Диссертация (1150220), страница 28
Текст из файла (страница 28)
Beveridge, R.A. Batey // Org. Lett. –2012. – Vol. 14. – № 2. – P. 540-543.45.Coutouli-Argyropoulou,E.ThermalDecompositionofSilverSaltsofAryldinitromethanes in the Presence of Unsaturated Systems. Possible Formation ofArylnitrocarbenes / E. Coutouli-Argyropoulou, N.E.
Alexandrou // J. Org. Chem. –1980. – Vol. 45. – P. 4158-4162.46.Lasri, J. Efficient Regioselective Synthesis of 4- and 5-Substituted Isoxazoles underThermal and Microwave Conditions / J. Lasri, S. Mukhopadhyay, M.A.J. Charmier // J.Heterocyclic Chem. – 2008. – Vol. 45. – P. 1385-1389.47.Saad, A.
One Step Regioselective Synthesis of 5-Aminoisoxazoles from Nitrile Oxidesand α-Cyanoenamines / A. Saad, M. Vaultier, A. Derdour // Molecules. – 2004. – Vol.9. – P. 527-534.48.Rajagopalan, P. Dipolar addition reactions of nitriloxides. IV. The cycloaddition ofnitriloxides to ketene aminals / P.
Rajagopalan, O.N. Talaty // Tetrahedron Lett. – 1966.– № 38. – P. 4537-4539.49.Volkova,Y.A.UnexpectedHeterocyclizationofElectrophilicAlkenesbyTetranitromethane in the Presence of Triethylamine. Synthesis of 3-Nitroisoxazoles /Y.A. Volkova, E.B. Averina, Y.K. Grishin, P. Bruheim, T.S. Kuznetsova, N.S. Zefirov// J. Org.
Chem. – 2010. – Vol. 75. – P. 3047-3052.50.Averina, E.B. Heterocyclization of electrophilic alkenes with tetranitromethanerevisited: regiochemistry and the mechanism of nitroisoxazole formation / E. B.Averina, Y. V. Samoilichenko, Y. A. Volkova, Y. K. Grishin, V. B. Rybakov, A. G.Kutateladze, M. E. Elyashberg, T. S. Kuznetsova, N. S. Zefirov // Tetrahedron Lett. –2012. – Vol. 53. – № 12. – P. 1472-1475.51.Averina, E.B. Chemoselective Reduction of Functionalized 5-Nitroisoxazoles:Synthesis5-Amino-and5-[Hydroxy(tetrahydrofuran-2-yl)amino]isoxazoles177/E.B.
Averina, D.A. Vasilenko, Y.V. Samoilichenko, Y.K. Grishin, V.B. Rybaka, T.S.Kuznetsova, N.S. Zefirov // Synthesis. – 2014. – Vol. 46. – P. 1107-1113.52.Zhang, M.X. Nitroacetylene: HC≡CNO2 / M.X. Zhang, P.E. Eaton, I. Steele, R. Gilardi// Synthesis. – 2002. - № 14. – P. 2013-2018.53.Johnson, L. A Reliable Synthesis of 3-Amino-5-Alkyl and 5-Amino-3-Alkyl Isoxazoles/ L. Johnson, J. Powers, F.
Ma, K. Jendza, B. Wang, E. Meredith, N. Mainolfi //Synthesis – 2013. – Vol. 45. – P. 171-173.54.Li, X. Synthesis and Biological Evaluation of Chromenylurea and ChromanylureaDerivatives as Anti-TNF-α agents that Target the p38 MAPK Pathway / X. Li, X. Zhou,J. Zhang, L. Long, Z. Zheng, S. Li, W. Zhong // Molecules. – 2014. – Vol. 19. – P.2004-2028.55.Rowbottom, M.W. Identification of 1-(3-(6,7-Dimethoxyquinazolin-4-yloxy)phenyl)-3(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)ureaHydrochloride(CEP-32496), a Highly Potent and Orally Efficacious Inhibitor of V-RAF Murine SarcomaViral Oncogene Homologue B1 (BRAF) V600E / M.W.
Rowbottom et al. // J. Med.Chem. – 2012. – Vol. 55. – P. 1082-1105.56.Bai,J.R.Synthesisandbiologicalevaluationof4’-[(benzimidazole-1-yl)methyl]biphenyl-2-sulfonamide derivatives as dual antiotensin II/endothelin Areceptor antagonists / J. R. Bai, Z. Wei, J. Liu, W. Xie, H. Yao, X. Wu, J. Jing, Q.Wang, J. Xu // Bioorg. Med. Chem. – 2012.
