The hydroamination of alkenes, dienes, allenes, and alkynes by early transition metal
catalysts has seen significant progress over the last decade, especially with respect to …

The hydroamination of unsaturated carbon‐carbon linkages allows a facile and highly atom‐
economical access to industrially relevant nitrogen‐containing basic and fine chemicals as …

This short review highlights recent catalyst developments from group 3–5 elements reported
in the past few years to promote two highly atom-saving transformations, namely …

This Perspective article outlines some of the recent advancements completed in the
development of (chiral) metal-free and late-transition metal catalysts for the inter-and …

Metal-catalyzed hydroamination, a direct and atom-economic approach for the formation of
CÀN bonds, is becoming an increasingly powerful method in organic synthesis.[1] This …

Hydroamination is a highly atom-economical process in which an amine N–H functionality is
added to an unsaturated carbon–carbon linkage. This potentially highly useful process gives …

Conspectus Catalytic intermolecular hydroamination of alkenes is an atom-and step-
economical method for the synthesis of amines, which have important applications as …

The selective and asymmetric addition of amines across alkene C= C bonds
(hydroamination of alkenes) is one of the most important tool to synthesise chiral amines …

Asymmetric intramolecular hydroamination reaction is a stately way to prepare chiral
nitrogen-containing heterocyclic compounds. We report in this account our personal …

Amidate ligands have been used as a modular ligand set for early transition‐metal
complexes, and have been found to exhibit high reactivity in the catalytic hydroamination of …