of 2-amino-4H-chromen-4-yl phosphonate derivatives using β-cyclodextrin as reusable catalyst in water. //Tetrahedron Lett. – 2010. – Vol. 51. – P.
3649–3653.74Kalla R.M.N., Choi J.-S., Yoo J.-W., Byeon S.J., Heo M.S., Kim I. Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and their anticancer properties. // Eur. J. Med. Chem. – 2014. – Vol. 76.– P. 61-66.75Heravi M.M., Zakeri M., Moharami A. Versatile three-component procedure for combinatorialsynthesis of spiro-oxindoles with fused chromenes catalysed by L-proline. // J.
Chem. Sci. – 2012. –Vol. 124. – No. 4. – P. 865–869.76Azizi N., Dezfooli S., Hashemi M.M. Greener synthesis of spirooxindole in deep eutectic solvent. //J. Mol. Liq. – 2014. – Vol. 194. – P. 62–67.77Park J.H., Lee Y.R., Kim S.H. A novel synthesis of diverse 2-amino-5-hydroxy-4H-chromenederivatives with a spirooxindole nucleus by Ca(OH)2-mediated three-component reactions of substitutedresorcinols with isatins and malononitrile.
// Tetrahedron. – 2013. – Vol. 69. – P. 9682-9689.78Mahdavinia Gh. H., Mirzazadeh M., Notash B. A rapid and simple diversity-oriented synthesis ofnovel 3-amino-2’-oxospiro[benzo[c]pyrano[3,2-a]phenazine-1,3’-indoline]-2-carbonitrile/carboxylatederivatives via a one-pot, four-component domino reaction. // Tetrahedron Lett. – 2013. – Vol. 54. – P.3487–3492.79Jin Sh.-sh., Guo H.-yu. Solvent-free and ionic liquid catalysed three-component methodsynthesis of spiro-2-amino-4H-pyrans derivatives. // J. Chem. Res.
– 2012. – P. 638-640.80Saeedi M., Heravi M.M., Beheshtiha Ya.S., Oskooie H.A. One-pot three-component synthesis of thespiroacenaphthylene derivatives. // Tetrahedron. – 2010. – Vol. 66. – P. 5345-5348.11781Mohammadi Ziarani G., Hajiabbasi P., Badiei A., Amanlou M. Facile one-pot synthesis ofspiroacenaphthylene derivatives using SBA-Pr-NH2. // J. Chil. Chem. Soc. – 2015.
– Vol. 60. – No. 2. –P. 2914-2918.82Medvedeva S.M., Sabynin A.L., Shikhaliev Kh.S. Efficient methods for the synthesis ofspiroheterocyclic systems based on 4,4,6-trimethyl-4H-pyrrolo[3,2,1-ij]quinoline-1,2-diones. // Russ.Chem. Bull. Int. Ed. – 2014. Vol.63. – No. 12. – P. 2693-2701.83Esquivias-Pérez M., Maalej E., Romero A., Chabchoub F., Samadi A., Marco-Contelles J. María JesúsOset-Gasque M.J.
Nontoxic and neuroprotective β‑naphthotacrines for Alzheimer’s disease. // Chem.Res. Toxicol. – 2013. – Vol. 26. – P. 986−992.84Gong H., Yang M., Xiao Z., Doweyko A.M., Cunningham M., Wang J., Habte S., Holloway D., BurkeCh., Shuster D., Gao L., Carman J., Somerville J.E., Nadler S.G., Salter-Cid L., Barrish J.C., WeinsteinD.S. Discovery of acylurea isosteres of 2-acylaminothiadiazole in the azaxanthene series ofglucocorticoid receptor agonists. // Bioorg. Med. Chem.
Lett. – 2014. – Vol. 24. – P. 3268–3273.85Kanakaraju S., Prasanna B., Basavoju S., Chandramouli G.V.P. Ionic liquid catalyzed one-pot multi-component synthesis, characterization and antibacterial activity of novel chromeno[2,3-d]pyrimidin-8amine derivatives. // J. Mol. Struct. – 2012. – Vol. 1017. – P.
60–64.86Khoobi M., Ramazani A., Hojjati., Shakeri R., Khoshneviszadeh M., Ardestani S.., Shafiee A.,Foroumadi A., Joo S.W. Synthesis of novel 4H-chromenes containing a pyrimidine-2-thione function inthe presence of Fe3O4 magnetic nanoparticles and study of their antioxidant activity. // Phosphorus,Sulfur Silicon Relat.
Elem. – 2014. – Vol. 189. – P. 1-10.87Осянин В.А., Осипов Д.В., Климочкин Ю.Н. Синтез 9,11-диамино-12H-бензо[5,6]хромено[2,3-b]пиридин-10-карбонитрилов. // ХГС. – 2011. – № 11. – С. 1750-1752.88Elinson M.N., Gorbunov S.V., Vereshchagin A.N., Nasybullin R.F., Goloveshkin A.S., BushmarinovI.S., Egorov M.P. Chemical and electrocatalytic cascade cyclization of salicylaldehyde with threemolecules of malononitrile: ‘one-pot’ simple and efficient way to the chromeno[2,3-b]pyridine scaffold.// Tetrahedron. – 2014. – Vol.
