64091-23-2Relevant articles and documents
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.
Process for preparing tertiary diarylalkylphosphines
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, (2008/06/13)
The invention relates to a process for preparing phosphines STR1 where, for example R1 is (C1 -C10)alkyl, (C3 -C10)cycloalkyl, C(YZ)aryl Y, Z is (C1 -C4)alkyl, hydrogen, Aryl is