Deamination of endo- and exo-bornylamines and related reactions
作者:D. V. Banthorpe、D. G. Morris、C. A. Bunton
DOI:10.1039/j29710000687
日期:——
Deamination of the epimeric bornylamines with sodium nitrite–acetic acid mainly gave rearranged products with the isocamphane skeleton but the endo-isomer uniquely formed 7% of monocyclic products. Acetolysis of ethereal diazocamphane and decomposition of N-acetyl-N-nitroso-endo-bornylamine in ethereal acetic acid formed 2% and none of the latter products, respectively. The last two reactions gave