Topics in Current Chemistry (2019) 377:31
1 3
50. Mechler M, Peters R (2015) Diastereodivergent asymmetric 1,4-addition of oxindoles to nitroolefins by using polyfunctional nickel-hydrogen-bond-azolium catalysts. Angew Chem Int Ed
54:10303–10307
51. Krautwald S, Sarlah D, Schafroth MA, Carreira EM (2013) Enantio- and diastereodivergent dual
catalysis: α-allylation of branched aldehydes. Science 340:1065–1068
52. Sandmeier T, Krautwald S, Zipfel HF, Carreira EM (2015) Stereodivergent dual catalytic α-allylation
of protected α-amino- and α-hydroxyacetaldehydes. Angew Chem Int Ed 54:14363–14367
53. Schmid J, Junge T, Lang J, Frey W, Peters R (2019) Polyfunctional bis-Lewis-acid-/bis-triazolium catalysts for stereoselective 1,4-additions of 2-oxindoles to maleimides. Angew Chem Int Ed
58:5447–5451
54. Satyanarayana T, Abraham S, Kagan HB (2009) Nonlinear effects in asymmetric catalysis. Angew
Chem Int Ed 48:456–494
55. Ohmatsu K, Imagawa N, Ooi T (2014) Ligand-enabled multiple absolute stereocontrol in metal-catalysed cycloaddition for construction of contiguous all-carbon quaternary stereocentres. Nat Chem
6:47–51
56. Schärer K, Morgenthaler M, Seiler P, Diederich F (2004) Enantiomerically pure thrombin inhibitors for exploring the molecular-recognition features of the oxyanion hole. Helv Chim Acta
87:2517–2538
57. Ohmatsu K, Kawai S, Imagawa N, Ooi T (2014) Palladium-catalyzed asymmetric [3 + 2] cycloaddition of 5-vinyloxazolidinones with imines using chiral ammonium- phosphine hybrid ligand. ACS
Catal 4:4304–4306
58. Reetz MT (2009) Directed evolution of enantioselective enzymes: an unconventional approach to
asymmetric catalysis in organic chemistry. J Org Chem 74:5767–5778
59. Reetz MT (2011) Laboratory evolution of stereoselective enzymes: a prolific source of catalysts for
asymmetric reactions. Angew Chem Int Ed 50:138–174
60. Müller M (2012) Recent developments in enzymatic asymmetric C-C bond formation. Adv Synth
Catal 354:3161–3174
61. Breit B (2008) Catalysts through self-assembly for combinatorial homogeneous catalysis. Pure Appl
Chem 80:855–860
62. Meeuwissen J, Reek JNH (2010) Supramolecular catalysis beyond enzyme mimics. Nat Chem
2:615–621
63. Ohmatsu K, Ooi T (2015) Design of supramolecular chiral ligands for asymmetric metal catalysis.
Tetrahedron Lett 56:2043–2048
64. Ohmatsu K, Ito M, Kunieda T, Ooi Takashi (2012) Ion-paired chiral ligands for asymmetric palladium catalysis. Nat Chem 4:473–477
65. Akiyama T (2007) Stronger Brønsted acids. Chem Rev 107:5744–5758
66. Terada M (2010) Chiral phosphoric acids as versatile catalysts for enantioselective transformations.
Synthesis 2010:1929–1982
67. Phipps RJ, Hamilton GL, Toste FD (2012) The progression of chiral anions from concepts to applications in asymmetric catalysis. Nat Chem 4:603–614
68. Mahlau M, List B (2012) Asymmetric counteranion-directed catalysis: concept, definition, and
applications. Angew Chem Int Ed 52:518–533
69. Brak K, Jacobsen EN (2013) Asymmetric ion-pairing catalysis. Angew Chem Int Ed 52:534–561
70. Ohmatsu K, Ito M, Ooi T (2014) Ligand-controlled E/Z selectivity and enantioselectivity in palladium-catalyzed allylation of benzofuranones with 1,2-disubstituted allylic carbonates. Chem Commun 50:4554–4557
71. Ohmatsu K, Ito M, Kunieda T, Ooi T (2013) Exploiting the modularity of ion-paired chiral ligands
for palladium-catalyzed enantioselective allylation of benzofuran-2(3H)-ones. J Am Chem Soc
135:590–593
72. Wieland J, Breit B (2010) A combinatorial approach to the identification of self-assembled ligands
for rhodium-catalysed asymmetric hydrogenation. Nat Chem 2:832–837
73. Ohmatsu K, Hara Y, Ooi T (2014) In situ generation of ion-paired chiral ligands: rapid identification
of the optimal ligand for palladium-catalyzed asymmetric allylation. Chem Sci 5:3645–3650
Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published
maps and institutional affiliations.
