Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst
C. Liana Allen, Benjamin N. Atkinson, Jonathan M. J. Williams
Abstract
C. Liana Allen, Benjamin N. Atkinson, Jonathan M. J. Williams
Abstract
Metal-free catalysis: A method for the transamidation of primary amides with primary or secondary amines provides access to secondary and tertiary amides, by utilizing catalytic quantities of hydroxylamine hydrochloride to activate the chemically robust primary amide group (see scheme). A mechanism of primary amide activation through a hydrogen-bonding complex is proposed.
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Metal-free catalysis: A method for the transamidation of primary amides with primary or secondary amines provides access to secondary and tertiary amides, by utilizing catalytic quantities of hydroxylamine hydrochloride to activate the chemically robust primary amide group (see scheme). A mechanism of primary amide activation through a hydrogen-bonding complex is proposed.
Key concepts: Primary (astronomy), Amide, Hydroxylamine, Catalysis, Hydroxylamine Hydrochloride, Chemistry, Hydrochloride, Organic chemistry