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Collect. Czech. Chem. Commun. 2000, 65, 717-728
https://doi.org/10.1135/cccc20000717

Diferrocenylphosphine: A Facile Synthesis and Its Use to Prepare Chiral Phosphines

Denis Guillaneux, Lars Martiny and Henri B. Kagan*

Laboratoire de Synthèse Asymétrique (UPRESA 8075), Université Paris-Sud, 91405-Orsay, France

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  • Enomoto Yuuki, Ichiryu Hiroki, Hu Hao, Ura Yasuyuki, Ogasawara Masamichi: C1-Symmetric Binap Derivative Featuring Single Diferrocenylphosphino-Donor Moiety. Organometallics 2021, 40, 1020. <https://doi.org/10.1021/acs.organomet.1c00132>
  • Lemouzy Sébastien, Nguyen Duc Hanh, Gatineau David, Giordano Laurent, Hérault Damien, Buono Gérard: Mechanistic aspects of the stereospecific reduction of chiral hydroxyalkyl phosphinates and phosphine oxides. Pure and Applied Chemistry 2016, 88, 333. <https://doi.org/10.1515/pac-2016-0103>
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  • Kromm Klemenz, Eichenseher Sandra, Prommesberger Markus, Hampel Frank, Gladysz J. A.: Synthesis and Reactivity of 1,2‐ and 1,3‐Diphosphanes that Contain Four Chiral Rhenium Fragments: Architecturally Novel Tetrametallo‐DMPE and ‐DMPP Species that are Unprivileged Ligands for Enantioselective Catalysis. Eur J Inorg Chem 2005, 2005, 2983. <https://doi.org/10.1002/ejic.200500254>
  • Diéguez Montserrat, Pàmies Oscar, Ruiz Aurora, Dı́az Yolanda, Castillón Sergio, Claver Carmen: Carbohydrate derivative ligands in asymmetric catalysis. Coord Chem Rev - 2004, 248, 2165. <https://doi.org/10.1016/j.ccr.2004.04.009>
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  • Kagan Henri B: Various aspects of the reaction of a chiral catalyst or reagent with a racemic or enantiopure substrate. Tetrahedron 2001, 57, 2449. <https://doi.org/10.1016/S0040-4020(01)00065-5>
  • Guillaneux Denis, Martiny Lars, Kagan Henri B.: ChemInform Abstract: Diferrocenylphosphine: A Facile Synthesis and Its Use to Prepare Chiral Phosphines. ChemInform 2000, 31. <https://doi.org/10.1002/chin.200039159>