– Vol. 20. – P. 4661-4667.57.Eddington, N.D. Synthesis and anticonvulsant activity of enaminones. 4. Investigationson isoxazoles derivatives / N.D. Eddington et al. // Eur. J. Med. Chem. – 2002. – Vol.37. – P. 635-648.58.Kong, Y.C. A modified procedure for the synthesis of 5-amino-3-arylisoxazoles andtheirreactionswithtetrasulfurtetranitrideantimony(V)chloridecomplex(S4N4·SbCl5): novel synthesis of 3-aryl-1,2,5-thiadiazole-4-carboxamides / Y.C. Kong,K. Kim, Y.J. Park // Heterocycles. – 2001.
– Vol. 55. – № 1. P. 75-89.59.Mohareb, R.M. α-Haloketoximes in Heterocyclic Synthesis: Polyfunctional Azoles andAzines from α-Bromo ketoximes / R.M. Mohareb, A. Habashi, E.A.A. Hafez, S.M.Sherif // Arch. Pharm. (Weinhem). – 1987. – Vol. 320. – P. 776-780.17860.Ohno, M. Reaction of 2-Chlorocycloalkanone Oximes. II. Syntheses of 3Aminocycloalka[C]isoxazoles /M. Ohno, N.
Naruse // Bull. Chem. Soc. Jpn. – 1966. –Vol. 39 – P. 1125-1128.61.Dines, M. A two-step synthesis of 5-aminoisoxazoles from olefins / M. Dines, M.L.Scheinbaum // Tetrahedron Lett. – 1969. – № 54. – P. 4817-4819.62.Lesiv, A.V. Reactions of N,N-bis(siloxy)enamines with trimethylsilyl cyanide: aliphaticnitro compounds as convenient precursors of 5-aminoisoxazoles / A.V. Lesiv, S.L.Ioffe, Y.A. Strelenko, I.V. Bliznets, V.A. Tartakovsky // Mendeleev Commun. – 2002.– Vol. 12. – № 3.
– P. 99-102.63.Navarro-Ocaña, A. Synthesis of Substituted Isoxazoles from (Z)-3-Alkyl-3-Nitro-2Phenylpropenenitriles using Baker’s Yeast / A. Navarro-Ocaña, M. Jimēnez-Estrada,M.B. González-Parades, E. Bárzana // Synlett. – 1996. – P. 695-696.64.Forum, Z.T. Allenes.
Part 42. Nucleophilic Addition of Hydroxylamine to Allenic andAcetylenic Nitriles; Synthesis of 3-Alkyl-5-amino, 5-Amino-3-phenyl-, and 3-Amino-5phenyl-isoxazoles / Z.T. Forum, P.F. Asobo, S.R. Lanbor, P.D. Landor // J. Chem. Soc.Perkin Trans. 1.
– 1984. – P. 1079-1083.65.Petrosyan, V.A. Reactions of 3-cyclopropyl-3-oxopropionitrile anion generated byelectroreduction of 5-cyclopropylisoxazole / V.A. Petrosyan, S.V. Neverov, V.L.Sigacheva // Russ. Chem. Bull. Int. Ed. – 2007. – Vol. 56. – № 11. – P. 2184-2188.66.Vogl, E. A new bactericidal lead structure for the protection of materials / E.
Vogl, R.Bruns, O. Kretschik, H. Uhr, J. Kaulen, M. Kugler, P. Wachtler, W. Kreiss, G. Eberz //Bioorg. Med. Chem. Lett. – 2005. – Vol. 15. – P. 625-629.67.Magar, B.K. Synthesis and Antimicrobial Activity of Isoxazoles / B.K. Magar, V.N.Bhosale, B.N. Berard // Der Chemica Sinica. – 2011. - № 5. – P. 147-151.68.Alberola, A.
Reduction of 4-Cyanoisoxazoles with Lithium Aluminium Hydride.Synthesis of 5-Aminoisoxazoles / A.Alberola, A.M. González, M.A. Laguna, F.J.Pulido // J. Org. Chem. – 1984. – Vol. 49. – P. 3423-3424.69.He, Y. Synthesis and SAR of novel isoxazoles as potent c-jun N-terminal kinase (JNK)inhibitors / Y.
He et al. // Bioorg. Med. Chem. Lett. – 2014. – Vol. 24. – P. 161-164.70.Dondoni, A. A new Convenient Preparathion of 2-, 4-, and 5-Thiazolecarboxaldehydesand Their Conversion into the Corresponding Carbonitrile N-Oxides: Synthesis of 3-179Thiazolylisoxazoles and 3-Thiazolylisoxazolines / A. Dondoni, G. Fantin, M.Fogagnolo, A. Medici, P. Perdini // Synthesis. – 1987. – P. 998-1001.71.Moriya, O. Synthesis of isoxazolines and isoxazoles from aldoximes by the use ofsodium bromite with organotin halide / O. Moriya, H. Nakamura, T. Kageyama, Y.Urata // Tetrahedron Lett.
