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 …

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 …

The increasing application of positron emission tomography (PET) in nuclear medicine has
stimulated the extensive development of a multitude of novel and versatile bioorthogonal …

Glucose homeostasis plays a key role in numerous fundamental aspects of life, and its
dysregulation is associated with many important diseases such as cancer. The atypical …

Cu (I)-catalyzed click reaction, a set of powerful and virtually reliable 1, 3 dipolar
cycloaddition of organic azide and terminal alkyne, has been extensively used in adjoining …

Click chemistry has received considerable attention as powerful modular synthesis
approach, which has found numerous applications in many areas of modern organic …

A series of 'clickable'mannopyranosides bearing a triflate leaving group at C-2 position were
synthesized and tested for their potential as 18F-labeling precursors. 3, 4, 6-Tri-O-acetyl-2-O …

Due to expanding applications of positron emission tomography (PET) there is a demand for
developing new techniques to introduce fluorine‐18 (t1/2= 109.8 min). Considering that …

Abstract The copper (I)‐catalysed 1, 3‐dipolar cylcoaddition of terminal alkynes with
substituted azides has seen a rapidly growing popularity in a wide range of applications …

A new 18F‐based prosthetic group has been prepared for the labeling of azide‐modified
peptides for use in PET imaging. 2‐[18F] fluoro‐3‐(hex‐5‐ynyloxy) pyridine ([18F] …