Abstract
A facile synthesis of multi(triazole)s by iterative click reactions is disclosed. Good functional group tolerance of sequential click assembly by sulfur-fluoride exchange (SuFEx), copper-catalyzed azide-alkyne cycloaddition (CuAAC), and thia-Michael reaction realizes the iterative click reactions. Diverse multi(triazole)-type mid-molecules can be synthesized easily from readily available modules through good chemoselective reactions without functional group transformation steps.
Original language | English |
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Pages (from-to) | 5824-5827 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 60 |
Issue number | 45 |
DOIs | |
Publication status | Published - 9 May 2024 |