《Aliphatic Oxaboroles Enabling Remarkable Recognition of Diols》 was written by Arakawa, Nozomi; Nagao, Kazunori; Murakami, Ryo; Sumida, Yuto; Arakawa, Hiroshi; Inagaki, Fuyuhiko; Ohmiya, Hirohisa. Quality Control of Bis[(pinacolato)boryl]methane And the article was included in Bulletin of the Chemical Society of Japan in 2020. The article conveys some information:
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. In the experiment, the researchers used many compounds, for example, Bis[(pinacolato)boryl]methane(cas: 78782-17-9Quality Control of Bis[(pinacolato)boryl]methane)
Bis[(pinacolato)boryl]methane(cas: 78782-17-9) belongs to organoboron compounds.Quality Control of Bis[(pinacolato)boryl]methane Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. This stems from their ease of preparation combined with their ability to undergo a broad range of chemical transformations.
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