Диссертация (1173073), страница 14
Текст из файла (страница 14)
–№ 5. – P. 868-970.2. Scott M.K. Piperazinylalkyl heterocycles as potential antipsychotic agents /M.K.Scott, E.W.Baxter, D.J.Bennett, R.E.Boyd, P.S.Blum, E.E.Codd, M.J.Kukla,E.Malloy, B.E.Maryanoff, C.A.Maryanoff, M.E.Ortegon, C.R.Rasmussen, A.B.Reitz,M.J.Renzi, C.F.Schwender, R.P.Shank, R.G.Sherrill, J.L.Vaught, F.J.Villani, N.Yim //J. Med. Chem. – 1995. – Vol.
38. – P. 4198-4210.3. Патент США US 4216221. 1,3-disubstituted (2-thio)ureas / De Lannoy J. –опубл. 5.08.1980.4. Патент WO2005054188A1. Imidazole derivatives, processes for preparingthem and their uses / Kenda B., Michel P., Quesnel Y. – опубл. 16.06.2005.5. Патент США US3073843.
Preparation of N-hydroxymethyl pyrrolidone / BucS. – опубл. 15.01.1963.6. Патент США US4769454. Process for the preparation of N-methylolcaprolactam / Blank H.-U., Bauer W. – опубл. 06.09.1988.7. Joubert F. Preparation, properties, and antibacterial behavior of a novelcellulose derivative containing lactam groups / F.Joubert, G.J.Sharples, O.M.Musa,D.R.W.Hodgson, N.R.Cameron // Journal of polymer science, part A: polymerchemistry. – 2015. – Vol.
53. – P. 68-78.8. Jouglet B. An efficient hydroxymethylation of lactams / B.Jouglet, S.Oumoch,G.Rousseau // Synth. Comm. – 1995. – Vol. 25(23). – P. 3869-3874.9. Mahfouz N. Cyclic amide derivatives as potential prodrugs II: Nhydroxymethylsuccinimide- / isatin esters of some NSAIDs as prodrugs with animproved therapeutic index / N.M.Mahfouz, F.A.Omar, T.Aboul-Fadl // Eur.
J. Med.Chem. – 1999. – Vol. 34. – P. 551-562.10. Cherbuliez E. Dérivés formaldéhydiques de la succinimide / E.Cherbuliez,G.Sulzer // Helv. Chim. Acta. – 1925. – Vol. 8. – P. 567-571.10211. Патент США US2526517. N-methylol maleimide / Tawney P. O. – опубл.17.10.1950.12. Sachs F.
Eine Condensation von Phtalimid mit Formaldehyd / F.Sachs //Chem. Ber. – 1898. – P. 3230-3235.13. Sachs F. Ueber die Bromirung alkylirter Phtalimide und einige Derivative desMethylphtalimids / F.Sachs // Chem. Ber. – 1898. – P. 1225-1233.14. Sakellarios E. J. Purification of N-hydroxymethylphthalimide through amolecular compound with pyridine / E.J.Sakellarios // J. Am. Chem. Soc.
– 1948. – Vol.70. – P. 2822.15. Zaugg H. α-Amidoalkylations at carbon / H.Zaugg, W.Martin. – NY.: JohnWiley & Sons. – 1965. – 167 p.16. Aboul-Fadl T. Synthesis, Antitubercular Activity and PharmacokineticStudies of Some Schiff Bases Derived from 1- Alkylisatin and Isonicotinic AcidHydrazide (INH) / T.Aboul-Fadl, F.A.-H.Mohammed, E.A.-S.Hassan // Arch. Pharm.Res. – 2003.
– Vol. 26 № 10. – P. 778-784.17. Reißert A. Über die Einwirkung von Formaldehyd auf formyliertearomatische Amine und auf Isatin / A.Reißert, A.Haendler // Chem. Ber. – 1924. Vol.57. – P. 989-996.18. Böhme H. Über Darstellung und Umsetzungen von N-(α-Hydroxy-β,β,βtrichlor-äthyl)-carbonsäureamiden und N-(α,β,β,β-Tetrachlor-äthyl)-carbonsäureamiden/ H.Böhme, F.Eiden, D.Schünemann // Archiv der Pharmazie.
– 1961. – Vol. 294. – P.307-311.19.pyrrolidonesПатентandСШАaUS2924606.processfortheN-alpha-hydroxy-beta-trihalogenethyl)productionofN-alpha-hydroxy-beta-trihalogenethyl)-pyrrolidones / Schroeder H., Amann A. – опубл. 09.02.1960.20.ПатентСШАUS3253030.N-2-trichloro-1-hydroxymethyl-N’-2-hydroxyethyl formamide / Buc S. – опубл. 24.05.1966.21. Vail S. The formation of N,N'-dihydroxyethylenehisamides from glyoxal andselected amides / S.Vail, C.Moran, H.Barker // J.
