The strong electron-donation and the steric bulk of trialkylphosphines renders them as very
useful ligands for palladium-catalyzed cross coupling reactions. This critical review reports …

Highly efficient two-step synthesis of ( Z )-2-halo-1-iodoalkenes from terminal alkynes -
Chemical Communications (RSC Publishing) DOI:10.1039/C0CC02156C Royal Society of …

The solvent-free Horner–Wadsworth–Emmons reaction of triethyl phosphonoacetate with a
variety of aldehydes was catalyzed by DBU in the presence of K2CO3 to give E-α, β …

Our recent research efforts identified racemic RC‐33 as a potent and metabolically stable σ1
receptor agonist. Herein we describe the isolation of pure RC‐33 enantiomers by chiral …

Exclusively α-and highly E/Z-selective hydroalkylation of ynone, ynoate, and ynamide was
achieved via photoredox mediated Ni/Ir dual catalysis with high atom and step economy …

The first Pd-catalyzed multicomponent reaction of aryl iodides, alkenyl bromides, and
strained alkenes has been developed, which allowed us to synthesize a variety of …

The highly enantioselective copper (I)/N-heterocyclic carbene (NHC) catalyzed synthesis of
di-and triarylated all-carbon quaternary stereocenters via asymmetric allylic arylation (AAAr) …

We have devised a modular construction of electron-rich alkene derivatives from
trichloroethylene (TCE). The three C− Cl bonds of TCE have sufficiently different reactivities …

In this study we addressed the role of chirality in the biological activity of RC-33, recently
studied by us in its racemic form. An asymmetric synthesis procedure was the first …

Abstract Suzuki coupling of 2-bromo-1, 3-dienes with various boronic acids proceeds with
retention or inversion of configuration of the Br-bearing double bond depending on the …