메뉴 건너뛰기




Volumn 46, Issue 4, 2013, Pages 885-893

The cation-π interaction

Author keywords

[No Author keywords available]

Indexed keywords

ANION; BENZENE; CARBON; CATION; HYDROGEN; PHENYLALANINE; PROTEIN; TRYPTOPHAN; WATER;

EID: 84876275836     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar300265y     Document Type: Article
Times cited : (936)

References (62)
  • 1
    • 0038100343 scopus 로고
    • Ion-solvent molecule interactions in the gas phase. The potassium ion and benzene
    • Sunner, J.; Nishizawa, K.; Kebarle, P. Ion-solvent molecule interactions in the gas phase. The potassium ion and benzene J. Phys. Chem. 1981, 85, 1814-1820
    • (1981) J. Phys. Chem. , vol.85 , pp. 1814-1820
    • Sunner, J.1    Nishizawa, K.2    Kebarle, P.3
  • 2
    • 0000733668 scopus 로고    scopus 로고
    • + by benzene and water: Cation-pi interactions and pi-hydrogen bonds
    • + by benzene and water: Cation-pi interactions and pi-hydrogen bonds J. Chem. Phys. 1998, 108, 5151-5154
    • (1998) J. Chem. Phys. , vol.108 , pp. 5151-5154
    • Cabarcos, O.M.1    Weinheimer, C.J.2    Lisy, J.M.3
  • 4
    • 4243468938 scopus 로고    scopus 로고
    • The cation-π interaction
    • Ma, J. C.; Dougherty, D. A. The cation-π interaction Chem. Rev. 1997, 97, 1303-1324
    • (1997) Chem. Rev. , vol.97 , pp. 1303-1324
    • Ma, J.C.1    Dougherty, D.A.2
  • 5
    • 0034499001 scopus 로고    scopus 로고
    • Absolute binding energies of alkali-metal cation complexes with benzene determined by threshold collision-induced dissociation experiments and ab initio theory
    • Amicangelo, J. C.; Armentrout, P. B. Absolute binding energies of alkali-metal cation complexes with benzene determined by threshold collision-induced dissociation experiments and ab initio theory J. Phys. Chem. A 2000, 104, 11420-11432
    • (2000) J. Phys. Chem. A , vol.104 , pp. 11420-11432
    • Amicangelo, J.C.1    Armentrout, P.B.2
  • 6
    • 0037468201 scopus 로고    scopus 로고
    • Cation-π interactions: A theoretical investigation of the interaction of metallic and organic cations with alkenes, arenes, and heteroarenes
    • Kim, D.; Hu, S.; Tarakeshwar, P.; Kim, K. S. Cation-π interactions: A theoretical investigation of the interaction of metallic and organic cations with alkenes, arenes, and heteroarenes J. Phys. Chem. A 2003, 107, 1228-1238
    • (2003) J. Phys. Chem. A , vol.107 , pp. 1228-1238
    • Kim, D.1    Hu, S.2    Tarakeshwar, P.3    Kim, K.S.4
  • 7
    • 33845377147 scopus 로고
    • +⋯π. Complexes of onium ions with olefins and benzene derivatives
    • +⋯π. Complexes of onium ions with olefins and benzene derivatives J. Am. Chem. Soc. 1985, 107, 474-479
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 474-479
    • Deakyne, C.A.1    Meot-Ner, M.2
  • 8
    • 33845376733 scopus 로고
    • δ+⋯X. Complexes of quaternary ions with n- and π-Donors
    • δ+⋯X. Complexes of quaternary ions with n- and π-Donors J. Am. Chem. Soc. 1985, 107, 469-474
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 469-474
    • Meot-Ner, M.1    Deakyne, C.A.2
  • 9
    • 0010712815 scopus 로고
    • Design and synthesis of a new class of hydrophobic binding sites
    • Petti, M. A.; Shepodd, T. J.; Dougherty, D. A. Design and synthesis of a new class of hydrophobic binding sites Tetrahedron Lett. 1986, 27, 807-810
    • (1986) Tetrahedron Lett. , vol.27 , pp. 807-810
