Abstract
A series of bulky secondary amines were treated with two equiv. Grignard reagent MeMgI at low temperature to yield the corresponding magnesium methyl complexes (1-4) in high yields. The prepared complexes have been comprehensively characterized. All four complexes exhibited very high reactivity as efficient pre-catalysts in the catalytic hydroboration of ketones with pinacolborane under mild conditions and at low catalyst loadings.
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CITATION STYLE
Ma, M., Li, J., Shen, X., Yu, Z., Yao, W., & Pullarkat, S. A. (2017). Sterically bulky amido magnesium methyl complexes: Syntheses, structures and catalysis. RSC Advances, 7(72), 45401–45407. https://doi.org/10.1039/c7ra08836a
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