The classical heterocoupling of a 1-haloalkyne with a terminal alkyne catalyzed by copper
salts in the presence of a base for the synthesis of unsymmetrical diynes is termed the …

The Cadiot–Chodkiewicz reaction offers an elegant strategy for the formation of 1, 3-diynes
via Cu-catalyzed cross-coupling of alkynyl halides with terminal alkynes in the presence of …

A new and efficient method for the synthesis of unsymmetrical 1, 3‐butadiynes by gold‐
catalyzed C (sp)–C (sp) cross‐coupling of terminal alkynes with alkynyl hypervalent iodine …

A novel visible-light-promoted copper-catalysed process for the Csp–Csp cross-coupling
reaction of terminal alkynes at room temperature is described. The current photochemical …

A photochemical dual‐catalytic cross‐coupling to form alkynyl sulfides via C (sp)− S bond
formation is described. The cross‐coupling of thiols and bromoalkynes is promoted by a …

With the objective to identify novel anticancer leads, herein ruthenium-catalyzed
electrochemical homo-and heterocoupling reactions of terminal alkynes have been …

A mild and benign methodology to syntheses biaryls and 1, 3‐diynes has been
demonstrated using the nickel nanoparticles supported on reduced graphene oxide (RGO …

An iron-based catalytic system was developed for the cross-coupling of 1-bromoalkynes with
terminal alkynes to selectively generate unsymmetrical 1, 3-butadiynes in water under air. It …

Abstract Cobalt (II)‐catalyzed C (sp2) O cross‐coupling between aryl/heteroaryl alcohols
and vinyl/aryl halides in the presence of CuI has been achieved under ligand‐free …

A Pd/Ni-free copper-catalysed tandem synthesis was realized for rapid access to
unsymmetrical 1, 3-diynes from 1, 1-dibromoalkenes and terminal alkynes. This method was …