2015-12-04T10:43:32Z
2015-10-02
2015-12-04T10:43:32Z
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.
Article
Published version
English
Hidròlisi; Lligands; Catàlisi asimètrica; Compostos de bor; Hydrolysis; Ligands; Enantioselective catalysis; Boron compounds
Royal Society of Chemistry
Reproducció del document publicat a: http://dx.doi.org/10.1039/c5cc07504a
Chemical Communications, 2015, vol. 51, p. 17548-17551
http://dx.doi.org/10.1039/c5cc07504a
cc by (c) Orgué Gassol, Sílvia et al., 2015
http://creativecommons.org/licenses/by/3.0/es/