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Berlin, B. Giese, Angew. Chem., 1983, Angew. Chem., Int. Ed. Engl., 1983, 753; D. J. Hart, Science, 1984, 223, 883; B. Giese, Angew. Chem., 1985, 97, 555; Angew. Chem., Int. Ed. Engl., 1985, 24, 553
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D. I. Davies and M. J. Parrott, ‘Free Radicals in Organic Synthesis,’ Springer Verlag, Berlin, 1978; B. Giese, Angew. Chem., 1983, 95, 771; Angew. Chem., Int. Ed. Engl., 1983, 22, 753; D. J. Hart, Science, 1984, 223, 883; B. Giese, Angew. Chem., 1985, 97, 555; Angew. Chem., Int. Ed. Engl., 1985, 24, 553.
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D. H. R. Barton and W. B. Motherwell, Pure Appl. Chem., 1981, 53, 15; H. H. Henning, F. Pragst, and J. Fuhrmann, Z. Chem., 1984, 24, 1; G. Stork in ‘Selectivity-A Goal for Synthetic Efficiency,’ eds. W. Bartmann and B. M. Trost, Verlag Chemie, Weinheim 1984, p. 281.
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B. Giese and J. Dupuis, Angew. Chem., 1983,95, 633; Angew. Chem., Int. Ed. Engl., 1983, 22, 622; B. Giese and K. Groninger, Tetrahedron Lett., 1984, 25, 2743; J. Dupuis, B. Giese, J. Hartung, M. Leising, H. G. Korth, and R. Sustmann, J. Am. Chem. Soc., 1985, 107, 4332.
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For leading references see, Specialist Periodical Report, London, 1983, p. 225; C. von Sonntag, Adv. Carbohydr. Chem. Biochem., 1980, 37, 7
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For leading references see: ‘Electron Spin Resonance,’ Specialist Periodical Report, The Royal Society of Chemistry, London, 1985, vol. 9, p. 151; 1983, vol. 8, p. 225; C. von Sonntag, Adv. Carbohydr. Chem. Biochem., 1980, 37, 7.
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R. O. C. Norman and R. J. Pritchett, J. Chem. Soc. B, 1967, 1329; P. R. West, G. Schnarr, and L. Sitwell, Tetrahedron Lett., 1977, 3869.
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B. C. Gilbert, D. M. King, and C. B. Thomas, J. Chem. Soc., Perkin Trans. 2, 1980, 1821; 1982, 169; Carbohydr. Res., 1984, 125, 217.
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Gilbert, B.C.1
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1981, 1186; in these papers, values of ca. 1.2 and 3.0 mT were reported for the coupling constants of equatorial and axial hydrogen atoms, respectively, in six-membered carbohydrate radicals
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B. C. Gilbert, D. M. King, and C. B. Thomas, J. Chem. Soc., Perkin Trans. 2, 1981, 1186; 1983, 675; in these papers, values of ca. 1.2 and 3.0 mT were reported for the coupling constants of equatorial and axial hydrogen atoms, respectively, in six-membered carbohydrate radicals.
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J. Chem. Soc., Perkin Trans. 2
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Gilbert, B.C.1
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H. Fischer and K. H. Hellwege, Springer Verlag, Berlin
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‘Landolt-Börnstein, New Series,’ vol. II/9b, eds. H. Fischer and K. H. Hellwege, Springer Verlag, Berlin, 1977.
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see also P. Deslongchamps, ‘Stereoelectronic Effects in Organic Chemistry,’ Pergamon Press, Oxford, 1983, pp. 29, 211
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R. U. Lemieux, K. B. Hendricks, R. V. Stick, and K. James, J. Am. Chem. Soc., 1975, 97, 4056; see also P. Deslongchamps, ‘Stereoelectronic Effects in Organic Chemistry,’ Pergamon Press, Oxford, 1983, pp. 29, 211.
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Lemieux, R.U.1
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1942 B. C. Gilbert, J. P. Larkin, and R. O. C. Norman, p. 794; B. C. Gilbert, M. Trenwith, and A. J. Dobbs, ibid., 1772
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A. J. Dobbs, B. C. Gilbert, and R. O. C. Norman, J. Chem. Soc., Perkin Trans. 2, 1972, 786; B. C. Gilbert, J. P. Larkin, and R. O. C. Norman., p. 794; B. C. Gilbert, M. Trenwith, and A. J. Dobbs., 1974, 1772.
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A. J. L. Beckwith and J. C. Easton, p. 615
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V. Malatesta and K. U. Ingold, J. Am. Chem. Soc., 1981, 103, 609; A. J. L. Beckwith and J. C. Easton, p. 615.
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The Anomeric Effect and Related Stereoelectronic Effects at Oxygen
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Berlin
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A. J. Kirby, ‘The Anomeric Effect and Related Stereoelectronic Effects at Oxygen,’ Springer Verlag, Berlin, 1983, p. 128.
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For reviews see, P. D. Sullivan and E. M. Menger, Adv. Magn. Reson., 1977, 1
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For reviews see J. K. Kochi, Adv. Free-Radical Chem., 1975, 5, 189; P. D. Sullivan and E. M. Menger, Adv. Magn. Reson., 1977, 9, 1.
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H. Fischer and K. H. Hellwege, Springer Verlag, Berlin
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‘Landolt-Börnstein, New Series,’ vol. II/9b, eds. H. Fischer and K. H. Hellwege, Springer Verlag, Berlin, 1977., pp. 271-289f
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0039316973
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In a recent low-temperature ESR/ENDOR study, a slight out-ofplane bent angle of ca. 2.3 ± 1° was determined in a prototypal ‘CH2OR radical
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W. A. Bernhard, T. L. Horning, and K. R. Mercer
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In a recent low-temperature ESR/ENDOR study, a slight out-ofplane bent angle of ca. 2.3 ± 1° was determined in a prototypal ‘CH2OR radical; W. A. Bernhard, T. L. Horning, and K. R. Mercer, J. Phys. Chem., 1984, 88, 1317.
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