71031-40-8Relevant academic research and scientific papers
Process for preparing 2,2'-bis(diphenylphosphinylmethyl)-1,1'-binaphthyls and new compounds from this class of substances
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, (2008/06/13)
The present invention relates to a process for preparing 2,2'-bis(diphenylphosphinylmethyl)-1,1'-binaphthyls by reacting a reaction mixture prepared in a solvent by reaction of 2,2'-dimethyl-1,1'-binaphthyl with a brominating agent to produce a mixture co
IX. Mono- and biphasic asymmetric hydroformylation with rhodium catalysts of the diphosphine ligand NAPHOS and its sulfonated derivatives
Eckl, Robert W.,Priermeier, Thomas,Herrmann, Wolfgang A.
, p. 243 - 249 (2007/10/03)
Both enantiomers of the diphosphine 2,2′-bis(diphenylphosphinomethyl)-1,1′-binaphthyl NAPHOS were prepared by resolution of the racemic P,P′-dioxide and subsequently applied in the rhodium-catalyzed, asymmetric hydroformylation of styrene. Optically active, highly water-soluble derivatives BINAS were prepared by direct sulfonation of the enantiopure diphosphine NAPHOS and applied in aqueous/organic, two-phase hydroformylation of styrene. The catalytically active rhodium complexes HRh(CO)2(P-P) of both NAPHOS and BINAS were prepared and characterized by infrared and NMR spectroscopy. Optical yields are lower in two-phase hydroformylation compared with the conventional single-phase (organic solvent) technique.
