Explore: Amination

In organic chemistry, the Buchwald–Hartwig amination is a chemical reaction for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed coupling

Reductive amination (also known as reductive alkylation) is a form of amination that converts a carbonyl group to an amine via an intermediate imine.

Amination is the process by which an amine group is introduced into an organic molecule. This type of reaction is important because organonitrogen compounds

Transamination is a chemical reaction that transfers an amino group. In biochemistry, the processor occurs extensively during amino acid synthesis, catalyzed

Electrophilic amination is a chemical process involving the formation of a carbon–nitrogen bond through the reaction of a nucleophilic carbanion with

The following is the overall form of the general reaction: The direct amination of pyridine with sodium amide can take place in liquid ammonia or an aprotic

Deamination is the removal of an amino group from a molecule. Enzymes that catalyse this reaction are called deaminases. In the human body, deamination

aldehydes but not most ketones. It is especially suitable for reductive aminations of aldehydes and ketones. However, unlike sodium cyanoborohydride, sodium

aldehydes or ketones to amines. The reaction is an example of reductive amination. The reaction, named after Rudolf Leuckart, uses either ammonium formate

nitrogenous compounds formed mainly by decarboxylation of amino acids or by amination and transamination of aldehydes and ketones. Biogenic amines are organic