Synthesis of Pseudo-geminal-, Pseudo-ortho-, and ortho-Phosphinyl-oxazolinyl-[2.2]paracyclophanes for Use as Ligands in Asymmetric Catalysis
Author:
Affiliation:
1. Institut für Organische Chemie der RWTH Aachen, Landoltweg 1, D-52074 Aachen, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo060668h
Reference52 articles.
1. Rozenberg, V.; Sergeeva, E.; Hopf, H. InModern CyclophaneChemistry; Gleiter, R., Hopf, H., Eds.; Wiley-VCH: New York, 2004; p 435.
2. [2.2]Paracyclophane derivatives in asymmetric catalysis
3. The First Structural Characterization of a [2.2]PHANEPHOS−Transition-Metal Complex: Structure of rac-[Pd(4,12-bis(diphenylphosphino)[2.2]paracyclophane)Cl2]
4. [2.2]PHANEPHOS-Ruthenium(II) complexes: Highly active asymmetric catalysts for the hydrogenation of β-ketoesters
5. Kinetic Resolution of rac-4,12-Dibromo[2.2]paracyclophane in a Palladium [2.2]PHANEPHOS Catalyzed Amination
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