Abstract
Ethyl [(adamantan-1-yl)alkylene(phenylene)amino]oxoacetates and N1,N2-bis[(adamantan-1-yl)-alkylene(phenylene)oxamides were prepared in yields of 72–87 and 18–60%, respectively, by the reaction of amines of the adamantane series with ethyl chlorooxoacetate and oxalyl chloride in methylene chloride in mild conditions.
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