Org. Chem. – 1965. – Vol. 30. – P.1195-1199.10322. Патент США US3579536A. Addition products of methylformamide orsuccinimide with glyoxal / Vail S., Pierce A. – опубл. 18.05.1971.23. Патент США US3627476. Amide-glyoxal addition products and their use ascrosslinking agents / Vail S., Pierce A. – опубл. 14.12.1971.24. Vail S.
Limitations for the addition of amides to formaldehyde and glyoxal /S.Vail, A.Pierce // J. Org. Chem. – 1972. – Vol. 37. – P. 391-393.25. Sizova E. V. Derivatives of 1,1,2,2-tetraaminoethane: I. Condensation of 1,2diacetoxy-1,2-bis(acylamino)ethaneswithnitrogen-containingnucleophiles/E.V.Sizova, V.V.Sizov, M.P.Zelenov, I.V.Tselinskii // Russian Journal of organicchemistry. – 2007. Vol. 43 № 2.
– P. 178-183.26. Majumdar S. α-(1H-Imidazol-1-yl)alkyl (IMIDA) carboxylic acid esters asprodrugs of carboxylic acid containing drugs / S.Majumdar, M.M.Spaeth, S.Sivendran,J.Juntunen, J.D.Thomas, K.B.Sloan // Tetrahedron Letters. – 2007. – Vol. 48. – P. 46094611.27. Elguero J. A selective synthesis of unsymmetrical 1,1’-methylenebisdiazolesby solid-liquid phase transfer catalysis / S.Juliá, C.Martínez-Martonell, J.Elguero //Heterocycles. – 1986. – Vol.
24 № 8. – P. 2233-2237.28. Katritzky A. The Chemistry of N-Substituted Benzotriazoles. Part 2.Reactions of Benzotriazole with Aldehydes and Aldehyde Derivatives. 1-(αHydroxyalkyl)-, 1-(α- Alkoxyalkyl) -, and 1-(α-Acyloxyalkyl)benzotriazoles /A.R.Katritzky, S.Rachwal, B. Rachwal // J.
Chem. Soc. Perkin Trans. I. – 1987. – P.791-797.29. Katritzky A. Benzotriazole mediated synthesis of methylenebisanilines /A.R.Katritzky, X.Lan, J.N.Lam // Synthesis. – 1990. – P. 341-346.30. Katritzky A. N-[α-(o- and p-Methoxyary1)alkyl]benzotriazoles: preparationand use in synthesis / A.R.Katritzky, X.Lan, J.N.Lam // Chem. Ber. – 1991. – Vol. 124.– P. 1819-1826.31. Katritzky A. An NMR study of the equilibria involved with benzotriazole,carbonyl compounds, and their adducts / A.R.Katritzky, S.Perumal, G.P.Savage // J.Chem. Soc. Perkin Trans. II.
– 1990. – P. 921-924.10432. Alkorta I. Study of the structure of 1-hydroxymethylindazole and 1hydroxymethylbenzotriazole by X-ray crystallography, multinuclear NMR in solutionand DFT calculations / I.Alkorta, J.Elguero, N.Jagerovic // J. Heterocyclic Chem. –2004. – Vol. 41. – P. 285-289.33.ПатентГерманииDE256757.VerfahrenzurDarstellungvonMethylolcarbazol / M.Lange – опубл. 20.02.1913.34. Miyata N. Oxidative dealkylation of tertiary amines by iron(III) porphyriniodosoxylene system as a model of cytochrome P-450 / N.Miyata, H.Kiuchi, M.Hirobe// Chem. Pharm.
Bull. – 1981. – Vol. 29 № 5. – P. 1489-1492.35. Bamberger E. Producte der Addition von Chloral an Chinolinbasen undBenzimidazole / E.Bamberger, B.Berlé // Annalen. – 1893. – Vol. 273 № 2-3. – P.364373.36. Teichmann B. Zur Reaktion von Chloral mit Benztriazolen / B.Teichmann //Zeitschrift für Chemie. – 1964. – Vol. 4 № 6. – P. 230.37. Getz J. Mechanism of hydrolysis of O-imidomethyl derivatives of phenols /J.J.Getz, R.J.Prankerd, K.B.Sloan // J. Org.
