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Epoxides as intermediates in organic reactions. I

โœ Scribed by D.C. Kleinfelter; J.H. Long


Book ID
104239016
Publisher
Elsevier Science
Year
1969
Tongue
French
Weight
190 KB
Volume
10
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


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 solvent systems.known to effect pinacol rearrangements(2):


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