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The click reaction happened in membrane matrix in bulk.
Notably, modified opioid peptides bearing alkynyl moiety could be further functionalized through well-established click reaction.
The chelating units were connected to the pharmacophore using the click reaction of Huisgen.
The novel (S -BINOL-based S -BINOL-basedporating triazole moietieS -BINOL-basedained by click reaction.
The new compounds (17 40) were synthesized through CuAAC click reaction and SAR analysis carried out.
A subsequent click reaction with the azido-biotin derivative 25 proceeded smoothly to give triazole 26.
We designed and synthesized various peptide dendrimers using a 1,3-dipolar cycloaddition (Click) reaction.
The latter two steps, substitution and click reaction could proceed smoothly in a one-pot process.
Chain extension via click reaction resulted in high molecular weight multiblock copolymers.
The microparticles were prepared through click reaction in aqueous system with the aid of stabilizer.
The final block-brush copolymer was synthesized by the click reaction between these two polymer precursors.
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