Диссертация (1150039), страница 21
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R. Ruthenium Catalyzed Synthesis of Enaminones // Org. Lett. – 2012. –Vol. 14. – P. 440-443.[83] Regitz, M.; Liedhegener, A. Reactionen aktiver Melhylenverbindungen mit Aziden.XII. Synthese von Diacyldiazomethanen durch Diazogruppenubertagung // Chem. Ber. –1966. – Vol. 99. – P. 3128-3147.[84] Коробицына, И. К.; Николаев, В. А. Химия диазокарбонильных соединений.
I.Получение, ИК и УФ спектры некоторых 2-диазо-1,3-дикетонов // ЖОрХ. – 1976. –Т. 12. – С. 1244-1251.132[85]Николаев,В.диазодикарбонильныхА.;Попик,В.соединений.В.;IX.Коробицына,И.К.КонформационныйХимияанализпространственно-затрудненных 2-диазо-1,3-дикетонов // ЖОрХ. – 1991. – Т. 27.
–С. 505-521.[86] Tjoeng, F. S.; Heavner, G. A. Synthesis of a New Photolabile Support. 4-(2Chloropropionyl)phenylacetamidomethyl-resin and its Application in Solid-phasePeptide Synthesis // J. Org. Chem. – 1983. – Vol. 48. – P. 355-359.[87] Danheiser, R.L.; Miller, R.F.; Brisbois, R.G.; Park, S.Z. An Improved Method forthe Synthesis of α-Diazo Ketones // J. Org.
Chem. – 1990. – Vol. 55. – P. 1959-1964.[88] Danheiser, R.L.; Brisbois, R.G.; Kowalczyk, J.J.; Miller, R.F. An AnnulationMethod for the Synthesis of Highly Substituted Polycyclic Aromatic and HeteroaromaticCompounds // J. Am. Chem. Soc. – 1990. – Vol. 112. – P. 3093-3100.[89] Sickert, M.; Schneider, C.
The Enantioselective, Bronsted Acid Catalyzed,Vinylogous Mannich Reaction // Angew. Chem. Int. Ed. – 2008. – Vol. 47. – P. 36313634.[90] Sickert, M.; Abels, F.; Lang, M.; Sieler, J.; Birkemeyer, C.; Schneider, C. TheBronsted Acid Catalyzed, Enantioselective Vinylogous Mannich Reaction // Chem. Eur.J. – 2010. – Vol. 16. – P. 2806-2818.[91] Abels, F.; Schneider, C. A Modified and Highly Useful Protocol for Bronsted AcidCatalyzed, Enantioselective, Vinylogous Mannich Reaction with Aliphatic Aldimines //Synthesis.
– 2011. – P. 4050-4058.[92] Giera, D. S.; Sickert, M.; Scneider, C. Bronsted Acid-Catalyzed, Enantioselective,Vinylogous Mannich Reaction of Vinylketene Silyl N,O-Acetals // Org. Lett. – 2008. –Vol. 10. – P. 4259-4262.[93] McRobb, F. M.; Crosby, I. T.; Yuriev, E.; Lane, J. R.; Capuano, B. HomobivalentLigandsofthePtypicalAntipsychoticClozapine:Design,Synthesis,andPharmacological Evaluation // J. Med.
Chem. – 2012. – Vol. 55. – 1622-1634.[94] Taylor, E. C.; McKillop, A. Facile Reductive Cyclizations. New Routes toHeterocycles. I // J. Am. Chem. Soc. – 1965. – Vol. 87. – P. 1984-1990.133[95] Wan, W.; Hou, J.; Jiang, H.; Yuan, Z.; Ma, G.; Zhao, G.; Hao, J. ReductiveAmination/Cyclization ofω-Trifluoromethyl Keto Esters to Trifluoromethylated δ-Amino Alcohols and Lactams // Eur. J. Org. Chem. – 2010. – P. 1778-1786.[96] Johnson, S. A.; Hunt, H. R.; Neuman, H.
M. Preparation and Properties ofAnhydrous Rhodium(II) Acetate and Some Adducts Thereof // J. Neorg. Chem. – 1963. –Vol. 2. – 960-962.[97] Cotton, F. A.; Murillo, C. A.; Walton, R. A. Multiple Bonds Between Metal Atoms// Springer-Verlag, N.-Y., 2005.[98] Qu, Z.; Shi, W.; Wang, J. A kinetic Study on the Pairwise Competition Reaction ofα-Diazo Esters with Rhodium(II) Catalysts: Implication for the Mechanism of Rh(II)Carbene Transfer // J. Org.
