A. W. Fort, R. E. Leary
May 1, 1960
Citations
0
Influential Citations
3
Citations
Journal
Journal of the American Chemical Society
Abstract
The diazotization of 3-phenyl-1-butylamine-3-C/sup 14/ in acetic acid gives 3-phenyl-1-butene, 3-phenyl-1-butyl acetate, and diastereoisomeric 3- phenyl-2-butyl acetates. 3-pmixture. The secondary ester products of these reactions show extensive isotope-position rearrangement. The significance of these results is discussed.