Journal
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
Volume 93, Issue 4, Pages 576-580Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/bcsj.20200007
Keywords
Oxaborole; Recognition; Sugar
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Funding
- Kanazawa University SAKIGAKE project 2018
- Takeda Science Foundation
- [19K21126]
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5-Membered ring aliphatic oxaboroles revealed unique characteristics in their reactivity with diols. The aliphatic oxaborole derivatives exhibited a higher complexation activity for Alizarin Red S than phenyl-, alkylboronic acid, benzoxaborole, and oxaborin. Furthermore, the sugar recognition ability depended on the chirality of the aliphatic boroles.
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