    • Petti, M.A.1    Shepodd, T.J.2    Dougherty, D.A.3
  • 10
    • 0000656247 scopus 로고
    • A new water-soluble macrocyclic host of the cyclophane type: Host-guest complexation with aromatic guests in aqueous solution and acceleration of the transport of arenes through an aqueous phase
    • Diederich, F.; Dick, K. A new water-soluble macrocyclic host of the cyclophane type: Host-guest complexation with aromatic guests in aqueous solution and acceleration of the transport of arenes through an aqueous phase J. Am. Chem. Soc. 1984, 106, 8024-8036
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 8024-8036
    • Diederich, F.1    Dick, K.2
  • 11
    • 0025343507 scopus 로고
    • Strength of molecular complexation of apolar solutes in water and in organic solvents is predictable by linear free energy relationships: A general model for solvation effects on apolar binding
    • Smithrud, D. B.; Diederich, F. Strength of molecular complexation of apolar solutes in water and in organic solvents is predictable by linear free energy relationships: A general model for solvation effects on apolar binding J. Am. Chem. Soc. 1990, 112, 339-343
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 339-343
    • Smithrud, D.B.1    Diederich, F.2
  • 12
    • 0005633213 scopus 로고
    • Tight, oriented binding of an aliphatic guest by a new class of water-soluble molecules with hydrophobic bindings sites
    • Shepodd, T. J.; Petti, M. A.; Dougherty, D. A. Tight, oriented binding of an aliphatic guest by a new class of water-soluble molecules with hydrophobic bindings sites J. Am. Chem. Soc. 1986, 108, 6085-6087
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6085-6087
    • Shepodd, T.J.1    Petti, M.A.2    Dougherty, D.A.3
  • 13
    • 0022450133 scopus 로고
    • Amino-aromatic interactions in proteins
    • Burley, S. K.; Petsko, G. A. Amino-aromatic interactions in proteins FEBS Lett. 1986, 203, 139-143
    • (1986) FEBS Lett. , vol.203 , pp. 139-143
    • Burley, S.K.1    Petsko, G.A.2
  • 14
    • 2142775205 scopus 로고
    • Molecular recognition in aqueous media: Donor-acceptor and ion-dipole interactions produce tight binding for highly soluble guests
    • Shepodd, T. J.; Petti, M. A.; Dougherty, D. A. Molecular recognition in aqueous media: Donor-acceptor and ion-dipole interactions produce tight binding for highly soluble guests J. Am. Chem. Soc. 1988, 110, 1983-1985
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1983-1985
    • Shepodd, T.J.1    Petti, M.A.2    Dougherty, D.A.3
  • 15
    • 0022634647 scopus 로고
    • Hemoglobin as a receptor of drugs and peptides: X-ray studies of the stereochemistry of binding
    • Perutz, M. F.; Fermi, G.; Abraham, D. J.; Poyart, C.; Bursaux, E. Hemoglobin as a receptor of drugs and peptides: X-ray studies of the stereochemistry of binding J. Am. Chem. Soc. 1986, 108, 1064-1078
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 1064-1078
    • Perutz, M.F.1    Fermi, G.2    Abraham, D.J.3    Poyart, C.4    Bursaux, E.5
  • 16
    • 0024292833 scopus 로고
    • Aromatic rings act as hydrogen bond acceptors
    • Levitt, M.; Perutz, M. F. Aromatic rings act as hydrogen bond acceptors J. Mol. Biol. 1988, 201, 751-754
    • (1988) J. Mol. Biol. , vol.201 , pp. 751-754
    • Levitt, M.1    Perutz, M.F.2
  • 17
    • 0028301445 scopus 로고
    • Amino/aromatic interactions in proteins: Is the evidence stacked against hydrogen bonding?
