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Preliminary report of this work: N. Ono, H. Miyake, and A. Kaji, J. Chem. Soc., Chem. Commun., 1982, 33.
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Reviews of the Diels-Alder reaction using nitroalkenes
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Reviews of the Diels-Alder reaction using nitroalkenes: S. S. Novikov, G. A. Shvekhgeimer, and A. A. Dudinskaya, Russian Chem. Rev., 1960, 29, 79
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Houben-Weyl-Miiller, George Thieme Verlag, Stuttgart
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O. V. Schickh, G. Apel, H. G. Padeken, H. H. Schwartz, and A. Segnitz, in Houben-Weyl-Miiller: Methoden der Organischen Chemie, vol. 10/1, George Thieme Verlag, Stuttgart, 1971
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Seebach, D.1
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0000485677
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Recent examples of the Diels-Alder reaction of nitroalkenes: nitroethylene
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Recent examples of the Diels-Alder reaction of nitroalkenes: nitroethylene: D. Ranganathan, C. B. Rao, S. Ranganathan, A. K. Mehrotra, and R. Iyengar, J. Org. Chem., 1980, 45, 1185
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33845551929
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1-nitroprop-l-ene
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1-nitroprop-l-ene: P. A. Grieco, K. Yoshida, and P. Garner, J. Org. Chem., 1983, 48, 3137
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Grieco, P.A.1
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p-nitroacrylate
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p-nitroacrylate: P. A. Grieco, R. E. Zelle, R. Lis, and J. Finn, J. Am. Chem. Soc, 1983,105,1403
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33845379281
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intramolecular Diels-Alder reactions of nitroalkenes
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intramolecular Diels-Alder reactions of nitroalkenes: M. J. Kurth, M. J. O’Brien, H. Hope, and M. Yanock, J. Org. Chem., 1985, 50, 2626.
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H. B. Hass, A. G. Susie, and R. L. Heider, J. Org. Chem., 1950, 15, 8.
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Hass, H.B.1
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R. V. C. Carr, R. V. Williams, and L. A. Paquette, J. Org. Chem., 1983, 48,4976
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W. A. Kinney, G. D. Crouse, and L. A. Paquette, J. Org. Chem., 1983, 48, 4986.
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N. Ono, H. Miyake, R. Tamura, and A. Kaji, Tetrahedron Lett., 1981, 22, 1705
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N. Ono, A. Kamimura, H. Miyake, I. Hamamoto, and A. Kaji, J. Org. Chem., 1985, 50, 3692
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Ono, N.1
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19
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0001105970
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Rather drastic conditions are required for denitration of secondary nitro groups
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Rather drastic conditions are required for denitration of secondary nitro groups, N. Ono, H. Miyake, and A. Kaji, J. Org. Chem., 1984, 49, 4997.
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0001268077
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For example, the Diels-Alder reaction of ethylene with butadiene requires temperature of 175 °C and pressure 6 000 p.s.i
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For example, the Diels-Alder reaction of ethylene with butadiene requires temperature of 175 °C and pressure 6 000 p.s.i., P. D. Bartlett and K. E. Schueller, J. Am. Chem. Soc., 1968, 90, 6071.
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Bartlett, P.D.1
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0013164330
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Similar elimination of methanol to givex,β-unsaturated carbonyl compounds is often reported
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Similar elimination of methanol to give x,β-unsaturated carbonyl compounds is often reported, T. Shono, H. Nishiguchi, T. Komamura, and M. Sasaki, J. Am. Chem. Soc, 1979,101,984
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N. Ono, A. Kamimura, and A. Kaji, Tetrahedron Lett., 1986, 27, 1595.
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Tetrahedron Lett.
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A. A. Dudinskaya, G. A. Shvekhgeimer, and S. S. Novikov, Izv. Akad. SSSR., 1961, 182, 524
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