Organocatalysis has emerged as one of the most progressive and prevailing field of organic
synthesis to assist green chemistry. Constantly increasing demand of promising scaffolds to …

The present review is devoted to the application of transition metal complexes with such
ligands as amino acids, peptides and carbohydrates in catalysis. The literature published …

The intrinsic heterogeneity of many nanoformulations is currently challenging to characterize
on both the single particle and population level. Therefore, there is great opportunity to …

The glycosyl 1, 2, 3-triazoles are expediently accessible from readily available sugar-
derived glycosyl azide by utilizing modular CuAAC “Click Chemistry”, and the resulting …

We have developed an efficient visible light induced copper‐mediated protocol to
synthesize conjugated 1, 3‐diynes via decarboxylative homocoupling of arylpropiolic acids …

This report describes a convenient method for the Cu (I)-catalyzed Sonogashira cross-
coupling reaction of aryl/heteroaryl halides and alkynyl sugars in the presence of a 1, 2, 3 …

Conjugated diyne derivatives are important scaffolds in modern organic synthetic chemistry.
Using the Glaser reaction involves the coupling of terminal alkynes which can efficiently …

Immediately after the invention of 'Click Chemistry'in 2002, the regioselective 1, 2, 3-triazole
scaffolds resulted from respective organic azides and terminal alkynes under Cu (I) catalysis …

Abstract Regulation of Hybrid Materials of Ministry of Education, Bimetallic nanoclusters with
synergistic effect exhibit better stability and activity than monometallic nanoclusters in …

Abstract A novel organocatalyzed [3+ 2] cycloaddition reaction of nitroolefins with glycosyl
azides as well as organic azides has been developed for successful construction of 1, 5 …