Chiral phosphorus ligands play a crucial role in asymmetric catalysis for the efficient
synthesis of useful optically active compounds. They are largely categorized into two …

Chiral amines are key structural motifs present in a wide variety of natural products, drugs,
and other biologically active compounds. During the past decade, significant advances have …

Both enantiomers of 2, 3-bis (tert-butylmethylphosphino) quinoxaline (QuinoxP*), 1, 2-bis
(tert-butylmethylphosphino) benzene (BenzP*), and 1, 2-bis (tert-butylmethylphosphino)-4, 5 …

In this account, the design, synthesis, and application of P‐chirogenic phosphine ligands
that have been mainly carried out in our laboratory over the last three decades are …

A N-heterocyclic carbene-catalyzed (NHC) three-component reaction involving N-
aminopyridinium salts, alkenes, and aldehydes for the synthesis of β-amino ketones is …

Chiral amines and their derivates are important building blocks for the synthesis of many
pharmaceutical and biologically active molecules.[1] Methods for preparing chiral aromatic …

MaxPHOS is an active and robust P‐stereogenic ligand for asymmetric catalysis. The
presence of an NH bridge between the two phosphine moieties allows the NH/PH …

A visible light photoredox-catalyzed N-centered radical addition/semipinacol rearrangement
cascade of cycloalkanol-substituted 1H-indenes or styrenes with N-arylsulfonyl protected 1 …

An amidoarylcarbonylation reaction of aromatic aldehydes and olefins with Katritzky
pyridinium salts by N-heterocyclic carbene (NHC)-catalyzed radical relay to construct C–C …

A highly regio‐and enantioselective hydrogenation of challenging tetrasubstituted allenyl
sulfones has been developed, affording chiral allylic sulfones in good yields with excellent …