Chem. – 2001. – Vol. 66. – P. 8139-8144.[99] Lu, C.-D.; Liu, H.; Chen, Z.-Y.; Hu, W.-H.; Mi, A.-Q. The Rhodium CatalyzedThree-Component Reaction of Diazoacetates Titanium (IV) Alkoxides and Aldehydes //Chem. Commun. – 2005. – P. 2624-2626.[100] Ace, K. W.; Hussain, N.; Lathbury, D. C.; Morgan, D. O. Synthesis of an α(Aminooxy)arylacetic Ester by the Reaction of an α-Diazo Ester with nHydroxyphthalimide // Tetrahedron Lett. – 1995. – Vol. 36. – P. 8141-8144.[101] Nakamura, E.; Yoshikai, N.; Yamanaka, M. Mechanism of C-H BondActivation/C-C Bond Formation Reaction between Diazo Compound and AlkaneCatalyzed by Dirhodium Tetracarboxylate // J.
Am. Chem. Soc. – 2002. – Vol. 124. – P.7181-7192.[102] Liang, Y.; Zhou, H.; Yu, Z.-X. Why Is Cooper(I) Complex More Component ThanDirhodium(II) Complex in Catalytic Asymmetric O-H Insertion Reactions? AComputational Study of the Metal Carbenoid O-H Insertion into Water // J. Am. Chem.Soc. – 2009. – Vol. 131. – P.
17783-17785.[103] Clark, J. S.; Hansen, K. E. Intramolecular Reactions of Metal Carbenoids withAllylic Ethers: Is a Free Ylide Invoved in Every Case? // Chem. Eur. J. – 2014. – Vol. 20.– P. 5454-5459.134[104] Evans, P. A. Modern Rhodium-Catalyzed Organic Reactions // Wiley-VCH,Weinheim, 2005.[105] Xu, F.; Armstrong, D. J.; Zhou, G. X.; Simmons, B.; Hughes, D.; Ge, Z.;Grabowski, E. J. J. Mechanistic Evidence for an α-Oxoketene Pathway in the Formationof β-Ketoamides/Esters via Meldrum's Acid Adducts // J. Am.
Chem. Soc. – 2004. –Vol. 126. – P. 13002-13009.[106] George, L.; Wong, M. W.; Wentrup, C. Carboxyketenes, Methyleneketenes,Vinylketenes, Oxetandiones, Ynols, and Ylidic Ketenes from Meldrum's AcidDerivatives // Org. Biomol. Chem. – 2007. – Vol. 5. – P.
1437-1441.[107] Emtenas, H.; Soto, G.; Hultgren, S. J.; Marshall, G. R.; Almqvist, F.Stereoselective Synthesis of Optically Active β-Lactams, Potential Inhibitors of PilusAssembly in Pathogenic Bacteria // Org. Lett. – 2000. – Vol. 2. – P. 2065-2067.[108] Tidwell, T. T. The First Century of Ketenes (1905-2005): The Birth of a VersatileFamily of Reactive Intermediates // Angew. Chem. Int. Ed. – 2005. – Vol. 44. – P.
57785785.[109] Allen, A. D.; Tidwell, T. T. Ketenes and Other Cumulenes as ReactiveIntermediates // Chem. Rev. – 2013. – Vol. 113. – P. 7287-7342.[110] Song, R.-J.; Liu, Y.; Hu, R.-X.; Liu, Y.-Y.; Wu, J.-C.; Yang, X.-H.; Li, J.-H.Oxidative Cleavage of the Carbon-Carbon σ-Bond Using Reusable Copper on Iron //Adv.
Synth. Catal. – 2011. – Vol. 353. – P. 1467-1473.[111] Murata, S.; Suzuki, K.; Miura, M.; Nomura, M. Iron-catalyzed Oxidation of N,N(Dialkyl)acylmethylamines with Molecular Oxygen in the Presence of either 2Mercaptoethanol or Sodium Sulphide // J. Chem. Soc. Perkin. Trans. 1. – 1990. – P. 361365.[112] Tangari, N.; Tortorella, V. Regiospecific Oxidation of Cyclic Amino-compoundswith Ruthenium Tetroxide // J. Chem. Soc., Chem.
