Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C-O Bond Activation
Marc Magre, Eva Paffenholz, Bholanath Maity, Luigi Cavallo* and Magnus Rueping*
*KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia, Email: luigi.cavallokaust.edu.sa, magnus.ruepingkaust.edu.sa
M. Magre, E. Paffenholz, B. Maity, L. Cavallo, M. Rueping, J. Am. Chem. Soc., 2020, 142, 14286-14294.
DOI: 10.1021/jacs.0c05917
see article for more reactions
Abstract
A readily available magnesium catalyst achieves a selective hydroboration of a wide range of epoxides and oxetanes yielding secondary and tertiary alcohols in excellent yields and regioselectivities.
see article for more examples
While ads financed 62% of the published abstracts in 2024, donations allowed us to publish additional 12%. 26% of the abstracts have been published voluntarly. If you kindly donate, we can publish more freely accessible information and help the chemical community even more:
If you don't like pawalls or a flood of more and more advertising, then you can send a clear signal here!
Key Words
cleavage of ethers, reduction of epoxides, pinacolborane
ID: J48-Y2020