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For a review of the area, see R. S. Ward, Chem. Soc. Rev., 1982, 75
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F. E. Ziegler, I. Chliwner, K. W. Fowler, S. J. Kanfer, S. J. Kuo, and N. D. Sinha, J. Am. Chem. Soc., 1980, 102, 790. For a review of the area, see R. S. Ward, Chem. Soc. Rev., 1982, 75.
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0017300335
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The non-phenolic oxidation approach has been used in a number of successful syntheses of steganone
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The non-phenolic oxidation approach has been used in a number of successful syntheses of steganone: A. S. Kende and L. S. Liebeskind, J. Am. Chem. Soc., 1976, 98, 267
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1977, 99, 7082. For isostegane see, R. E. Damon, R. H. Schlessinger, and J. P. Blount, J. Org. Chem
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A. S. Kende, L. S. Liebeskind, J. E. Mills, P. S. Rutledge, and D. P. Curran, J. Am. Chem. Soc., 1977, 99, 7082. For isostegane see, R. E. Damon, R. H. Schlessinger, and J. P. Blount, J. Org. Chem., 1976, 41, 3772.
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