Commun. – 1975. – P. 71b-72.[113] Zhao, Y.; Ang, J. Q. L.; Nq, A. W. T.; Yeung, Y.-Y. Oxidative Transformation ofCyclic Ethers/Amines to Lactones/Lactams Using DIB/TBHP Protocol // RSC Adv. –2013. – Vol. 3. – P. 19765-19768.135[114] Doyle, M. P. Perspective on Dirhodium Carboxamidates as Catalysts // J. Org.Chem. – 2006. – Vol. 71. – P. 9253-9260.[115] Ratnikov, M. O.; Doyle, M.
P. Dirhodium Caprolactamate and tert-ButylHydroperoxide - a Universal System for Selective Oxidation // Mendeleev Commun. –2014. – Vol. 24. – P. 187-196.[116] Catino, A. J.; Forslund, R. E., Doyle, M. P. Dirhodium(II) Caprolactamate: AnExceptional Catalyst for Allylic Oxidation // J. Am. Chem. Soc. – 2004. – Vol. 126. – P.13622-13623.[117] Kirmse, W. 100 Years of the Wolff Rearrangement // Eur. J. Org. Chem. – 2002. –P. 2193-2256.[118] Bien, S.; Segal, Y. Catalyst-product Dependency in the Transition Metal CatalyzedDecomposition of Ethyl 3-Diazo-2-oxopropionate.
An Unusual Wolff Rearrangement //J. Org. Chem. – 1977. – Vol. 42. – P. 1685-1688.[119] Nakato, H.; Toshikazu, I. The Rhodium(II) Acetate-catalyzed Reaction ofDiacyldiazomethanes with Isothiocyanates: Formation of 2-Thioxo-2H-1,3-oxazin4(3H)-one // Bull. Chem. Soc. Japan. – 1993. – Vol. 66. – P. 238-244.[120] Yanez, E. C.; Almanza, R. C. Rhodium (II) Catalyzed Wolff Rearrangement of aCarbenoid Derived from an Indolyl Diazopropanedione // Rev. Soc.
Quim. Mex. – 2004.– Vol. 48. – P. 46-48.[121] Davies, J. D.; Kane, P. D.; Moody, C. J.; Slawin, A. M. Z. Control of CompetingN-H Insertion and Wolff Rearrangement in Dirhodium(II)-Catalyzed Reactions of 3Indolyl Diazoketoesters, Synthesis of a Potential Precursor to the Marine 5-(3Indolyl)oxazole Martefragin A // J. Org. Chem. – 2005. – Vol. 70. – P. 5840-5851.[122] Ceccherelli, P.; Curini, M.; Marcotullio, M. C.; Pisani, E.; Rosati, O.; Wenkert, E.UnusualProductsfromDirhodiumTetraacylate-catalyzedDecompositionofDiazoacetylcycloalkanes // Tetrahedron. – 1997.
– Vol. 53. – P. 8501-8506.[123] Ronan, B.; Bacque, E.; Barriere, J.-C. 17-Diazo Pristinamycin IIB Preparation andSynthetic Applications // Tetrahedron. – 2004. – Vol. 60. – P. 3819-3824.136[124] Marsden, S. P.; Pang, W.-K. Efficient, General Synthesis of Silylketenes via anUnusual Rhodium Mediated Wolff Rearrangement // Chem. Commun. – 1999. – P. 11991200.[125] Lawlor, M. D.; Lee, T. W.; Danheiser, R. L. Rhodium-catalyzed Rearrangement ofAlpha-diazo Thiol Esters to Thio-substituted Ketenes. Application in the Synthesis ofCyclobutanones, Cyclobutenones, and Beta-lactams // J. Org. Chem.
– 2000. – Vol. 65. –P. 4375-4384.[126] Boddaert, T.; Coquerel, Y.; Rodriguez, J. N-Heterocyclic Carbene-CatalyzedMichael Additions of 1,3-Dicarbonyl Compounds // Chem. Eur. J. – 2011. – Vol. 17. – P.2266-2271.[127] Carling, R. W.; Leeson, P. D.; Moore, K. W.; Smith, J. D.; Moyes, C.
R.; Mawer, I.M.; Thomas, S.; Chan, R.; Baker, R.; Foster, A. C.; Crimwood, S.; Kemp, J. A.;Marshall, G. R.; Tricklebank, M. D.; Saywell, K. L. 3-Nitro-3,4-dihydro-2(1H)quinolones. Excitatory Amino Acid Antagonists Acting at Glycine-Site NMDA and (RS)α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors // J.
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