The carbon− carbon triple bond of alkynes is one of the basic functional groups, its reactions
belonging to the foundations of organic chemistry. In the past decades, acetylene chemistry …

This review article will consider the preparation and application of ynones in synthetic
organic chemistry. Concerning the preparation of these bifunctional compounds, several …

Recent developments concerning the application of polymer supported organometallic
reagents in solid phase synthesis are reviewed, with a special focus on methodology for …

The acyl Sonogashira reaction represents an extension of Sonogashira cross-coupling to
acid chlorides which replace aryl or vinyl halides, while terminal acetylenes are used as …

We have demonstrated a facile one-step synthetic strategy for the preparation of Cu/Cu2O
nanoparticles (NPs) via a microwave method. The microwave energy acts as a driving force …

A novel polystyrene-supported palladium (II) dithizone complex is found to be a highly active
catalyst for the Suzuki, Heck, and Sonogashira reactions of aryl halides in water. By this …

A new polystyrene-anchored Pd (II) phenyldithiocarbazate complex is synthesized and
characterized. This Pd-complex behaves as an efficient heterogeneous catalyst in the Heck …

Supported copper nanoparticles are utilized for the first time as a highly efficient and
reusable catalyst in the coupling of acyl chlorides and terminal alkynes to prepare various …

4-amino-5-methyl-3-thio-1, 2, 4-triazole-functionalized polystyrene resin-supported Pd (II)
complex was found to be an efficient catalyst in the palladium-catalyzed Suzuki–Miyaura …

A polystyrene-supported palladium (II) 1-phenyl-1, 2-propanedione-2-oxime thiosemi-
carbazone (PPDOT) complex is found to be a highly active catalyst for the Sonogashira …