Chem. – 1993. – Vol. 58. – P. 4913-4918.38. Böhme H. Über Imidomethyl-thiokohlensäure- ester / H.Böhme, H.-H.Otto //Archiv der Pharmazie. – 1967. – Vol. 300 № 11. – P. 922-925.39. Liu W. All-in-One: achieving robust, strongly luminescent and highlydispersible hybrid materials by combining ionic and coordinate bonds in molecularcrystals / W.Liu, S.J.Teat, G.Dey, Z.Shen, L.Wang, D.M.O’Carroll, J.Li // J. Am.Chem. Soc. – 2017. – Vol.
139. – P. 9281-9290.40.ШиповиспользованиемА.Г.системыОдностадийныйсинтезN-хлорметиллактамовпараформ-триметилхлорсилан/сА.Г.Шипов,Н.А.Орлова, Ю.И.Бауков // Журнал общей химии. – 1984. – т. 54. – Вып. 11. – С.2645-2646.41. Bugaev I. M. Direct phthalimidomethylation of 2,6-dialkylphenols. Reactionsof N-(4-hydroxybenzyl)phthalimides with electrophiles and nucleophiles / I.M.Bugaev,A.I.Dmitriev, A.E.Prosenko // Russ. Chem. Bull. – 2012.
– Vol. 61 № 2. – P. 298-302.10542.ПатентГерманииDЕ134979.VerfahrenzurDarstellungvonBenzylphtalimiden / J.Tscherniac – опубл. 10.10.1902.43. Einhorn A. Über die N-Methylolverbindungen der Säureamide / A.Einhorn,T.Mauermayer, C.Ladisch, G.Schupp // Annalen. – 1905. – P.
207-305.44. Zaugg H. The Tscherniac-Einhorn reaction. I. Equilibria in solutions of Nhydroxymethylphtalimide in strong sulfuric acid / H.E.Zaugg, A.M.Kotre, J.E.Fraser //J. Org. Chem. – 1969. – Vol. 34 № 1. – P. 11-13.45. Zaugg H. The Tscherniac-Einhorn reaction. II. Kinetics and mechanism /H.E.Zaugg, R.W.DeNet, J.E.Fraser, A.M.Kotre // J.
Org. Chem. – 1969. – Vol. 34 № 1.– P. 14-18.46. Hess F. A facile route for the preparation of 4-aminomethylacridine and itsderivatives / F.Hess, E.Cullen, K.Grozinger // Tetrahedron Letters. – 1971. – Vol. 28. –P. 2591-2594.47. Ben-Ishai D. The amidoalkylation of aromatics compounds and olefins with5-alkoxyhydantoins / D.Ben-Ishai, G.Ben-Ishai // J. Heterocyclic Chem. – 1970.
– Vol.7. – P.1289-1293.48. Ben-Ishai D. A new synthesis of N-acyl aromatic α-amino acidsamidoalkylation of aromatic and heterocyclic compounds with glyoxylic acidderivatives / D.Ben-Ishai, J.Sataty, Z.Bernstein // Tetrahedron. – 1976. – Vol. 32. – P.1571-1573.49. Barry J. The amidoalkylation of aromatic hydrocarbons / J.Barry, E.Mayeda,S.Ross // Tetrahedron.
– 1976. – Vol. 33. – P. 369-372.50. Патент Великобритании GB1547333A. Preparation of polycarbonates usingphenols amidoalkylated in the 4-position as chain-breaking agents / Idel K. J., MeyerR.-V., Fengler G., Michael D. – опубл. 13.06.1976.51. Venkov A. Synthesis of 1-Phenyl-2-acyl-tetrahydroisoquinolines byIntermolecular α-Amidoalkylation Reaction / A.Venkov, S.Statkova, I.Ivanov //Synthetic Communication.
– 1992. – Vol. 22. – P. 125-134.52.AizinaYu.N-(2,2,2-Trichloroethylidene)-andN-(1-Hydroxy-2,2,2-trichloroethyl) amides in C-Amidoalkylation Reaction of Functionally-substituted106Aromatic Compounds / Yu.Aizina, I.Rozentsweig, A.Mirskova // Russian Journal ofOrganic Chemistry. – 2001. – Vol. 38.
– P. 235-238.53. Zaugg H. α-Amidoalkylation at carbon: recent advances – part I / H.E.Zaugg// Synthesis. – 1984. – P. 85-110.54. Патент США US3829528. Method of producing resorcinol resins by reactingwith N-methylol caprolactam / Aarna A.Y., Kiisler K.R., Kristyanson P.G., TannerJ.A.-M. – опубл. 13.08.1974.55. Christjanson P. Co-Condensates of resorcinols and methylol compounds foradhesive resins / P.Christjanson, A.Köösel, K.Siimer, A.Suurpere // Polymerengineering and science.