Диссертация (1150310), страница 26
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– Vol. 46. – P. 15–18.33. Díez-González, S. N-heterocyclic carbenes in late transition metal catalysis / S. DíezGonzález, N. Marion, S. P. Nolan // Chem. Rev. – 2009. – Vol. 109. – P. 3612−3676.34. Szulmanowicz, M. S. Structure, dynamics and catalytic activity of palladium(II)complexes with imidazole ligands / M. S. Szulmanowicz, W. Zawartka, A. Gniewek,A. M.
Trzeciak // Inorganica Chimica Acta. – 2010. – Vol. 363. – P. 4346-4354.35. Kuznetsov, M. A. Oxidative aminoaziridination: past, present, and future / M. A.Kuznetsov, L. M. Kuznetsova, A. S. Pankova // Tetrahedron Lett. – 2016. – Vol. 57. –P. 3575–3585.36. Langille, N. F. Sonogashira coupling of functionalized trifloyl oxazoles and thiazoleswith terminal alkynes: synthesis of disubstituted heterocycles / N. F. Langille, L. A.Dakin, J. S.
Panek // Org. Lett. – 2002. – Vol. 4. – P. 2485–2488.37. Counceller, C. M. Synthesis of 2,4- and 2,5-Disubstituted Oxazoles via MetalCatalyzed Cross-Coupling Reactions / C. M. Counceller, C. C. Eichman, N. Proust, J.P. Stambuli // Adv. Synth. Catal. – 2011. – Vol. 353. – P. 79–83.38. Walton, D. R. M. Friedel-Сrafts reactions of bis(trimethylsilyl)polyynes with acylchlorides; a useful route to terminal-alkynyl ketones / D. R. M. Walton, F. Waugh // J.Organomet. Chem.
– 1972. – Vol. 37. – P. 45–46.14839. Iso, Y. Synthesis of 4-arylethynyl-2-methyloxazole derivatives as mGluR5antagonists for use in the treatment of drug abuse / Y. Iso, A. P. Kozikowski //Synthesis. – 2006. – Vol. 2. – P. 243–246.40. Smith, C. D. Synthesis of linked heterocycles via use of bis-acetylenic compounds /C. D. Smith, K. Tchabanenko, R. M. Adlington, J. E. Baldwin // Tetrahedron Lett.
–2006. – Vol. 47. – P. 3209–3212.41. Wang, Y. A novel and efficient synthesis of terminal arylacetylenes via Sonogashiracoupling reactions catalysed by MCM-41-supported bidentate phosphine palladium(0)complex / Y. Wang, B. Huang, S. Sheng, M. Cai // J. Chem. Res. – 2007. – Vol. 2007.– P. 728-732.42. Белецкий,Е.В.ОкислительноеприсоединениеN-аминофталимидакфталоилгидразону коричного альдегида / Е.В. Белецкий, М.А. Кузнецов //ЖОрХ.
– 2009. – T. 45. – C. 804-805.43. Pankova, A. S. Synthesis of 2-(Hetero) aryl-5-(trimethylsilylethynyl) oxazoles from(Hetero) arylacrylic Acids / A. S. Pankova, A. Yu. Stukalov, M. A. Kuznetsov // Org.Lett. – 2015. – Vol. 17. – P. 1826–1829.44. Stukalov, A. Pyrazoles and C-Imidoylaziridines through [4+1] Annulation and [2+1]Cycloadditionof1-Azabuta-1,3-dieneswithaSyntheticEquivalentofPhthalimidonitrene / A. Stukalov, V.
V. Sokolov, V. V. Suslonov, M. A. Kuznetsov //Eur. J. Org. Chem. – 2017. – Vol. 2017. – P. 2587–2595.45. Stukalov, A. Thermal Ring Expansion of 2-Sulfonylimidoyl-1-phthalimidoaziridinesinto N-Sulfonylimidazoles / A. Stukalov, V.V.Suslonov, М.А.Кuznetsov // Eur. J.Org. Chem. – 2018. – DOI: 10.1002/ejoc.201701806.46. Whitlock, H.W. Jr. The rearrangement of an N-vinylaziridine / H.W. Whitlock, Jr., G.L.
