Диссертация (1150389), страница 27
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Uemura, E. Wada // Tetrahedron Lett.–1992. – Vol. 33. – P. 78897892.139[14] Kanemasa, S. Metal Ion-Mediated Diastereoface-Selective Nitrone Cycloadditions.Reaction Mechanism for the Reversal of Regioselectivity Observed in the Magnesium and ZincIon-Mediated Nitrone Cycloadditions of Allylic Alcohols / S. Kanemasa, T.
Tsuruoka, H.Yamamoto // Tetrahedron Lett.–1995. – Vol. 36. – P. 5019-5022.[15] Tamura, O. One Step Bicyclization by Way of Tandem Transesterification, Intramolecular1,3-Dipolar Cycloaddition of α-Methoxycarbonylnitrones with Ally1 Alcohols in the Presence ofTitanium Isopropoxide / O. Tamura, T. Yamaguchi, K. Noe, M. Sakamoto // Tetrahedron Lett. –1993. – Vol. 34. – P. 4009-4010.[16] Tamura, O. Studies on Tandem Transesterification and Intramolecular Cycloaddition ofNitrones. 1. Sequential Bicyclization of α-Methoxycarbonylnitrones with Allyl Alcohols / O.Tamura, T. Okabe, T. Yamaguchi, K. Gotanda, K. Noe, M.
Sakamoto // Tetrahedron. – 1995. –Vol. 51. – P. 107-118.[17] Tamura, O. Studies on Tandem Transesterification and Intramolecular Cycloaddition ofNitrones. 1. Sequential Bicyclization of α,α-Dialkoxycarbonylnitrones with Allyl Alcohols / O.Tamura, T. Okabe, T. Yamaguchi, J. Kotani, K. Gotanda, M. Sakamoto // Tetrahedron. – 1995.
–Vol. 51. – P. 119-128.[18] Tamura, O. Tandem Transesterification and Intramolecular Cycloaddition of αMethoxycarbonylnitrones with Chiral Acyclic Allyl Alcohols: Systematic Studies on the FactorsAffecting Diastereofacial Selectivity of the Cycloaddition / O. Tamura, N. Mita, T. Okabe, T.Yamaguchi, C. Fukushima, M. Yamashita, Y. Morita, N. Morita, H. Ishibashi, M.
Sakamoto // J.Org. Chem.–2001. – Vol. 66. – P. 2602-2610.[19] Kanemasa, S. Magnesium Bromide-Promoted E/Z-Isomerization of Carbonyl-ConjugatedNitrones and Highly Stereo- and Regioselective Cycloadditions to Allylic AlcoholDipolarophiles / S.
Kanemasa, T. Tsuruoka // Chem. Lett. – 1995. – Vol. 24. – P. 49-50.[20] Inouye, Y. The Configurations of N-Methyl- and N-t-Butyl-α-methoxycarbonylmethanimineN-Oxides / Y. Inouye, K. Tanaka, H. Kakisawa // Bull. Chem. Soc. Jpn. – 1983. – Vol. 56. – P.3541-3542.[21] Inouye, Y. Novel E–Z Equilibrium Of N-Alkyl- α –Alkoxycarbonylnitrone In Solution / Y.Inouye, J. Hara, H. Kakisawa // Chem. Lett.
– 1980. – Vol. 9. – P. 1407-1410.[22] Aurich, H. G. Aromatic Solvent-Induced Shifts In The 1H-NMR Spectra Of Nitrones / H. G.Aurich, M. Franzke, H. P. Kesselheim // Tetrahedron. – 1992. – Vol. 48. – P. 663-668.[23] Tamura, O. Chelation Controlled 1,3-Dipolar Cycloaddition of 5,6-Dihydro-5-phenyl-l,4oxazin-2-one N-Oxide with Allyl Alcohols: A Short-step Synthesis of Clavalanine Intermediate /O. Tamura, T. Kuroki, Y. Sakai, J. Takizawa, J. Yoshino, Y.
