Direct Synthesis of Boron-Protected Alkenyl- and Alkylborons via Copper-Catalyzed Formal Hydroboration of Alkynes and Alkenes was written by Yoshida, Hiroto;Takemoto, Yuki;Takaki, Ken. And the article was included in Asian Journal of Organic Chemistry in 2014.Application of 1214264-88-6 This article mentions the following:
Formal hydroboration of internal alkynes proceeds regio- and stereoselectively by the use of a diboron reagent masked with 1,8-diaminonaphthalene (dan) in the presence of readily available [(Ph3P)3CuCl], leading to direct formation of diverse B-protected alkenylborons in high yield. The B(dan) moiety can also be efficiently installed into the C-C double bond of alkenes to afford the resp. alkylborons. In the experiment, the researchers used many compounds, for example, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6Application of 1214264-88-6).
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application of 1214264-88-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts