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Intra- and Intermolecular Hetero-Diels-Alder Reactions, Part 16. Part 15
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Intra- and Intermolecular Hetero-Diels-Alder Reactions, Part 16. Part 15: Tietze, L. F.; Brand, S.; Pfeiffer, T.; Antel, J.; Harms, K.; Sheldrick, G. M. J. Am. Chem. Soc. 1987,109, 921.
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Tietze, L.F.1
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Harms, K.5
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For newer reviews on the intramolecular Diels-Alder reaction, see: (a) (b) Oppolzer, W. Angew. Chem., Int. Ed. Engl. 1984, 23, 876. (c) Taber, D. F. Intramolecular Diels-Alder and Alder Ene Reactions; Springer Verlag: New York, 1984. (d) Fallis, A. G. Can. J. Chem. 1984,62,183. (e) Boger, D. L. Tetrahedron 1983, 39, 2869. (f) Weinreb, S. M.; Staib, R. R. Tetrahedron 1982, 38, 3087. (g) Brieger, G.; Bennett, J. N. Chem. Rev. 1980,80,63. (h) Sauer, J.; Sustmann. R. Angew. Chem., Int. Ed. Engl. 1980. 19. 779.
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For newer reviews on the intramolecular Diels-Alder reaction, see: (a) Ciganek, E. Org. React. (N. Y.) 1984,32,1. (b) Oppolzer, W. Angew. Chem., Int. Ed. Engl. 1984, 23, 876. (c) Taber, D. F. Intramolecular Diels-Alder and Alder Ene Reactions; Springer Verlag: New York, 1984. (d) Fallis, A. G. Can. J. Chem. 1984,62,183. (e) Boger, D. L. Tetrahedron 1983, 39, 2869. (f) Weinreb, S. M.; Staib, R. R. Tetrahedron 1982, 38, 3087. (g) Brieger, G.; Bennett, J. N. Chem. Rev. 1980,80,63. (h) Sauer, J.; Sustmann. R. Angew. Chem., Int. Ed. Engl. 1980. 19. 779.
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In SelectivityA Goal for Synthetic Efficiency
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Bartmann, W., Trost, B. M., Eds.; (4) The abbreviation ni-de and i-de are used for noninduced and induced diastereoselective reactions, respectively. The first term is employed for the formation of chirality elements in an achiral environment; the second term is used for the formation under the influence of a chiral environment. Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1985, 24, 1052.
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Tietze, L. F. In SelectivityA Goal for Synthetic Efficiency; Bartmann, W., Trost, B. M., Eds.; Verlag Chemie: Weinheim 1984; p 299. (4) The abbreviation ni-de and i-de are used for noninduced and induced diastereoselective reactions, respectively. The first term is employed for the formation of chirality elements in an achiral environment; the second term is used for the formation under the influence of a chiral environment. Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1985, 24, 1052.
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Tietze, L.F.1
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Tietze, L. F.; V. Kiedrowski, G.; Harms, K.; Clegg, W.; Sheldrick, G. Angew. Chem., Int. Ed. Engl. 1980, 19, 134.
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(b) Tietze, L. F.; Brumby, T., unpublished.
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Tietze, L. F.; Stegelmeier, H.; Harms, K.; Brumby, T. Angew. Chem., Int. Ed. Engl. 1982, 21, 863. (b) Tietze, L. F.; Brumby, T., unpublished.
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Tietze, L. F.; Brand, S.; Pfeiffer, T. Angew. Chem., Int. Ed. Engl. 1985, 24, 784.
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Brown, F. K.; Houk, K. N. Tetrahedron Lett. 1985, 26, 2297. Houk, K. N.; Lin, Y. T.; Brown, F. K. J. Am. Chem. Soc. 1986,108, 554.
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For an example, see: See also: Huisgen, R.; Mloston, G.; Langhals, E. J. Org. Chem. 1986, 51 4085.
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For an example, see: Tacconi, G.; Leoni, M.; Righetti, P.; Desi-moni, G.; Oberti, R.; Comin, F. J. Chem. Soc., Perkin Trans. 1 1979, 2687. See also: Huisgen, R.; Mloston, G.; Langhals, E. J. Org. Chem. 1986, 51 4085.
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For an example, see: Klarner, F. G. ; Dogan, B. M. J.; Ermer, O.; von Doering, W. E.; Cohen, M. P. Angew. Chem., Int. Ed. Engl. 1986,24,108.
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For an example, see: Martin, S. F.; Tu, C.; Chou, T. J. Am. Chem. Soc, 1980, 102, 5274. Klarner, F. G. ; Dogan, B. M. J.; Ermer, O.; von Doering, W. E.; Cohen, M. P. Angew. Chem., Int. Ed. Engl. 1986,24,108.
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Firestone, R. A. Tetrahedron 1977, 33, 3009. Firestone, R. A. Heterocycles 1987, 25,61.
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