Hydroamination, the addition of an N–H bond across a C–C multiple bond, is a reaction with
a great synthetic potential. Important advances have been made in the last decades …

This Review examines recent developments in late transition metal-catalyzed
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …

Aminium radical cations have been extensively studied as electrophilic aminating species
that readily participate in C–N bond forming processes with alkenes and arenes. However …

Terminal alkenes are readily available functional groups which appear in α‐olefins
produced by the chemical industry, and they appear in the products of many contemporary …

We report here a photocatalytic method for the intermolecular anti-Markovnikov
hydroamination of unactivated olefins with primary alkyl amines to selectively furnish …

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 …

Hydroamination, an atom-economic one-step reaction that refers to the addition of an NH
unit into CC/CX multiple bonds, provides an ideally efficient methodology to construct C–N …

Use of organolanthanides in the catalytic intermolecular hydrophosphination and
hydroamination of multiple C–C bonds - Dalton Transactions (RSC Publishing) DOI:10.1039/C6DT03913H …

Abstract [{N^ N} M (X)(thf) n] alkyl (X= CH (SiMe3) 2) and amide (X= N (SiMe3) 2) complexes
of alkaline earths (M= Ca, Sr, Ba) and divalent rare earths (YbII and EuII) bearing an …

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 …