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For examples see: J. D. Ballantyne and P. J. Sykes, J. Chem. Soc. (C), 731 (1970); S. C. Welch, A. S. C. P. Rao, J. T. Lyon and J-M. Assercq, J. Am. Chem. Soc., 105, 252 (1983); W. M. Daniewski, E. Kubak and J. Jurczak, J. Org. Chem., 50, 3963 (1985); K. H Schulte-Elte, W. Giersch, B. Winter, H. Pamingle and G. Ohloff, Helv. Chim. Acta, 68, 1961 (1985); H. Hagiwara and H. Uda, J. Chem. Soc., Chem. Commun., 815 (1988).
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For examples see: J. D. Ballantyne and P. J. Sykes, J. Chem. Soc. (C), 731 (1970); S. C. Welch, A. S. C. P. Rao, J. T. Lyon and J-M. Assercq, J. Am. Chem. Soc., 105, 252 (1983); W. M. Daniewski, E. Kubak and J. Jurczak, J. Org. Chem., 50, 3963 (1985); K. H Schulte-Elte, W. Giersch, B. Winter, H. Pamingle and G. Ohloff, Helv. Chim. Acta, 68, 1961 (1985); H. Hagiwara and H. Uda, J. Chem. Soc., Chem. Commun., 815 (1988).
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For examples see: J. D. Ballantyne and P. J. Sykes, J. Chem. Soc. (C), 731 (1970); S. C. Welch, A. S. C. P. Rao, J. T. Lyon and J-M. Assercq, J. Am. Chem. Soc., 105, 252 (1983); W. M. Daniewski, E. Kubak and J. Jurczak, J. Org. Chem., 50, 3963 (1985); K. H Schulte-Elte, W. Giersch, B. Winter, H. Pamingle and G. Ohloff, Helv. Chim. Acta, 68, 1961 (1985); H. Hagiwara and H. Uda, J. Chem. Soc., Chem. Commun., 815 (1988).
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For examples see: J. D. Ballantyne and P. J. Sykes, J. Chem. Soc. (C), 731 (1970); S. C. Welch, A. S. C. P. Rao, J. T. Lyon and J-M. Assercq, J. Am. Chem. Soc., 105, 252 (1983); W. M. Daniewski, E. Kubak and J. Jurczak, J. Org. Chem., 50, 3963 (1985); K. H Schulte-Elte, W. Giersch, B. Winter, H. Pamingle and G. Ohloff, Helv. Chim. Acta, 68, 1961 (1985); H. Hagiwara and H. Uda, J. Chem. Soc., Chem. Commun., 815 (1988).
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Zwitterionic or pre-epoxide species have been proposed as intermediates in singlet oxygen cycloadditions: T. Linker and L. Frölich, Angew. Chem., Int. Ed. Engl., 33, 1971 (1994); T. Linker and L. Frölich, J. Am. Chem. Soc., 117, 2694 (1995); T. Linker, F. Rebein and G. Tóth, J. Chem. Soc., Chem Commun., 2585 (1996).
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