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M. B. Rubin, unpublished results.
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For reviews of the di-π- and oxadi-π-methane reactions see: S. Hixon, P. S. Mariano, H. E. Zimmerman, Chem Rev. 1973, 73, 531-551; W. G. Dauben, G. Lodder, J. Ipaktschi, Top. Curr. Chem. 1975, 54, 73-114; K. N. Houk, Chem. Rev. 1976, 76, 1-74; K. Schaffner, Tetrahedron 1976, 32, 73-77; M. Demuth in Organic Photochemistry (Ed.: A. Padwa), Dekker, NY, 1991, vol. 11, chapter 2.
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33847798169
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For reviews of the di-π- and oxadi-π-methane reactions see: S. Hixon, P. S. Mariano, H. E. Zimmerman, Chem Rev. 1973, 73, 531-551; W. G. Dauben, G. Lodder, J. Ipaktschi, Top. Curr. Chem. 1975, 54, 73-114; K. N. Houk, Chem. Rev. 1976, 76, 1-74; K. Schaffner, Tetrahedron 1976, 32, 73-77; M. Demuth in Organic Photochemistry (Ed.: A. Padwa), Dekker, NY, 1991, vol. 11, chapter 2.
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For reviews of the di-π- and oxadi-π-methane reactions see: S. Hixon, P. S. Mariano, H. E. Zimmerman, Chem Rev. 1973, 73, 531-551; W. G. Dauben, G. Lodder, J. Ipaktschi, Top. Curr. Chem. 1975, 54, 73-114; K. N. Houk, Chem. Rev. 1976, 76, 1-74; K. Schaffner, Tetrahedron 1976, 32, 73-77; M. Demuth in Organic Photochemistry (Ed.: A. Padwa), Dekker, NY, 1991, vol. 11, chapter 2.
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2842560023
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Photolysis of 7 in MCH at 436 nm at temperatures down to -190°C afforded benzene with no evidence for the formation of a cyclobutanedione intermediate: M. B. Rubin, unpublished results.
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2842539966
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This solvent mixture was used so that 11 would not crystallize from solution at -30°C.
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