Iterative click reactions using trivalent platforms for sequential molecular assembly

Gaku Orimoto, Suguru Yoshida

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

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 languageEnglish
Pages (from-to)5824-5827
Number of pages4
JournalChemical Communications
Volume60
Issue number45
DOIs
Publication statusPublished - 9 May 2024

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