Related Experiment Video
Updated: Jun 6, 2025
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
Asymmetric Synthesis of P-Chirogenic Ferrocenyl BiphePFc* Diphosphine by Ephedrine-Aryne Methods and Application in
Jérôme Bayardon1, Utpal Das1, Yoann Rousselin1
1Université de Bourgogne, UFR des Sciences et Techniques, ICMUB UMR-CNRS 6302, BP 47870, 21078 Dijon Cedex, France.
Abstract:
Chiral diphosphines with a biphenyl bridge and the chirality borne by the phosphorus atoms and not due to the atropoisomery of the biaryl backbone have been scarcely studied. Herein, we report the asymmetric synthesis of the (S,S)-2,2'-bis(ferrocenylphenylphosphino)biphenyl (BiphePFc*) ligand and its application in Rh-catalyzed hydrogenation. The synthesis was based on the enantioselective preparation of P-chirogenic ferrocenyl(o-bromophenyl)phenylphosphine by the reaction of sec-phosphine-borane with 1,2-dibromobenzene and its homocoupling into BiphePFc*. Hydrogenations catalyzed by the Rh/BiphePFc* complex led to enantioselectivities of ≤96%.
More Related Videos
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
07:07Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
Preparation of Alkynes: Dehydrohalogenation
Alkynes can be prepared by dehydrohalogenation of vicinal or geminal dihalides in the presence of a strong base like sodium amide in liquid ammonia. The reaction proceeds with the loss of two equivalents of hydrogen halide (HX) via two successive E2 elimination reactions.
Prochirality
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry