3198
Helvetica Chimica Acta – Vol. 88 (2005)
[16] a) D. J. Mc Caldin, Chem. Rev. 1960, 60, 39 (auf S. 47); b) H. Ardill, M. J. R. Dorrity, R. Grigg, J. F. Malone,
M.-S. Leon-Ling, V. Sridharan, S. Thianpatanagul, Tetrahedron 1990, 46, 6433; c) H. Ardill, X. L. R. Fon-
taine, R. Grigg, D. Henderson, J. Montgomery, V. Sridharan, S. Surendrakumar, Tetrahedron 1990, 46,
6449; d) R. Grigg, H. Q. N. Gunaratne, J. Kemp, Tetrahedron 1990, 46, 6467.
[17] D. Pauley, F. Anderson, T. Hudlicky, Org. Synth., Coll. Vol. VIII 1993, 208; P. D. Magnus, M. S. Nobbs,
Synth. Commun. 1980, 10, 273.
[18] a) K. Schank, F. Werner, Liebigs Ann. Chem. 1979, 1977; b) K. Schank, F. Werner, Liebigs Ann. Chem.
1983, 1739; c) K. Schank, C. Schuhknecht, Chem. Ber. 1982, 115, 2000; d) K. Schank, C. Schuhknecht, Sul-
fur Lett. 1990, 12, 83 und 91; e) K. Schank, S. Moschel, Phosphorus, Sulfur, Silicon, Relat. Elem. 1993, 74,
419; f) K. Schank, M. Buschlinger, J. Prakt. Chem. 1995, 337, 196; g) K. Schank, S. Pistorius, M. Weiter, F.
Werner, J. Prakt. Chem. 1995, 337, 409; h) K. Schank, P. Beljan, J. Prakt. Chem. 1995, 337, 558; i) K. Schank,
H. Beck, M. Buschlinger, J. Eder, T. Heisel, S. Pistorius, C. Wagner, Helv. Chim. Acta 2000, 83, 801; j) K.
Schank, C. Marson, T. Heisel, K. Martens, C. Wagner, Helv. Chim. Acta 2000, 83, 3312; k) R. F. Langler, R.
K. Raheja, K. Schank, H. Beck, Helv. Chim. Acta 2001, 84, 1943; l) K. Schank, M. Weiter, R. Keasalar,
Helv. Chim. Acta 2002, 85, 2105; m) K. Schank, in ‘Recent Research Developments in Heterocyclic Che-
mistry’, Transworld Research Network, Kerala, 2003, Bd. I, S. 1–38; n) K. Schank, Helv. Chim. Acta 2004,
87, 2074; o) K. Schank, H. Beck, S. Pistorius, Helv. Chim. Acta 2004, 87, 2025.
[19] P. S. Bailey, in ‘Ozonation in Organic Chemistry’, Bd. II: ‘Nonolefinic Compounds’, Academic Press, 1982,
S. 175, 200.
[20] a) D. Bahnemann, E. S. Hart, J. Phys. Chem. 1982, 86, 252; b) L. E. Bennett, P. Warlop, Inorg. Chem. 1990,
29, 1975; c) L. Forni, D. Bahnemann, E. J. Hart, J. Phys. Chem. 1982, 86, 255; d) A. R. Forrester, V. Purus-
hotham, J. Chem. Soc., Faraday Trans. 1 1987, 83, 211.
[21] a) D. H. Giamalva, D. F. Church, W. A. Pryor, J. Am. Chem. Soc. 1986, 108, 6646; b) R. D. McAlpine, M.
Cocivera, H. Chen, Can. J. Chem. 1973, 51, 1682; c) P. S. Bailey, F. E. Potts, J. W. Ward, J. Am. Chem. Soc.
1970, 92, 230; d) A. A. Frimer, V. Marks, P. Gilinsky-Sharon, G. Aljadeff, H. E. Gottlieb, J. Org. Chem.
1995, 60, 4510.
[22] M. L. Chanon, M. L. Tobe, Angew. Chem. 1982, 94, 27 (Angew. Chem., Int. Ed. 1982, 21, 1).
[23] K. Schank, in ‘Methodicum Chimicum’, Hrsg. F. Korte, Thieme, Stuttgart, 1974, Academic Press, New
York, San Francisco, London, 1974, Bd. 6, Kap. 7, S. 165–209 (dort S. 191).
[24] Y. L. Chow, in ‘Reactive Intermediates 1’, Hrsg. R. A. Abramovitch, Plenum Press, New York, 1980, S. 151;
G. Pandey, Synlett 1992, 576; D. A. Armstrong, A. Rauk, D. Yu, J. Am. Chem. Soc. 1993, 115, 666.
[25] S. Hünig, H. Hoch, Fortschr. Chem. Forsch., Top. Curr. Chem. 1970, 14(3), 257, 265.
[26] J. Smuszkowicz, E. Cerda, M. F. Grostic, J. F. Zieserl, Tetrahedron Lett. 1967, 8, 3969.
[27] a) T.-L. Ho, in ‘Heterocyclic Fragmentation of Organic Molecules’, Wiley-Interscience, 1993, S. 159 ff.; b)
L. I. Smith, E. R. Rogier, J. Am. Chem. Soc. 1951, 73, 3837; d) J. Meinwald, O. L. Chapman, J. Am. Chem.
Soc. 1959, 81, 5800; c) J. F. Biellmann, M. P. Goeldner, Tetrahedron 1971, 27, 1789; e) D. O. Spry, A. R.
Bhala, W. A. Spitzner, N. D. Jones, J. K. Swartzendruber, Tetrahedron Lett. 1984, 25, 2531; f) J. W. Streef,
H. C. van der Plas, Y. Y. Wie, J. P. Declercq, M. Van Meersche, Heterocycles 1987, 26, 585.
[28] a) A. S. Kende, Org. Reactions 1960, 11, 261; b) J. M. Conia, K. J. Robson, Angew. Chem. 1975, 87, 505
(Angew. Chem., Int. Ed. 1975, 14, 473).
[29] R. M. Moriarty, I. Prakasch, H. A. Mussallam, Tetrahedron Lett. 1984, 25, 5867.
[30] D. M. Lemal, K. I. Kawano, J. Am. Chem. Soc. 1962, 84, 1761; F. Roeterdink, J. W. Scheeren, W. H. Laar-
hoven, Tetrahedron Lett. 1983, 24, 2307; Z. Shi, R. P. Thummel, J. Org. Chem. 1995, 60, 5935.
[31] M. Traube, Ber. Dtsch. Chem. Ges. 1885, 18, 1887; M. Traube, Ber. Dtsch. Chem. Ges. 1893, 26, 1471; R.
Akaba, H. Sakuragi, K. Tokumaru, Tetrahedron Lett. 1984, 25, 665; S. Fukuzumi, N. Nishizawa, T. Tanaka,
J. Org. Chem. 1984, 49, 3571; T. Kiyota, M. Yamaji, H. Shizuka, J. Phys. Chem. 1996, 100, 672.
[32] C. A. Heller, in ‘Oxidation of Organic Compounds I’, Hrsg. F. R. Mayo, Am. Chem. Soc., Washington DC,
1968, Bd. 75, S. 225.
[33] a) S. Fallab, Angew. Chem. 1967, 79, 50 (Angew. Chem., Int. Ed. 1967, 6, 496); b) A. G. Lappin in ‘Redox
Mechanism in Inorganic Chemistry’, Ellis Horwood, New York, London, Toronto, Sydney, Tokyo, Singa-
pore, 1994, S. 240; c) W. M. Weigert, H. Delle, G. Käbisch, in ‘Wasserstoffperoxid und seine Derivate –
Chemie und Anwendung’, Hüthig, Heidelberg, 1978, Kap. I, S. 9.
[34] M. Hesse, H. Meier, B. Zeeh, in ‘Spektroskopische Methoden in der organischen Chemie’, 6. Aufl.,
Thieme, Stuttgart, New York, 2002, S. 124, Tab. 3.18.