The copper‐catalyzed azide/alkyne cycloaddition reaction (CuAAC) has emerged as the
most useful “click” chemistry. Polymer science has profited enormously from CuAAC by its …

The copper-catalyzed azide–alkyne cycloaddition (CuAAC) is one of the most broadly
applicable and easy-to-handle reactions in the arsenal of organic chemistry. However, the …

True colors: Novel pyrene analogues of Prodan exhibit outstanding photophysical properties
with remarkably high fluorescence quantum yield (QY) in solvents ranging from apolar …

Abstract The use of 'Click Reaction'for Cu (I) catalyzed azide–alkyne cycloaddition (CuAAC)
has emerged as one of the most powerful tools for the synthesis of library of organic …

A new, easy-to-prepare and highly selective pyrene-linked tris-triazole amine fluorescent
chemosensor has been designed from tripropargylamine and pyrene azide using Cu (I) …

We have systematically synthesized 1-, 3-, 6-, and 8-alkyl-substituted pyrene derivatives
using the latest synthesis methods and investigated the effects of alkyl substitution on the …

Recent years has witnessed increasing development and exploitation of fluorescence
techniques which has been spurred by the discovery, design and synthesis of novel …

In this review, we summarize the recent advances in the use of pyrene-modified
oligonucleotides as a platform for functional nucleic acid-based constructs. Pyrene is of …

A broadly applicable catalyst system consisting of water-soluble Pd–imidate complexes has
been enployed for the Suzuki–Miyaura cross-coupling of four different nucleosides in water …

This review highlights the most recent advances in click chemistry associated with DNA. Cu
[I]-catalyzed azides-alkynes Huisgen cycloadditions (CuAAC) and a strain-promoted alkyne …