Axial chirality control of gold(biphep) complexes by chiral anions: application to asymmetric catalysis.
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[1] C. Bataille,et al. Enantiomerically pure bicyclo[3.3.1]nona-2,6-diene as the sole source of enantioselectivity in BIPHEP-Rh asymmetric hydrogenation. , 2008, Chemical communications.
[2] S. Kawauchi,et al. Axial chirality control of tropos BIPHEP-Rh complexes by chiral dienes: synergy effect in catalytic asymmetric hydrogenation. , 2008, Chemical communications.
[3] M. Terada. Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon-carbon bond forming reactions. , 2008, Chemical communications.
[4] M. Reetz. Combinatorial transition-metal catalysis: mixing monodentate ligands to control enantio-, diastereo-, and regioselectivity. , 2008, Angewandte Chemie.
[5] M. T. Reetz. Kombinatorische Übergangsmetallkatalyse: Mischungen einzähniger Liganden zur Kontrolle der Enantio-, Diastereo- und Regioselektivität , 2008 .
[6] D. Nakashima,et al. Enantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl ether: the difference between Brønsted and Lewis acid catalysis. , 2008, Angewandte Chemie.
[7] T. Akiyama,et al. Stronger Brønsted acids. , 2007, Chemical reviews.
[8] S. Doherty,et al. Rhodium-catalyzed double [2 + 2 + 2] cycloaddition of 1,4-bis(diphenylphosphinoyl)buta-1,3-diyne with tethered diynes: a modular, highly versatile single-pot synthesis of NU-BIPHEP biaryl diphosphines. , 2007, Organic letters.
[9] Stephen J. Lee,et al. Gold(I)-catalyzed asymmetric cycloisomerization of eneallenes into vinylcyclohexenes. , 2007, Angewandte Chemie.
[10] G. L. Hamilton,et al. A Powerful Chiral Counterion Strategy for Asymmetric Transition Metal Catalysis , 2007, Science.
[11] M. Lautens,et al. New frontiers in asymmetric catalysis , 2007 .
[12] G. Bernardinelli,et al. TRISPHAT-N: A Chiral Hexacoordinated Phosphate Anion with Unique Asymmetric Coordinating Properties , 2007 .
[13] M. Ōki. Recent Advances in Atropisomerism , 2007 .
[14] F. Toste,et al. Gold(I)-catalyzed enantioselective intramolecular hydroamination of allenes. , 2007, Journal of the American Chemical Society.
[15] D. Nakashima,et al. Design of chiral N-triflyl phosphoramide as a strong chiral Brønsted acid and its application to asymmetric Diels-Alder reaction. , 2006, Journal of the American Chemical Society.
[16] K. Mikami,et al. Asymmetric Activation and Deactivation of Racemic Catalysts , 2006 .
[17] J. Faller,et al. Resolution of BIPHEP on Rh with a chiral diene auxiliary , 2006 .
[18] K. Mikami,et al. Enantiodiscrimination and enantiocontrol of neutral and cationic PtII complexes bearing the tropos biphep ligand: application to asymmetric lewis acid catalysis. , 2005, Angewandte Chemie.
[19] A. Echavarren,et al. Ligand Effects in Gold- and Platinum-Catalyzed Cyclization of Enynes: Chiral Gold Complexes for Enantioselective Alkoxycyclization , 2005 .
[20] K. Mikami,et al. Racemic but tropos (chirally flexible) BIPHEP ligands for Rh(I)-complexes: highly enantioselective ene-type cyclization of 1,6-enynes. , 2004, Organic letters.
[21] Pekka Pyykkö,et al. Theoretical chemistry of gold. , 2004, Angewandte Chemie.
[22] Pekka Pyykkö. Theoretische Chemie des Golds , 2004 .
[23] K. Mikami,et al. Helical chirality control of palladium complexes that bear a tetrakis(phosphanyl)terphenyl ligand: application as asymmetric Lewis acid catalysts. , 2003, Angewandte Chemie.
[24] J. Lacour,et al. Recent developments in chiral anion mediated asymmetric chemistry. , 2003, Chemical Society reviews.
[25] Koichi Mikami,et al. Symmetry breaking in asymmetric catalysis: racemic catalysis to autocatalysis. , 2003, Chemical reviews.
[26] P. Walsh,et al. Use of achiral and meso ligands to convey asymmetry in enantioselective catalysis. , 2003, Chemical reviews.
[27] J. Parr,et al. Chiral poisoning and asymmetric activation. , 2003, Chemical reviews.
[28] K. Mikami,et al. Tropos or Atropos? That Is the Question! , 2002 .
[29] J. Sauvage,et al. Ion-pair-mediated asymmetric synthesis of a configurationally stable mononuclear tris(diimine)-iron(II) complex. , 2002, Angewandte Chemie.
[30] J. Inanaga,et al. Asymmetric catalysis and amplification with chiral lanthanide complexes. , 2002, Chemical reviews.
[31] K. Mikami,et al. Asymmetric activation of the Pd catalyst bearing the tropos biphenylphosphine (BIPHEP) ligand with the chiral diaminobinaphthyl (DABN) activator. , 2002, Organic letters.
[32] K. Mikami,et al. Resolution of Pd catalyst with tropos biphenylphosphine (BIPHEP) ligand by DM-DABN: asymmetric catalysis by an enantiopure BIPHEP-Pd complex. , 2002, Organic letters.
[33] Jennifer J. Becker,et al. Asymmetric catalysis with the normally unresolvable, conformationally dynamic 2,2'-bis(diphenylphosphino)-1,1'-biphenyl (biphep). , 2001, Journal of the American Chemical Society.
[34] S. Kawauchi,et al. Dynamic Chirality Control of (Xyl-)BIPHEP Ligands Leading to their Diastereomerically Pure Ru Complexes with a Chiral N-Substituted DPEN , 2001 .
[35] G. Balavoine,et al. The Combination of Spontaneous Resolution and Asymmetric Catalysis: A Model for the Generation of Optical Activity from a Fully Racemic System , 2001 .
[36] R. Noyori,et al. Conformationally Flexible Biphenyl-phosphane Ligands for Ru-Catalyzed Enantioselective Hydrogenation. , 1999, Angewandte Chemie.
[37] R. Noyori,et al. Konformativ flexible Biphenyl‐Phosphanliganden für Ru‐katalysierte enantioselektive Hydrierungen , 1999 .
[38] S. Bhargava,et al. Dinuclear Cycloaurated Complexes Containing Bridging (2-Diphenylphosphino)phenylphosphine and (2-Diethylphosphino)phenylphosphine, C6H4PR2(R = Ph, Et). Carbon−Carbon Bond Formation by Reductive Elimination at a Gold(II)−Gold(II) Center , 1996 .
[39] Furuno,et al. Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system , 2000, Organic letters.
[40] E. Jacobsen,et al. Comprehensive Asymmetric Catalysis I–III , 1999 .
[41] M. Schlosser,et al. The activation barrier to axial torsion in 2,2'-bis(diphenylphosphino)biphenyl , 1996 .
[42] G. Yamamoto,et al. Effects of para -Substituents on the Rates of Inversion of Biphenyl Derivatives. II. 2-Isopropyl-2′-methoxybiphenyls , 1971 .