    • Mitchell, J. B. O.; Nandi, C. L.; McDonald, I. K.; Thornton, J. M.; Price, S. L. Amino/aromatic interactions in proteins: Is the evidence stacked against hydrogen bonding? J. Mol. Biol. 1994, 239, 315-331
    • (1994) J. Mol. Biol. , vol.239 , pp. 315-331
    • Mitchell, J.B.O.1    Nandi, C.L.2    McDonald, I.K.3    Thornton, J.M.4    Price, S.L.5
  • 18
    • 33845278120 scopus 로고
    • "hydrophobic" binding of water-soluble guests by high-symmetry, chiral hosts. An electron-rich receptor site with a general affinity for quaternary ammonium compounds and electron-deficient π systems
    • Petti, M. A.; Shepodd, T. J.; Barrans, R. E., Jr.; Dougherty, D. A. "Hydrophobic" binding of water-soluble guests by high-symmetry, chiral hosts. An electron-rich receptor site with a general affinity for quaternary ammonium compounds and electron-deficient π systems J. Am. Chem. Soc. 1988, 110, 6825-6840
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 6825-6840
    • Petti, M.A.1    Shepodd, T.J.2    Barrans Jr., R.E.3    Dougherty, D.A.4
  • 19
    • 12044260020 scopus 로고
    • Molecular recognition in aqueous media. New binding studies provide further insights into the cation-π interaction and related phenomena
    • Kearney, P. C.; Mizoue, L. S.; Kumpf, R. A.; Forman, J. E.; McCurdy, A.; Dougherty, D. A. Molecular recognition in aqueous media. New binding studies provide further insights into the cation-π interaction and related phenomena J. Am. Chem. Soc. 1993, 115, 9907-9919
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9907-9919
    • Kearney, P.C.1    Mizoue, L.S.2    Kumpf, R.A.3    Forman, J.E.4    McCurdy, A.5    Dougherty, D.A.6
  • 22
    • 33751552981 scopus 로고
    • Concerning the thermodynamics of molecular recognition in aqueous and organic media. Evidence for significant heat capacity effects
    • Stauffer, D. A.; Barrans, R. E., Jr.; Dougherty, D. A. Concerning the thermodynamics of molecular recognition in aqueous and organic media. Evidence for significant heat capacity effects J. Org. Chem. 1990, 55, 2762-2767
    • (1990) J. Org. Chem. , vol.55 , pp. 2762-2767
    • Stauffer, D.A.1    Barrans Jr., R.E.2    Dougherty, D.A.3
  • 23
    • 0025675821 scopus 로고
    • Acetylcholine binding by a synthetic receptor. Implications for biological recognition
    • Dougherty, D. A.; Stauffer, D. A. Acetylcholine binding by a synthetic receptor. Implications for biological recognition Science 1990, 250, 1558-1560
    • (1990) Science , vol.250 , pp. 1558-1560
    • Dougherty, D.A.1    Stauffer, D.A.2
  • 24
    • 0025778840 scopus 로고
    • Atomic structure of acetylcholinesterase from Torpedo californica: A prototypic acetylcholine-binding protein
    • Sussman, J. L.; Harel, M.; Frolow, F.; Oefner, C.; Goldman, A.; Toker, L.; Silman, I. Atomic structure of acetylcholinesterase from Torpedo californica: A prototypic acetylcholine-binding protein Science 1991, 253, 872-879
    • (1991) Science , vol.253 , pp. 872-879
    • Sussman, J.L.1    Harel, M.2    Frolow, F.3    Oefner, C.4    Goldman, A.5    Toker, L.6    Silman, I.7
  • 26
    • 16344389701 scopus 로고    scopus 로고
    • Cation-π interactions in protein-protein interfaces
    • Crowley, P. B.; Golovin, A. Cation-π interactions in protein-protein interfaces Proteins 2005, 59, 231-239
    • (2005) Proteins , vol.59 , pp. 231-239
    • Crowley, P.B.1    Golovin, A.2
  • 27
    • 0001227655 scopus 로고
    • The nature of π-π Interactions
    • Hunter, C. A.; Sanders, J. K. M. The nature of π-π interactions J. Am. Chem. Soc. 1990, 112, 5525-5534
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5525-5534
    • Hunter, C.A.1    Sanders, J.K.M.2
  • 28
    • 0029967521 scopus 로고    scopus 로고
    • Cation-π interactions in simple aromatics. Electrostatics provide a predictive tool
    • Mecozzi, S.; West, A. P., Jr.; Dougherty, D. A. Cation-π interactions in simple aromatics. Electrostatics provide a predictive tool J. Am. Chem. Soc. 1996, 118, 2307-2308
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2307-2308
    • Mecozzi, S.1    West Jr., A.P.2    Dougherty, D.A.3
  • 29
    • 0029745052 scopus 로고    scopus 로고
    • Cation-π interactions in aromatics of biological and medicinal interest: Electrostatic potential surfaces as a useful qualitative guide
