Copper (I)-catalyzed 1, 3-dipolar cycloaddition between organic azides and terminal
alkynes, commonly known as CuAAC or click chemistry, has been identified as one of the …

The preparation, structure, and chemistry of hypervalent iodine compounds are reviewed
with emphasis on their synthetic application. Compounds of iodine possess reactivity similar …

Cu (I)-catalyzed azide–alkyne 1, 3-dipolar cycloaddition (CuAAC), popularly known as the
“click reaction”, serves as the most potent and highly dependable tool for facile construction …

This review discusses the origins of iodine-mediated oxidation catalysis and gives a
comprehensive overview on this young field of research. The focus is set on oxidative C–X …

Organocatalysis provides robust methodology to furnish “greener” routes to polymer
synthesis. However, the application toward the synthesis of aromatic polymers via step …

Significance: Barbas and co-workers report an organocatalytic cross-coupling reaction of
aldehydes with N-hydroxyimide, hexafluoroisopropyl alcohol, and sulfonimides using n …

Direct methods of carbon‐heteroatom bond formation through functionalization of non‐
reactive C–H bonds represent an attractive approach to the synthesis of interesting products …

CH activation involves any of a wide range of techniques, often using catalysts in which a
carbon to hydrogen covalent bond of an organic compound is cleaved to replace the …

The formation of amide bonds is one of the most stimulating emerging areas in organic and
medicinal chemistry. Amides are recognized as central building blocks in a plethora of …

There is an increasing demand for significant amount of carbohydrate‐containing molecules
owing to their complete chemical, biological, and pharmacological investigations to better …