Issue 12, 2022

Accelerated synthesis of dendrimers by thermal azide–alkyne cycloaddition with internal alkynes

Abstract

An accelerated synthesis of dendrimers is presented by combining the thermal azide–alkyne cycloaddition (AAC) and azide substitution reactions. The strategy is among the most user-friendly, flexible, modular, and accelerated strategies for the synthesis of dendrimers. Despite AAC being an archetypal click reaction that proceeds with complete atom-economy and is amenable to a high chemical diversity, high temperatures and prolonged reaction times have limited its application in the synthesis of dendrimers. By combining the optimized AAC/azide substitution conditions, simplified workups/purifications, and a strict alignment to green chemistry principles, not only a G5 dendrimer with 96 terminal groups has been synthesized and characterized in less than 12 h, but also the newly formed triazol has been successfully used to promote the easy exploration of the dendritic chemical space, the peripheral decoration of dendrimers, and the straightforward adjustment of dendritic properties.

Graphical abstract: Accelerated synthesis of dendrimers by thermal azide–alkyne cycloaddition with internal alkynes

Supplementary files

Article information

Article type
Paper
Submitted
04 fev 2022
Accepted
05 may 2022
First published
13 may 2022

Green Chem., 2022,24, 4897-4901

Accelerated synthesis of dendrimers by thermal azide–alkyne cycloaddition with internal alkynes

S. P. Amaral, J. Correa and E. Fernandez-Megia, Green Chem., 2022, 24, 4897 DOI: 10.1039/D2GC00473A

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