Morita, N. Mita, K. Gotanda, M.Sakamoto // Tetrahedron Lett. – 1999. – Vol. 40. – P. 895-898.140[24] Jones, A. D. On the Lewis acid-induced [1,3]-dipolar cycloaddition of allylic andhomoallylic alcohols to N-methyl-C-phenyl nitrone / A. D. Jones, D. W. Knight, S.
R. Thornton// J. Chem. Soc., Perkin Trans. 1 – 1999. – P. 3337-3344.[25] Shimizu, T. The Effects of Lewis Acid on the 1,3-Dipolar Cycloaddition Reaction of CArylaldonitrones with Alkenes / T. Shimizu, M. Ishzaki, N. Nitada // Chem. Pharm. Bull. –2002. – Vol. 50. – P. 908-921.[26] Bortolini, O. 1,3-Cycloaddition of nitrones in ionic liquids catalyzed byEr(III): an easyaccess to isoxazolidines / O.
Bortolini, A. De Nino, L. Maiuolo, B. Russo, G. Sindona, A. Tocci// Tetrahedron Lett.–2007. – Vol. 48. – P. 7125-7128.[27] Ellis, W. W. Homogeneous Catalysis. Metallocene Catalysts for [3+2] Nitrone-OlefinCycloaddition Reactions / W. W. Ellis, A. Gavrilova, L. Liable-Sands, A. L. Rheingold, B.Bosnich // Organometallics. – 1999. – Vol. 34. – P. 332-338.[28] Stanley, L.
M. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions / L. M.Stanley, M. P. Sibi // Chem. Rev. – 2008. – Vol. 108. – P. 2887-2902.[29] Hashimoto, T. Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions / T.Hashimoto, K. Maruoka // Chem. Rev. – 2015. – Vol.
115. – P. 5366-5412.[30] Berthet, M. Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry / M.Berthet, T. Cheviet, G. Dujardin, I. Parrot, J. Martinez // Chem. Rev. – 2016. – Vol. 116. – P.15235–15283.[31] Pellissier, H. Asymmetric 1,3-dipolar cycloadditions / H. Pellissier // Tetrahedron. – 2007. –Vol. 63. – P. 3235-3285.[32] Bădoiu, A. Asymmetric Lewis Acid-Catalyzed 1,3-Dipolar Cycloadditions / A. Bădoiu, Y.Brinkmann, F.
Viton, E. P. Kűndig // Pure Appl. Chem. – 2008. – Vol. 80. – P. 1013-1018.[33] Kissane, M. Asymmetric 1,3-Dipolar Cycloadditions of Acrylamides / M. Kissane, A. R.Maguire // Chem. Soc. Rev. – 2012. – Vol. 256. – P. 938-952.[34] Xing, Y. Organocatalytic and metal-mediated asymmetric [3+2] cycloaddition reactions / Y.Xing, N.-X. Wang // Coord. Chem. Rev. – 2010. – Vol. 39. – P. 845-883.[35] Seerden, J.-P. G. Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with Ketene AcetalsCatalyzed by Chiral Oxazaborolidines / J.-P. G.
Seerden, A. W. A. Schotte op Reimer, H. W.Scheeren // Tetrahedron Lett.–1994. – Vol. 35. – P. 4419-4422.[36] Gothelf K. V. Transition-Metal Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactionsbetween Alkenes and Nitrones / K. V. Gothelf, K. A. Jørgensen // J. Org. Chem. – 1994. – Vol.59. – P. 5687-5691.[37] Murahashi, S.-I. Asymmetric 1,3-Dipolar Cycloaddition of Cyclic Nitrones to CrotonicAcid Derivatives Bearing Chiral Auxiliaries. Synthesis of Optically Active β-Amino Acids, (+)141Sedridine, and (+)-Hygroline / S.-I.
Murahashi, Y. Imada, M. Kohno, T. Kawakami // Synlett.–1993. –P. 7125-7128.[38] Huang, Z.-Z. Diastereoselectivity-Switchable and Highly Enantioselective 1,3-DipolarCycloaddition of Nitrones to Alkylidene Malonates / Z.-Z. Huang, Y.-B. Kang, J. Zhou, M.-C.Ye, Y. Tang // Org. Lett.
