Flores-Gaspar, AreliOrgué Gassol, SílviaGrabulosa, ArnaldRiera i Escalé, AntoniVerdaguer i Espaulella, Xavier2017-03-142017-03-142014-12-221359-7345https://hdl.handle.net/2445/108386In non-coordinating solvents, borane was shown to be an efficient directing group for the stereoselective 1,2-addition of organolithium reagents to P-stereogenic N-phosphanylimines. Selectivity was reversed in coordinating solvents. This process can lead to novel ligand scaffolds for asymmetric catalysis.4 p.application/pdfeng(c) Flores-Gaspar, Areli et al., 2014Compostos organometàl·licsLligands (Bioquímica)Catàlisi asimètricaOrganometallic compoundsLigands (Biochemistry)Enantioselective catalysisBorane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanyliminesinfo:eu-repo/semantics/article6461262017-03-14info:eu-repo/semantics/openAccess