Abstract
A highly efficient Cu-catalyzed C-B bond formation has been developed to transform 1-azadienes into β-imino boronate esters when reacted with bis(pinacolato)diboron and a base. A series of functionalized imines and oximes were found to react under very mild conditions. A further oxidation protocol enabled β-iminoalcohols to be selectively synthesized. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
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APA
Sole, C., & Fernández, E. (2009). Catalytic β-boration/oxidation of 1-azadienes. Chemistry - An Asian Journal, 4(12), 1790–1793. https://doi.org/10.1002/asia.200900311
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