    • Mecozzi, S.; West, A. P., Jr.; Dougherty, D. A. Cation-π interactions in aromatics of biological and medicinal interest: Electrostatic potential surfaces as a useful qualitative guide Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 10566-10571
    • (1996) Proc. Natl. Acad. Sci. U.S.A. , vol.93 , pp. 10566-10571
    • Mecozzi, S.1    West Jr., A.P.2    Dougherty, D.A.3
  • 30
    • 67749097785 scopus 로고    scopus 로고
    • Substituent effects in cation-π interactions and electrostatic potentials above the centers of substituted benzenes are due primarily to through-space effects of the substituents
    • Wheeler, S. E.; Houk, K. N. Substituent effects in cation-π interactions and electrostatic potentials above the centers of substituted benzenes are due primarily to through-space effects of the substituents J. Am. Chem. Soc. 2009, 131, 3126-3127
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3126-3127
    • Wheeler, S.E.1    Houk, K.N.2
  • 31
    • 0030043489 scopus 로고    scopus 로고
    • Cation-π interactions in chemistry and biology. A new view of benzene, Phe, Tyr, and Trp
    • Dougherty, D. A. Cation-π interactions in chemistry and biology. A new view of benzene, Phe, Tyr, and Trp Science 1996, 271, 163-168
    • (1996) Science , vol.271 , pp. 163-168
    • Dougherty, D.A.1
  • 32
    • 0242417008 scopus 로고    scopus 로고
    • Interactions with aromatic rings in chemical and biological recognition
    • Meyer, E. A.; Castellano, R. K.; Diederich, F. Interactions with aromatic rings in chemical and biological recognition Angew. Chem., Int. Ed. 2003, 42, 1210-1250
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 1210-1250
    • Meyer, E.A.1    Castellano, R.K.2    Diederich, F.3
  • 33
    • 79955766939 scopus 로고    scopus 로고
    • Aromatic rings in chemical and biological recognition: Energetics and structures
    • Salonen, L. M.; Ellermann, M.; Diederich, F. Aromatic rings in chemical and biological recognition: Energetics and structures Angew. Chem., Int. Ed. 2011, 50, 4808-4842
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4808-4842
    • Salonen, L.M.1    Ellermann, M.2    Diederich, F.3
  • 34
    • 70349782154 scopus 로고    scopus 로고
    • Binding mechanisms in supramolecular complexes
    • Schneider, H.-J. Binding mechanisms in supramolecular complexes Angew. Chem., Int. Ed. 2009, 48, 3924-3977
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 3924-3977
    • Schneider, H.-J.1
  • 35
    • 22744448212 scopus 로고    scopus 로고
    • Quantification of cation-pi interactions in protein-ligand complexes: Crystal-structure analysis of factor Xa bound to a quaternary ammonium ion ligand
    • Scharer, K.; Morgenthaler, M.; Paulini, R.; Obst-Sander, U.; Banner, D. W.; Schlatter, D.; Benz, J.; Stihle, M.; Diederich, F. Quantification of cation-pi interactions in protein-ligand complexes: Crystal-structure analysis of factor Xa bound to a quaternary ammonium ion ligand Angew. Chem., Int. Ed. 2005, 44, 4400-4404
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 4400-4404
    • Scharer, K.1    Morgenthaler, M.2    Paulini, R.3    Obst-Sander, U.4    Banner, D.W.5    Schlatter, D.6    Benz, J.7    Stihle, M.8    Diederich, F.9
  • 36
    • 0032558123 scopus 로고    scopus 로고
    • Energetic analysis of an engineered cation-π interaction in staphylococcal nuclease
    • Ting, A. Y.; Shin, I.; Lucero, C.; Schultz, P. G. Energetic analysis of an engineered cation-π interaction in staphylococcal nuclease J. Am. Chem. Soc. 1998, 120, 7135-7136
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 7135-7136
    • Ting, A.Y.1    Shin, I.2    Lucero, C.3    Schultz, P.G.4
  • 40
    • 0032514762 scopus 로고    scopus 로고
    • From ab initio quantum mechanics to molecular neurobiology: A cation-π binding site in the nicotinic receptor
    • Zhong, W.; Gallivan, J. P.; Zhang, Y.; Li, L.; Lester, H. A.; Dougherty, D. A. From ab initio quantum mechanics to molecular neurobiology: A cation-π binding site in the nicotinic receptor Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 12088-12093
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 12088-12093
    • Zhong, W.1    Gallivan, J.P.2    Zhang, Y.3    Li, L.4    Lester, H.A.5    Dougherty, D.A.6
  • 41
    • 44849128243 scopus 로고    scopus 로고
    • Cys-loop neuroreceptors: Structure to the rescue?
