Transition-metal catalyzed reactions that are able to construct complex aliphatic amines from
simple, readily available feedstocks have become a cornerstone of modern synthetic …

Hydroformylation is the addition of synthesis gas (“syngas”), a mixture of CO and H2, to
olefins in the presence of a catalyst under the formation of aldehydes. Hydrogen (“hydro”) …

In the context of atom economy and low environmental impact, synthesis of amines by an
efficient catalytic process is of great importance to produce these building blocks for fine …

Carbon–carbon coupling catalyzed by transition metals represents a powerful synthetic
method to have an access to organic molecules, especially when they present a significant …

Under the conditions of ruthenium catalyzed transfer hydrogenation using 2-propanol as
terminal reductant, 1, 3-dienes engage in reductive C–C coupling with formaldimines …

Ruthenium (II)‐catalyzed hydrogen transfer from 2‐propanol mediates reductive coupling of
1, 1‐disubstituted allenes with formaldimines with complete branch‐regioselectivity, thus …

A convenient, general, and high yielding Pd-catalyzed cross-coupling of
methanesulfonamide with aryl bromides and chlorides is reported. The use of this method …

Hydroaminomethylation is a perfect reaction for converting alkenes into valuable amines
with high atom economy in the presence of the syngas and amines. Significant progress has …

The design and catalytic implementation of tandem reactions to selectively create nitrogen-
containing products under mild conditions has encountered numerous challenges in …

An efficient and regioselective ruthenium-catalyzed hydroaminomethlyation of olefins is
reported. Key to success is the use of specific 2-phosphino-substituted imidazole ligands …