Stereospecific SN2@P reactions: Novel access to bulky P-stereogenic ligands

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Abstract

The stereospecific hydrolysis of bulky aminophosphine boranes is reported for the first time. The resulting phosphinous acid boranes, upon activation, undergo stereospecific nucleophilic substitution reaction at the phosphorous center with amine nucleophiles. The combination of these two processes provides a novel access to bulky P∗-ligands.

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Orgué, S., Flores-Gaspar, A., Biosca, M., Pàmies, O., Diéguez, M., Riera, A., & Verdaguer, X. (2015). Stereospecific SN2@P reactions: Novel access to bulky P-stereogenic ligands. Chemical Communications, 51(99), 17548–17551. https://doi.org/10.1039/c5cc07504a

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