hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides
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Protonation of typical unstrained amides and lactams is heavily favored at oxygen. In contrast, protonation of the highly… Expand THE SITE OF PROTONATION OF A DISTORTED BICYCLIC LACTAM: NITROGEN VS. OXYGEN By Brian T. Sliter University of New Hampshire… Expand N-methylpyperazinyl amides of betulinic, platanic, glycyrrhetic, oleanolic, ursolic, and moronic acids were synthesized and… Expand This dissertation first describes a new method for the formation of a-aryl lactams based on the Vicarious Nucleophilic… Expand Ce procede permet de produire des derives amides representes par la formule generale ci-dessous [XV] ou leurs enantiomeres, de… Expand Infrared investigations on the v(NH) and v(C = N) vibrations of N,N'-disubstituted formamidines, acetamidines and benzamidines… Expand The synthesis of new conjugates with inhibitory action on tumour growth is investigated by linking amino functions of proteins… Expand The wider variety of photcchenical reactions observed for cyclic dicarbximides, rather than for carbxanides, is associated in… Expand