Cancer is one of the leading causes of death worldwide. This review highlights the
importance of metal-catalyzed azide–alkyne cycloaddition reactions in the synthesis of …

Highlights•Metabolic procedures of a nucleoside anticancer drug are summarized.•
Anticancer properties of newly synthesized nucleoside analogs are introduced.•Synthetic …

Ferrocidiphenols possessing appropriate substituents in the aliphatic chain have very
promising anticancer properties, but a systematic approach to deciphering their diversified …

Aluminium is useful in various industrial applications and pharmaceuticals but its excess can
pose serious health risks. There lies a need for the development of simple, cost-effective …

A new series of hydrazones tethered 1, 4-disubstituted 1, 2, 3-triazoles have been
synthesized from novel N-substituted alkynes derived from benzohydrazides and benzyl …

Ruthenium (II) complexes with a three-legged piano-stool structure based on an arene ring,
an N-heterocyclic carbene (NHC)-carbene ligand with a peracetylated glucose moiety and …

The triazole functional group plays a pivotal role in the composition of biomolecules with
potent anticancer activities, including numerous clinically approved drugs. The strategic …

The first-in-class luminescent dinucleoside phosphate analogs with a [Re2 (μ-Cl) 2 (CO) 6 (μ-
pyridazine)]“click” linker as a replacement for the natural phosphate group are reported …

CuAAC (Cu catalyzed azide-alkyne cycloaddition) click-reaction is a simple and powerful
method for the post-synthetic modification of organometallic complexes of transition metals …

Conjugation of organometallic entities to drug molecules is a strategy that often results in
products with new biological activity profiles compared to those of their progenitors. In this …