Glycosylated Diarylmethyloxy-Triazines: Facile Synthesis and Aqueous Self-Assembly for Supramolecular Hydrogel Formation
- 12 October 2026
- journal article
- Published by American Chemical Society (ACS) in Bioconjugate Chemistry
- Vol. 37 (10) , 1949-1956
Abstract
Glycosylated self-assembling molecules enable the construction of nanostructures whose surfaces are decorated with saccharides under aqueous conditions, reminiscent of biological systems at both the molecular and cellular levels. Such glyco-nanostructures thus hold great promise as soft materials for biological applications. Herein, we report the facile synthesis of glycosylated diarylmethyloxy-triazines, which serve as new building blocks for fabricating self-assembled nanostructures in aqueous media and forming supramolecular hydrogels. The triazine scaffold enables the protecting-group-free synthesis of glycosylated compounds with reasonable β-anomer selectivity. Notably, both the substituents on the aryl groups attached to the triazine core and the geometry of the glycosidic linkages in the disaccharides strongly influence the hydrogelation behavior.Keywords
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Funding Information
- Support for Pioneering Research Initiated by the Next Generation
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Society for the Promotion of Science (23H01815)
- Japan Society for the Promotion of Science (24H01126)
- Japan Society for the Promotion of Science (25K18078)
- Tokai Pathways to Global Excellence
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