Drießen-Hölscher B, Kralik J, Agel F, Steffens C, Hu C (2004)
Publication Language: English
Publication Type: Journal article, Original article
Subtype: other
Publication year: 2004
Publisher: Wiley-VCH Verlag
Book Volume: 346
Pages Range: 979-982
Journal Issue: 8
The authors found a modular route for the synthesis of Cl-MeOBIPHEP ligands (I; R = Ph, p-FC6H4, xylyl, 2-furyl, 2,5-(MeO)2C6H3) via the corresponding biphenol that allows the authors to introduce several substituents without the necessity to sep. the enantiomers of each deriv. These new diphosphines were used to prepn. Ru(I)(O2CCF3)2 for use in the Ru-catalyzed enantioselective hydrogenation of di-Me itaconate with ee values up to 97%. [on SciFinder(R)]
APA:
Drießen-Hölscher, B., Kralik, J., Agel, F., Steffens, C., & Hu, C. (2004). New route to biaryl phosphanes with axial chirality as ligands for enantioselective hydrogenations. Advanced Synthesis & Catalysis, 346(8), 979-982. https://dx.doi.org/10.1002/adsc.200404034
MLA:
Drießen-Hölscher, Birgit, et al. "New route to biaryl phosphanes with axial chirality as ligands for enantioselective hydrogenations." Advanced Synthesis & Catalysis 346.8 (2004): 979-982.
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