– 1989. – Vol. 30. – № 30. – P. 3987-3990.72.Gómez-Galeno, J. A Potent and Selective AMPK Activator That Inhibits de NovoLipogenesis / J. Gómez-Galeno et al. // ACS Med. Chem. Lett. – 2010. – Vol. 1. – P.478-482.73.Kozikowski, A.P. A Nitrile Oxide Based Entry to 2,3-Dihydropyran-4-ones. Synthesisof a Protected Version of “Compactin Lactone” in Racemic and Optically Active Forms/ A.P. Kozikowski, C.-S. Li // J. Org. Chem. – 1985.
– Vol. 50 – P. 778-785.74.Hertenstein, U. Enolester von Acylcyaniden: Synthesen und allgemeine Eigenschaften /U. Hertenstein, S. Hünig, H. Reichelt, R. Schaller // Chem. Ber. – 1986. – Vol. 119. – P.699-721.75.Ismailov, V.M. Synthesis of New Isoxazole Derivatives / V.M. Ismailov, M.M.Kantaeva, I.A. Mamedov, N.N. Yusubov // Russ. J. Org. Chem. – 2004. – Vol. 40.
– №12. – P. 1826-1827.76.Laufer, S.A. Isoxazolone Based Inhibitors of p38 MAP Kinases / S. A. Laufer, S.Margutti // J. Med. Chem. – 2008. – Vol. 51. – P. 2580-2584.77.Grigg, R. Pd(0) catalyzed three-five-component C-2-arylallylation of active methyleneheterocycles: pyrazolones, oxazolones, isoxazolones and N,N’-dimethylbarbituric acid /R. Grigg, M. R. A. Sarkar, A. Thayapan, V. Sridharan, C.
W.G. Fishwick //Tetrahedron. – 2007. – Vol. 63. – P. 7213-7228.78.Micetich, R.G. Studies in isoxazoles chemistry. III. The preparation and lithiation of3,5-disubstituted isoxazoles / R.G. Micetich, C.G. Chin // Can. J. Chem. – 1970. – Vol.48. - № 9. – P. 1371-1376.79.Álvares, Y.S.R. Diastereoselective synthesis of aziridines from (1R)-10-(N,Ndialkylsulfamoyl)isobornyl-2H-azirine-3-carboxylates / Y.S.R.
Álvares, M.J. Alves,N.G. Azoia, J.F. Bickley, T.L. Gilchrist // J. Chem. Soc. Perkin Trans. 1 – 2002. – P.1911-1919.18080.Davis, F.A. Aziridine-mediated asymmetric synthesis of quaternary β-amino acidesusing 2H-azirine 2-carboxylate esters / F.A. Davis, J. Deng, Y. Zhang, R.C.Heltiwanger // Tetrahedron, 2002, 58, 7135-7143.81.Sakai, T. Lipase-Catalysed Resolution of (2R*,3S*)- and (2R*,3R*)-3-Methyl-3phenyl-2-aziridinemethanol at Low Temperatures and Determination of the AbsoluteConfigurations of the Four Stereoisomers / T. Sakai, Y. Liu, H.
Ohta, T. Korenaga, T.Ema // J. Org. Chem. – 2005. – Vol. 70. – P. 1369-1375.82.Palacios, F. Reaction of 2H-Azirine Phosphine Oxide and –Phosphonates withNucleophiles. Stereoselective Synthesis of Functionalized Aziridines and α- and βAminophosphorus Derivatives / F. Palacios, A.M. Ochoa de Retana, J.M. Alonso //J.Org. Chem. – 2005. – Vol. 70. – P. 8895-8901.83.Banert, K. Synthesis and Reactions of Highly Strained 2,3-Bridged 2H-Azirines / K.Banert, B. Meier // Angew. Chem. Int. Ed. – 2006.
– Vol. 45. – P. 4015-4019.84.Tsuritani, T. Base-Induced Condensation of α-Chloro Oxime Derivatives FurnishesAlkynes / T. Tsuritani, K, Yagi, H. Shinokubo, K. Oshima // Angew. Chem. Int. Ed. –2003. – Vol. 42. – P. 5613-5615.85.Sato, S. Some Reactions of Phenylazirine / S. Sato, H. Kato, M. Ohta // Bull Chem SocJpn. – 1967.
– Vol. 40. – № 4. – P. 1014.86.Sato, S. Azirines. I. The Reaction of 2-Phenylazirine with Carbanions / S. Sato, H.Kato, M. Ohta // Bull Chem Soc Jpn. – 1967. – Vol. 40. – № 12. – P. 2936-2938.87.Laurent, A. Synthese de 2H-pyrroles et de pyrroles: action de carbanions sur de N,N,Ntrimethylhydrazonium / A. Laurent, P.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