70. – P. 8559-8563.89Olyaei A., Vaziri M., Razeghi R. A one-pot, pseudo four-component synthesis of novelbenzopyrano[2,3-b]pyridines under solvent-free conditions. // Tetrahedron Lett. – 2013. – Vol. 54. – P.1963–1966.90Vereshchagin A.N., Elinson M.N., Anisina Yu.E., Ryzhkov F.V., Goloveshkin A.S., BushmarinovI.S., Zlotin S.G., Egorov M.P. Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5Hchromeno[2,3-b]pyridine scaffold. // Mendeleev Commun. – 2015. – Vol. 25. – P. 424–426.91Mishra S., Ghosh R. K2CO3-Mediated, one-pot, multicomponent synthesis of medicinally potentpyridine and chromeno[2,3-b]pyridine scaffolds.
// Synth. Commun. – 2012. – Vol. 42. – P. 2229–2244.11892Banerjee S., Wang J., Pfeffer S., Ma D., Pfeffer L.M., Patil S.A., Li W., Miller D.D. Design, synthesisand biological evaluation of novel 5H-chromenopyridines as potential anti-cancer agents. // Molecules.– 2015. – Vol. 20. – P. 17152-17165.93Safaei-Ghomi J., Kiani M., Ziarati A., Shahbazi-Alavi H. Highly efficient synthesis ofbenzopyranopyridines via ZrP2O7 nanoparticles catalyzed multicomponent reactions of salicylaldehydeswith malononitrile and thiols.
// J. Sulfur Chem. – 2014. – Vol. 35. – No. 4. – P. 450–457.94Damavandi S., Sandaroos R. Bis(imino)pyridine (BIMP) Fe(II) catalyses one-pot green condensationof resorcinol, malononitrile, aromatic aldehydes and cyclohexanone. // J. Chem. Sci. – 2012. – Vol. 124.– No. 2. – P. 483–486.95Damavandi S. Direct, facile, eco-friendly, and four-component synthesis of pyranopyridinederivatives. Synth. React.
Inorg. Met.-Org. Nano-Met. Chem. – 2012. – Vol. 42. – P. 1251–1254.96Wu H., Lin W., Wan Yu, Xin H.., Shi D., Shi Ya., Yuan R., Bo R., Yin W. Silica gel-catalyzed one-pot syntheses in water and fluorescence properties studies of 5-amino-2-aryl-3H-chromeno[4,3,2de][1,6]naphthyridine-4-carbonitriles and 5-amino-2-aryl-3H-quinolino[4,3,2-de][1,6]naphthyridine-4carbonitriles. // J.
Comb. Chem. – 2010. – Vol. 12. – P. 31–34.97Rajanarendar E., Ramakrishna S., Kishore B. A Convenient and facile synthesis of isoxazolyl-chromeno[4,3,2-de]pyrimido[4,5-h][1,6]napthyridinones. // J. Heterocyclic Chem. – 2014. – Vol. 51. –P. 1415-1420.98Ghahremanzadeh R., Amanpour T., Bazgir A. Pseudo four-component synthesis ofbenzopyranopyrimidines. // Tetrahedron Lett. – 2012. – Vol. 51. – P. 4202–4204.99Tavakoli H.R., Moosavi S.M., Bazgir A. ZrOCl2·8H2O as an efficient catalyst for the pseudo four-component synthesis of benzopyranopyrimidines. // J.
Korean Chem. Soc. – 2013. – Vol. 57. – No. 2. –P. 260-263.100Heravi M.M., Zakeri M. Use of sodium molybdate dihydrate as an efficient heterogeneous catalystfor the synthesis of benzopyranopyrimidine derivatives. // Synth. React. Inorg. Met.-Org. Nano-Met.Chem.
– 2013. – Vol. 43. – P. 211–216.101Amirnejat S., Movahedi F., Masrouri H., Mohadesi M., Kassaee M.Z. Silica nanoparticlesimmobilized benzoylthiourea ferrous complex as an efficient and reusable catalyst for one-pot synthesisof benzopyranopyrimidines. // J. Mol.
Catal. A: Chem. – 2013. – Vol. 378. – P. 135-141.102Gupta A.K., Kumari K., Singh N., Raghuvanshi D.S., Singh K.N. An eco-safe approach tobenzopyranopyrimidines and 4H-chromenes in ionic liquid at room temperature. // Tetrahedron Lett. –2012. – Vol. 53. – P. 650–653.103Shaterian H. R., Aghakhanizadeh M. Mild preparation of chromeno[2,3-d]pyrimidinescatalyzed by Brønsted acidic ionic liquids under solvent-free and ambient conditions.
// Res. Chem.Intermed. – 2013. – Vol. 39. – P. 3877–3885.119104Zonouzi A., Biniaz M., Mirzazadeh R., Talebi M., Ng S.W. An efficient one-pot and solvent-freesynthesis of chromeno[2,3-d]pyrimidine derivatives: microwave assisted reaction. // Heterocycles. –2010. – Vol. 81. – No.