Epoxides as intermediates in organic rea
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D.C. Kleinfelter; J.H. Long
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Article
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1969
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Elsevier Science
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French
β 190 KB
Kleinfelter and Dye(l) reported that the rearrangement of 2-E-anisylnorbornane-2,3cis-exo-dial(I) in cone. 82SO4 at 0' gave 40-50% yield of 3-endo-p-anisyl-2-norbomanone(I1). .--Since this yield was an optimum percentage (generally cit. 25% was obtained) we attempted improvement by employing other s