In sharp contrast to the well‐established transition metal‐catalyzed allylic substitution
reactions, the study of the corresponding propargylic substitution reactions has been quite …

Nucleophilic displacement of the propargylic alcohol is one of the sought-after methods in
the current scenario. The highly nucleophilic alkyne functional moiety along with its …

The development of the transition‐metal‐catalyzed propargylic substitution of propargylic
alcohol derivatives is one of the active research subjects in organic synthesis. In this …

Besides being a versatile entity for further chemical transformations, the propargylic subunit
is also part of various natural products, fine chemicals, and synthetic pharmaceuticals …

Iodine has been attracting much attention since its discovery in 1811. It is the weakest
oxidizer among the halogens and a poor electrophile that often needs the assistance of a …

An efficient and regioselective alkenylation of azaheterocycle N-oxides with alkenes
catalyzed by iodine under metal-and external oxidant-free reaction conditions has been …

A variety of chiral binaphthyl-based terminal-alkene-phosphine hybrid ligands were
synthesized in four steps with (S)-BINOL as a starting material and utilized for the Pd …

Inhibition of α-glucosidase is one of the important approaches in designing antidiabetic
drugs for its role in decrease of the carbohydrates digestion to avoid post-prandial increase …

An efficient method for intermolecular hydroarylation of aryl and aliphatic alkenes with
indoles using a combination of [(PR3) AuCl]/AgOTf as catalyst under thermal and microwave …

A palladium-catalyzed asymmetric allylic alkylation of 3-substituted indoles using P/olefin
ligands was successfully achieved to afford a variety of indolenines containing a quaternary …