Smith // Tetrahedron Lett. – 1965. – Vol. 6. – P. 1389–1393.47. More, S. S. Synthesis of novel 5-alkyl/aryl/heteroaryl substituted diethyl 3,4-dihydro2H-pyrrole-4,4-dicarboxylates by aziridine ring expansion of 2-[(aziridin-1-yl)-1alkyl/aryl/heteroaryl-methylene]malonic acid diethyl esters / S. S. More, T. K.Mohan, Y. S. Kumar, U. K. S. Kumar, N. B. Patel // Beilstein J. Org. Chem. – 2011. –Vol. 7. – P. 831–838.14948.
Kumar, U. K. S. A New Route to Spiropyrrolidinyl-oxindole Alkaloids via Iodide IonInduced Rearrangement of [(N-Aziridinomethylthio)methylene]-2-oxindoles / U. K.S. Kumar, H. Ila, H. Junjappa // Org. Lett. – 2001. – Vol. 3. – P. 4193–4196.49. Heine, H. W. The Isomerization of Some 1-Aroylaziridines II / H. W. Heine, M. E.Fetter, E. M. Nicholson // J. Am. Chem. Soc. – 1959. – Vol. 81. – P. 2202–2204.50. Heine, H. W. Aziridines. XII.
The Isomerization of Some cis-and trans-1-pNitrobenzoyl-2, 3-Substituted Aziridines / H. W. Heine, D. C. King, L. A. Portland //J. Org. Chem. – 1966. – Vol. 31. – P. 2662–2665.51. Heine, H. W. Aziridines. XVI. Isomerization of some 1-aroylaziridines / H. W. Heine,M.
S. Kaplan // J. Org. Chem. – 1967. – Vol. 32. – P. 3069–3074.52. Foglia, T. A. Stereochemistry of the isomerization of N-acyl-2,3-disubstitutedaziridines to Δ2-oxazolines / T. A. Foglia, L. M. Gregory, G. Maerker // J. Org. Chem.– 1970. – Vol. 35. – P. 3779–3785.53. Heine, H. W. The isomerization and dimerization of aziridine derivatives. IV / H. W.Heine, W. G. Kenyon, E. M. Johnson // J. Am. Chem. Soc. – 1961. – Vol. 83. – P.2570–2574.54.
Heine, H. W. The Isomerization of Aziridine Derivatives / H. W. Heine // Angew.Chem. Int. Ed. – 1962. – Vol. 1. – P. 528–532.55. Eastwood, F. W. Preparation of new 2,4-disubstituted oxazoles from N-acylaziridines/ F. W. Eastwood, P. Perlmutter, Q. Yang // J. Chem. Soc., Perkin Trans. – 1997. –Vol. 1. – P. 35–42.56. Samimi, H.
A. An Efficient Synthesis of 5-Benzoyloxazolines by Regio- and Stereocontrolled Reaction of N-Substituted 2-Benzoylaziridines Under MicrowaveIrradiation / H. A. Samimi, M. Mamaghani, K. J. Tabatabaeian // Heterocycl. Chem. –2008. – Vol. 45. – P. 1765–1770.57. Samimi, H. A. Regio-controlled and Stereo-controlled Ring Expansion of NSubstituted-2-Benzoylaziridines Using Fe(NO3)3 / H. A.
Samimi, Z. Shams // J.Heterocycl. Chem. – 2014. – Vol. 51. – P. 1659–1663.58. Cardillo, G. Ring expansion of N-acyl aziridine-2-imides to oxazoline-4-imides,useful precursors of pure β-Hydroxy α-aminoacids / G. Cardillo, L. Gentilucci, A.Tolomelli, C. Tomasini // Tetrahedron Lett. – 1997. – Vol. 38. – P. 6953–6956.15059. Bonini, B. F. Synthesis of ferrocenyl-oxazolines by ring expansion of N-ferrocenoylaziridine-2-carboxylic esters / B. F. Bonini, M.
