Mechanism of C(8)-bromination of 3,3-dibromocamphor
Abstract
Investigation of the mechanism of C(8)-bromination of 3,3-dibromocamphor using deuterium-labelled precursors indicates that the process may involve 2,3-endo-methyl shifts.
Investigation of the mechanism of C(8)-bromination of 3,3-dibromocamphor using deuterium-labelled precursors indicates that the process may involve 2,3-endo-methyl shifts.
W. M. Dadson and T. Money, J. Chem. Soc., Chem. Commun., 1982, 112 DOI: 10.1039/C39820000112
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