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Stigliani, W. M.; Laurie, V. W.; Li, J. C. J. Chem. Phys. 1975, 62, 1890. Kasai, P. H.; Myers, R. J.; Eggers, D. F. Jr.; Wiberg, K. B. J. Chem. Phys. 1959,30, 512. Dunitz, J. D.; Feldman, H. G.; Schomaker, V. J. Chem. Phys. 1952, 20, 1708.
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Kasai, P.H.1
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Stigliani, W. M.; Laurie, V. W.; Li, J. C. J. Chem. Phys. 1975, 62, 1890. Kasai, P. H.; Myers, R. J.; Eggers, D. F. Jr.; Wiberg, K. B. J. Chem. Phys. 1959,30, 512. Dunitz, J. D.; Feldman, H. G.; Schomaker, V. J. Chem. Phys. 1952, 20, 1708.
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Dunitz, J.D.1
Feldman, H.G.2
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(b) Review: Halton, B.; Banwell, M. G. In The Chemistry of the Cyclopropyl Group; Rappoport, Z., Ed., Wiley: New York, 1987; Chapter 21, 1223.
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Halton, B.1
Banwell, M.G.2
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9
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Houben-Weyl, Thieme: Stuttgart
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(d) Wendisch, D. In Houben-Weyl, Methoden der Organischen Chemie, 1971; Thieme: Stuttgart, Vol. 4/3, pp 679.
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(e) Gloss, G. L. In Advances in Alicyclic Chemistry; Hart, H., Karabatsos, G., Eds.; 1966; Vol. 1, p 53.
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(b) Dijachenko, A. I.; Agre, S. A.; Rudashevskaya, T. Y.; Shafran, R. M.; Nefedov, O. M. Izv. Akad. Nauk. SSSR, 1984, 2820; Engl. Transl. 1984, 33, 2585.
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Rudashevskaya, T.Y.3
Shafran, R.M.4
Nefedov, O.M.5
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84987110619
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(b) Dijachenko, A. I.; Agre, S. A.; Rudashevskaya, T. Y.; Shafran, R. M.; Nefedov, O. M. Izv. Akad. Nauk. SSSR, 1984, 2820; Engl. Transl. 1984, 33, 2585.
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15
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85033822536
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unpublished results
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Binger, P., unpublished results.
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Binger, P.1
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23
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84953492347
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Sodium bis(trimethylsilyl)amide was prepared according to the following references: (a) Wannagat, U.; Niederprüm, H. Chem. Ber. 1961, 94, 1540. (b) Krüger, C.; Rochow, E. G.; Wannagat, U. Chem. Ber. 1963, 96, 2132.
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Wannagat, U.1
Niederprüm, H.2
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24
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84857445436
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Sodium bis(trimethylsilyl)amide was prepared according to the following references: (a) Wannagat, U.; Niederprüm, H. Chem. Ber. 1961, 94, 1540. (b) Krüger, C.; Rochow, E. G.; Wannagat, U. Chem. Ber. 1963, 96, 2132.
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Krüger, C.1
Rochow, E.G.2
Wannagat, U.3
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3643052272
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Battiste, M. A.; Sprouse, C. T., Jr. Tetrahedron Lett. 1970, 4661; Tetrahedron Lett. 1969, 3165.
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33
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85033808497
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note
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The authors have deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystalographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK.
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36
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0001231628
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Cordes, M. H. J.; de Gala, S.; Berson, J. A. J. Am. Chem. Soc. 1994, 116, 11161.
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Cordes, M.H.J.1
De Gala, S.2
Berson, J.A.3
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37
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85033805349
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unpublished
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According to AM1 calculations, exo-adduct 3 is 3.1 kcal/mol more stable than endo-adduct 4. Rosenberg, M. G.; Brinker, U. H., unpublished.
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Rosenberg, M.G.1
Brinker, U.H.2
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