Journal of the Chemical Society. Chemical communications p. 670 - 671 (1981)
Update date:2022-08-11
Topics:
Barluenga, Jose
Jimenez, Carmen
Najera, Carmen
Yus, Miguel
The reaction of olefins with anhydrous mercury(II) nitrate in the presence of primary amides leads, after in situ alkaline sodium borohydride reduction, to the corresponding N-substituted amides; this procedure provides a new, convenient method for the Markovnikov amidation of carbon-carbon double bonds.
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