– 2004. – Vol. 6. – 1677-1679.[39] Gothelf, K. V. Molecular Sieve Dependent Absolute Stereoselectivity in AsymmetricCatalytic 1,3-Dipolar Cycloaddition Reactions / K. V. Gothelf, R. G. Hazell, K. A. Jørgensen //J. Org. Chem. – 1998. – Vol. 63. – P. 5483-5488.[40] Sanchez-Blanco, A. I. Lanthanide-Catalyzed Endo- and Enantioselective 1,3-DipolarCycloaddition Reactions of Nitrones with Alkenes / A. I. Sanchez-Blanco, K. V. Gothelf, K.
A.Jørgensen // Tetrahedron Lett.–1994. – Vol. 38. – P. 7923-7926.[41] Barroso, S. Highly Enantioselective Nitrone Cycloadditions with 2-Alkenoyl Pyridine NOxides Catalyzed by Cu(II)-BOX Complexes / S. Barroso, G. Blay, M. C. Muñoz, J. R. Pedro //Org. Lett. – 2011. – Vol. 13. – P. 402-405.[42] Sibi, M. P. Copper(II)-Catalyzed Exo and Enantioselective Cycloadditions of AzomethineImines / M.
P. Sibi, D. Rane, L. M. Stanley, T. Soeta // Org. Lett. – 2008. – Vol. 10. – P. 29712974.[43] Sibi, M. P. Exo Selective Enantioselective Nitrone Cycloadditions / M. P. Sibi, Z. Ma, C. P.Jasperse // J. Am. Chem. Soc. – 2004. – Vol. 126. – P. 718-719.[44] Hashimoto, T. Catalytic Enantioselective 1,3-Dipolar Cycloaddition of C,N-CyclicAzomethine Imines with α,β-Unsaturated Aldehydes / T. Hashimoto, Y.
Maeda, M. Omote, H.Nakatsu, K. Maruoka // J. Am. Chem. Soc. – 2010. – Vol. 132. – P. 4076-4077.[45] Anderson, L. Diverse Applications of Nitrones for the Synthesis of HeterocyclicCompounds / L. Anderson, // Asian J. Org. Chem. – 2016. – Vol.
5. – P. 9-30.[46] Xu, X. The [3 + 3]-Cycloaddition Alternative for Heterocycle Syntheses: CatalyticallyGenerated Metalloenolcarbenes as Dipolar Adducts / X. Xu, M. P. Doyle // Acc. Chem. Res. –2014. – Vol. 47. – P. 1396-1405.[47] Cardona, F. The Discovery of Novel Metal-Induced Reactions of Nitrones: Not OnlyElectrophiles and Reagents for [3+2] Cycloadditions / F. Cardona, A. Goti // Angew. Chem. Int.Ed. – 2005.
– Vol. 44. – P. 7832-7835.[48] Qian, D. Gold-Catalyzed Cascade Reactions for Synthesis of Carbo- and Heterocycles:Selectivity and Diversity / D. Qian, J. Zhang // Chem. Rec. – 2014. – Vol. 14. – P. 280-302.[49] Shintani, R. Palladium-Catalyzed [3 + 3] Cycloaddition of Trimethylenemethane withAzomethine Imines / R. Shintani, T. Hayashi // J. Am. Chem.
Soc. – 2006. – Vol. 128. – P.6330-6331.142[50]Shintani,R.Palladium-CatalyzedAsymmetric[3+3]CycloadditionofTrimethylenemethane Derivatives with Nitrones / R. Shintani, S. Park, W.-L. Duan, T. Hayashi,// Angew. Chem. Int. Ed. – 2007. – Vol. 46. – P. 5901-5903.[51] Na, R. Phosphine-Catalyzed Annulations of Azomethine Imines: Allene-Dependent [3 + 2],[3 + 3], [4 + 3], and [3 + 2 + 3] Pathways / R. Na, C. Jing, Q.