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Pure Appl. Chem., 1998, Vol. 70, No. 8, pp. 1477-1485

http://dx.doi.org/10.1351/pac199870081477

Some aspects of asymmetric catalysis with chiral ferrocenyl ligands

A. Togni, Romano Dorta, C. Köllner and G. Pioda

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  • Drusan Michal, Šebesta Radovan: Enantioselective C–C and C–heteroatom bond forming reactions using chiral ferrocene catalysts. Tetrahedron 2014, 70, 759. <http://dx.doi.org/10.1016/j.tet.2013.11.012>
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  • Togni Antonio, Dorta Romano, Kollner Christoph, Pioda Giorgio: ChemInform Abstract: Some New Aspects of Asymmetric Catalysis with Chiral Ferrocenyl Ligands. ChemInform 2010, 30, no. <http://dx.doi.org/10.1002/chin.199925269>
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  • Lyubimov Sergey E., Davankov Vadim A., Loim Nikolay M., Popova Lyudmila N., Petrovskii Pavel V., Valetskii Petr M., Gavrilov Konstantin N.: Cymantrene-derived monodentate phosphites: New ligands for Rh-catalyzed enantioselective hydrogenation. J Organomet Chem 2006, 691, 5980. <http://dx.doi.org/10.1016/j.jorganchem.2006.08.027>
  • Patti Angela, Pedotti Sonia: Chemoenzymatic access to all four enantiopure stereoisomers of 1-ferrocenyl-1,3-butanediol. Tet Asymm 2006, 17, 778. <http://dx.doi.org/10.1016/j.tetasy.2006.01.028>
  • Herberich Gerhard E., Englert Ulli, Wirth Tobias: Enantiopure Ruthenocenes Cp*Ru(1,2-C5H3R1R2) with a Planar Chiral Cyclopentadienyl Ligand and a Pentamethylcyclopentadienyl Spectator Ligand. Eur J Inorg Chem 2005, 2005, 4924. <http://dx.doi.org/10.1002/ejic.200500686>
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  • Vukićević Mirjana D., Wurst Klaus, Müller Adrian G., Laus Gerhard, Vukićević Rastko D.: Syntheses and crystal structures of (E)/(Z)-isomers of 1-ferrocenyl-1-hydroxyimino-3-thiabutane and 1-ferrocenyl-1-hydroxyimino-4-thiapentane. J Polyhedron 2005, 24, 533. <http://dx.doi.org/10.1016/j.poly.2004.12.013>
  • Gavrilov Konstantin N., Tsarev Vasily N., Konkin Stanislav I., Loim Nikolay M., Petrovskii Pavel V., Kelbyscheva Elena S., Korlyukov Alexander A., Antipin Mikhail Yu., Davankov Vadim A.: Cymantrene-based iminodiamidophosphites: the first phosphite-type ligands with planar chirality. Tet Asymm 2005, 16, 3224. <http://dx.doi.org/10.1016/j.tetasy.2005.08.029>
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  • Plażuk Damian, Zakrzewski Janusz: Acylation of Ferrocene and a 1,1′‐Diphosphaferrocene with Acyl Trifluoroacetates in the Presence of Trifluoromethanesulfonic (Triflic) Acid or Some Metal Triflates. Synth Common 2004, 34, 99. <http://dx.doi.org/10.1081/SCC-120027243>
  • Kloetzing Ralf J., Lotz Matthias, Knochel Paul: New P,N-ferrocenyl ligands for rhodium-catalyzed hydroboration and palladium-catalyzed allylic alkylation. Tet Asymm 2003, 14, 255. <http://dx.doi.org/10.1016/S0957-4166(02)00827-3>
  • Gavrilov Konstantin N., Bondarev Oleg G., Lebedev Roman V., Shiryaev Alexei A., Lyubimov Sergey E., Polosukhin Alexei I., Grintselev-Knyazev Gennady V., Lyssenko Konstantin A., Moiseev Sergey K., Ikonnikov Nikolay S.: Easily Accessible ChiralP,N-Bidentate Aryl Phosphites, Their Complexation and Application in Enantioselective Allylic Alkylation, Sulfonylation and Hydrosilylation. Eur J Inorg Chem 2002, 2002, 1367. <http://dx.doi.org/10.1002/1099-0682(200206)2002:6<1367::AID-EJIC1367>3.0.CO;2-F>
  • Saluzzo Christine, Breuzard Jérémy, Pellet-Rostaing Stéphane, Vallet Martial, Le Guyader Frédéric, Lemaire Marc: New P,N ligands with chiral nitrogen center: applications in homogeneous catalysis. J Organomet Chem 2002, 643-644, 98. <http://dx.doi.org/10.1016/S0022-328X(01)01148-2>
  • Gavrilov K.N, Bondarev O.G, Lebedev R.V, Polosukhin A.I, Shyryaev A.A, Lyubimov S.E, Petrovskii P.V, Moiseev S.K, Kalinin V.N, Ikonnikov N.S: New amino-, imino- and oxazolinophosphites based on 1,1′-bi-2-naphtol: coordination and catalytic properties. J Organomet Chem 2002, 655, 204. <http://dx.doi.org/10.1016/S0022-328X(02)01561-9>
  • Polosukhin A.I, Gavrilov K.N, Bondarev O.G, Korostylev A.V, Petrovskii P.V, Davankov V.A: Quincoridine-based aminophosphite ligands and their Rh(I) and Pd(II) complexes. J Organomet Chem 2000, 608, 89. <http://dx.doi.org/10.1016/S0022-328X(00)00373-9>
  • Gavrilov Konstantin N, Polosukhin Aleksei I: Chiral P,N-bidentate ligands in coordination chemistry and organic catalysis involving rhodium and palladium. RUSS CHEM REV 2000, 69, 661. <http://dx.doi.org/10.1070/RC2000v069n08ABEH000559>