Fochi, M. Comes-Franchini, A. Ricci,L. Thijs, B. Zwanenburg // Tetrahedron: Asymmetry. – 2003. – Vol. 14. – P. 3321–3327.60. Martin, A. Phosphine-Catalyzed Heine Reaction / A. Martin, K. Casto, W. Morris, J.B. Morgan // Org. Lett. – 2011. – Vol. 13. – P. 5444–5447.61. Nishiguchi, T. Acid-catalyzed isomerization of 1-acyl- and 1-thioacylaziridines. I.Mechanism of nucleophilic substitution / T. Nishiguchi, H. Tochio, A.
Nabeya, Y.Iwakura // J. Am. Chem. Soc. – 1969. – Vol. 91. – P. 5835–5841.62. Nishiguchi, T. Acid-catalyzed isomerization of 1-acyl- and 1-thioacylaziridines. II.Orientation of ring opening / T. Nishiguchi, H. Tochio, A. Nabeya, Y. Iwakura // J.Am. Chem. Soc. – 1969. – Vol. 91. – P. 5841–5846.63. Heine, H. W.
The isomerization of some aziridine derivatives. III. A new synthesis of2-imidazolines / H. W. Heine, H. S. Bender // J. Org. Chem. – 1960. – Vol. 25. – P.461–463.64. Han, Y. Synthesis of Highly Substituted 2-Imidazolines through a Three-ComponentCoupling Reaction / Y. Han, Y.-X. Xie, L.-B. Zhao, M.-J. Fan, Y.-M.
Liang //Synthesis. – 2008. – P. 87–93.65. Jung, S.-H. Stereoselective synthesis of vicinal diamines from alkenes and cyanamide/ S.-H. Jung, H. Kohn // J. Am. Chem. Soc. – 1985. – Vol. 107. – P. 2931–2943.66. Claudi, F. Isomerization of 4-(1-aziridinyl)quinazolines to 2,3-dihydroimidazo [1,2c]quinazolines / F. Claudi, P. Franchetti, M.
Grifantini, S. Martelli // J. Org. Chem. –1974. – Vol. 39. – P. 3508–3511.67. DeWald, H. A. Synthesis and potential antipsychotic activity of 1H-imidazo[1,2c]pyrazolo[3,4-e]pyrimidines / H. A. DeWald, N. W. Beeson, F. M. Hershenson, L.D. Wise, D.
A. Downs, T. G. Heffner, L. L. Coughenour, T. A. Pugsley // J. Med.Chem. – 1988. – Vol. 31. – P. 454–461.68. Heine, H. W. The isomerization of aziridine derivatives. V. The formation of 1-arylΔ2-1,2,3-triazolines from 1-arylazoaziridines / H. W. Heine, D. A. Tomalia // J.Amer.
Chem. Soc. – 1962. – Vol. 84. – P. 993–995.69. Atkinson, R. S. A vinylaziridine to pyrroline rearrangement / R. S. Atkinson, C. W.Rees // Chem. Commun. (London). – 1967. – P. 1232–1232.15170. Mente, P. G. Aziridines. XXIV. Reactions of derivatives of 2-vinylaziridine / P. G.Mente, H. W. Heine // J. Org. Chem.
– 1971. – Vol. 36. – P. 3076–3078.71. Hudlicky, T. Microbial oxidation of chloroaromatics in the enantiodivergent synthesisof pyrrolizidine alkaloids: trihydroxyheliotridanes / T. Hudlicky, H. Luna, J. D. Price,F. Rulin // J. Org. Chem. – 1990. – Vol. 55. – P. 4683–4687.72. Borel, D. Isomerisation thermique de vinyl-2 aziridines N-substituees / D.
Borel, Y.Gelas-Mialhe, R. Vessière // Can. J. Chem. – 1976. – Vol. 54. – P. 1590–1598.73. Fugami, K. Pd(0) promoted transformation of N-tosyl-2-(1,3-butadienyl)-aziridineinto N-tosyl-2-vinyl-3-pyrroline / K. Fugami, Y. Morizawa, K. Oshima, H. Nozaki //Tetrahedron Lett. – 1985. – Vol. 26. – P. 857–860.74. Brichacek, M. Lewis Acid Catalyzed [1,3]-Sigmatropic Rearrangement of VinylAziridines / M. Brichacek, D.-E.
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