| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1347232 | Tetrahedron: Asymmetry | 2014 | 6 Pages |
Phosphine–phosphites 3a and 3b, derived from diphenylhydroxymethyl phosphine have been prepared. From these ligands [Rh(COD)(3a)]BF45a and RuCl2(3b)[(S,S)-DPEN] 6b (DPEN = 1,2-diphenylethylenediamine) were synthesized and their structure determined by X-ray diffraction. Ligands 3 are characterized by a small bite angle of 83°. In addition, 5a led to an active catalyst for the hydrogenation of olefins, giving enantioselectivities of up to 96% ee. Likewise, compound 6b showed good activity and enantioselectivity in the hydrogenation of N-1-phenyl ethylidene aniline and a completed reaction at S/C = 500 in 24 h with 83% ee.
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Diphenylphosphinomethyl-(R)-3,3′-di-tert-butyl-5,5′,6,6′-tetramethyl-1,1′-biphen-2,2′-diyl-phosphiteC38H47O3P2Ee = 100%[α]D20 = −392 (c 1.0, THF)Source of chirality: (S)-3,3′-di-tert-butyl-5,5′,6,6′-tetramethyl-1,1′-biphenyl-2,2′-diolAbsolute configuration: (R)
