Propargyl alcohols are widely used in organic reactions. Their great success is rooted in the
presence of multiple functional groups. This review will focus on six types of mechanisms:(i) …

This review focuses on providing comprehensive highlights of the recent synthetic pathways
of imidazo [1, 2‐a] pyridines, assisted through transition metal‐catalyzed reactions, multi …

This review describes the efforts in the synthesis of pyrrole derivatives using the reaction of
alkynes with nitrogen‐compounds under transition metal‐catalyzed and metal‐free …

An anti-carbonickelative cyclization via reversible alkenylnickel E/Z isomerization of 2-azido
phenyl propargyl alcohols with aryl boronic acids is achieved using Ni (acac) 2 as the …

Furans are five-membered aromatic heterocycles containing one oxygen atom that are
important building blocks in organic chemistry, but also as natural products found in various …

[4+ 2] oxidative Diels–Alder reaction of readily available alkynols with maleimide is achieved
for the rapid access of pthalimide-fused multicyclic compounds. The reaction is proposed to …

A regio-and stereoselective thiocyanate addition to ynones is achieved using KSCN in
AcOH at 70° C. The reaction is extendable to ynals, ynesulfones, ynoic acids and ynoates …

Addition of arylboronic acids to directing group tethered acetylenes in a regio and
stereoselective manner using an inexpensive catalytic system is achieved for the first time to …

The stereoselective E‐iodosulfonylation of internal alkynes for synthesizing highly defined
tetrasubstituted olefins using sodium phenyl sulfinate and iodine has been achieved. Most of …

The natural occurrence of amides and their unique roles in synthetic materials and
biologically active compounds make amide synthesis one of the most routinely performed …