Reprinted from the journal
152
1 3
50. Mechler M, Peters R (2015) Diastereodivergent asymmetric 1,4-addition of oxindoles to nitroolefins by using polyfunctional nickel-hydrogen-bond-azolium catalysts. Angew Chem Int Ed
54:10303–10307
51. Krautwald S, Sarlah D, Schafroth MA, Carreira EM (2013) Enantio- and diastereodivergent dual
catalysis: α-allylation of branched aldehydes. Science 340:1065–1068
52. Sandmeier T, Krautwald S, Zipfel HF, Carreira EM (2015) Stereodivergent dual catalytic α-allylation
of protected α-amino- and α-hydroxyacetaldehydes. Angew Chem Int Ed 54:14363–14367
53. Schmid J, Junge T, Lang J, Frey W, Peters R (2019) Polyfunctional bis-Lewis-acid-/bis-triazolium catalysts for stereoselective 1,4-additions of 2-oxindoles to maleimides. Angew Chem Int Ed
58:5447–5451
54. Satyanarayana T, Abraham S, Kagan HB (2009) Nonlinear effects in asymmetric catalysis. Angew
Chem Int Ed 48:456–494
55. Ohmatsu K, Imagawa N, Ooi T (2014) Ligand-enabled multiple absolute stereocontrol in metal-catalysed cycloaddition for construction of contiguous all-carbon quaternary stereocentres. Nat Chem
6:47–51
56. Schärer K, Morgenthaler M, Seiler P, Diederich F (2004) Enantiomerically pure thrombin inhibitors for exploring the molecular-recognition features of the oxyanion hole. Helv Chim Acta
87:2517–2538
57. Ohmatsu K, Kawai S, Imagawa N, Ooi T (2014) Palladium-catalyzed asymmetric [3 + 2] cycloaddition of 5-vinyloxazolidinones with imines using chiral ammonium- phosphine hybrid ligand. ACS
Catal 4:4304–4306
58. Reetz MT (2009) Directed evolution of enantioselective enzymes: an unconventional approach to
asymmetric catalysis in organic chemistry. J Org Chem 74:5767–5778
59. Reetz MT (2011) Laboratory evolution of stereoselective enzymes: a prolific source of catalysts for
asymmetric reactions. Angew Chem Int Ed 50:138–174
60. Müller M (2012) Recent developments in enzymatic asymmetric C-C bond formation. Adv Synth
Catal 354:3161–3174
61. Breit B (2008) Catalysts through self-assembly for combinatorial homogeneous catalysis. Pure Appl
Chem 80:855–860
62. Meeuwissen J, Reek JNH (2010) Supramolecular catalysis beyond enzyme mimics. Nat Chem
2:615–621
63. Ohmatsu K, Ooi T (2015) Design of supramolecular chiral ligands for asymmetric metal catalysis.
Tetrahedron Lett 56:2043–2048
64. Ohmatsu K, Ito M, Kunieda T, Ooi Takashi (2012) Ion-paired chiral ligands for asymmetric palladium catalysis. Nat Chem 4:473–477
65. Akiyama T (2007) Stronger Brønsted acids. Chem Rev 107:5744–5758
66. Terada M (2010) Chiral phosphoric acids as versatile catalysts for enantioselective transformations.
Synthesis 2010:1929–1982
67. Phipps RJ, Hamilton GL, Toste FD (2012) The progression of chiral anions from concepts to applications in asymmetric catalysis. Nat Chem 4:603–614
68. Mahlau M, List B (2012) Asymmetric counteranion-directed catalysis: concept, definition, and
applications. Angew Chem Int Ed 52:518–533
69. Brak K, Jacobsen EN (2013) Asymmetric ion-pairing catalysis. Angew Chem Int Ed 52:534–561
70. Ohmatsu K, Ito M, Ooi T (2014) Ligand-controlled E/Z selectivity and enantioselectivity in palladium-catalyzed allylation of benzofuranones with 1,2-disubstituted allylic carbonates. Chem Commun 50:4554–4557
71. Ohmatsu K, Ito M, Kunieda T, Ooi T (2013) Exploiting the modularity of ion-paired chiral ligands
for palladium-catalyzed enantioselective allylation of benzofuran-2(3H)-ones. J Am Chem Soc
135:590–593
72. Wieland J, Breit B (2010) A combinatorial approach to the identification of self-assembled ligands
for rhodium-catalysed asymmetric hydrogenation. Nat Chem 2:832–837
73. Ohmatsu K, Hara Y, Ooi T (2014) In situ generation of ion-paired chiral ligands: rapid identification
of the optimal ligand for palladium-catalyzed asymmetric allylation. Chem Sci 5:3645–3650
Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published
maps and institutional affiliations.
Reprinted from the journal
152