    • Dougherty, D. A. Cys-loop neuroreceptors: Structure to the rescue? Chem. Rev. 2008, 108, 1642-1653
    • (2008) Chem. Rev. , vol.108 , pp. 1642-1653
    • Dougherty, D.A.1
  • 42
    • 79957953215 scopus 로고    scopus 로고
    • Principles of activation and permeation in an anion-selective Cys-loop receptor
    • Hibbs, R. E.; Gouaux, E. Principles of activation and permeation in an anion-selective Cys-loop receptor Nature 2011, 474, 54-60
    • (2011) Nature , vol.474 , pp. 54-60
    • Hibbs, R.E.1    Gouaux, E.2
  • 43
    • 63649149427 scopus 로고    scopus 로고
    • Nicotine binding to brain receptors requires a strong cation-π interaction
    • Xiu, X.; Puskar, N. L.; Shanata, J. A. P.; Lester, H. A.; Dougherty, D. A. Nicotine binding to brain receptors requires a strong cation-π interaction Nature 2009, 458, 534-537
    • (2009) Nature , vol.458 , pp. 534-537
    • Xiu, X.1    Puskar, N.L.2    Shanata, J.A.P.3    Lester, H.A.4    Dougherty, D.A.5
  • 44
    • 0029087136 scopus 로고
    • Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity
    • Sine, S. M.; Ohno, K.; Bouzat, C.; Auerbach, A.; Milone, M.; Pruitt, J. N.; Engel, A. G. Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity Neuron 1995, 15, 229-239
    • (1995) Neuron , vol.15 , pp. 229-239
    • Sine, S.M.1    Ohno, K.2    Bouzat, C.3    Auerbach, A.4    Milone, M.5    Pruitt, J.N.6    Engel, A.G.7
  • 45
    • 70450177454 scopus 로고    scopus 로고
    • +-π interactions in the catalytic site of T1 lipase revealed by molecular dynamics simulations
    • +-π interactions in the catalytic site of T1 lipase revealed by molecular dynamics simulations J. Am. Chem. Soc. 2009, 131, 16697-16705
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 16697-16705
    • Hagiwara, Y.1    Matsumura, H.2    Tateno, M.3
  • 46
    • 34848876603 scopus 로고    scopus 로고
    • Calcium block of single sodium channels: Role of a pore-lining aromatic residue
    • Santarelli, V. P.; Eastwood, A. L.; Dougherty, D. A.; Ahern, C. A.; Horn, R. Calcium block of single sodium channels: Role of a pore-lining aromatic residue Biophys. J. 2007, 93, 2341-2349
    • (2007) Biophys. J. , vol.93 , pp. 2341-2349
    • Santarelli, V.P.1    Eastwood, A.L.2    Dougherty, D.A.3    Ahern, C.A.4    Horn, R.5
  • 48
    • 72449163457 scopus 로고    scopus 로고
    • RNA-amino acid binding: A stereochemical era for the genetic code
    • Yarus, M.; Widmann, J. J.; Knight, R. RNA-amino acid binding: A stereochemical era for the genetic code J. Mol. Evol. 2009, 69, 406-429
    • (2009) J. Mol. Evol. , vol.69 , pp. 406-429
    • Yarus, M.1    Widmann, J.J.2    Knight, R.3
  • 49
    • 0036796820 scopus 로고    scopus 로고
    • Lariat ether receptor systems show experimental evidence for alkali metal cation-π interactions
    • Gokel, G. W.; Barbour, L. J.; Ferdani, R.; Hu, J. Lariat ether receptor systems show experimental evidence for alkali metal cation-π interactions Acc. Chem. Res. 2002, 35, 878-886
    • (2002) Acc. Chem. Res. , vol.35 , pp. 878-886
    • Gokel, G.W.1    Barbour, L.J.2    Ferdani, R.3    Hu, J.4
  • 50
    • 0035902009 scopus 로고    scopus 로고
    • Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors
    • Brejc, K.; van Dijk, W. J.; Klaassen, R. V.; Schuurmans, M.; van Der Oost, J.; Smit, A. B.; Sixma, T. K. Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors Nature 2001, 411, 269-276
    • (2001) Nature , vol.411 , pp. 269-276
    • Brejc, K.1    Van Dijk, W.J.2    Klaassen, R.V.3    Schuurmans, M.4    Van Der Oost, J.5    Smit, A.B.6    Sixma, T.K.7
  • 52
    • 0029828395 scopus 로고    scopus 로고
    • Cation-pi bonding and amino-aromatic interactions in the biomolecular recognition of substituted ammonium ligands
    • Scrutton, N. S.; Raine, A. R. Cation-pi bonding and amino-aromatic interactions in the biomolecular recognition of substituted ammonium ligands Biochem. J. 1996, 319 (Pt 1) 1-8
    • (1996) Biochem. J. , vol.319 , Issue.PART 1 , pp. 1-8
    • Scrutton, N.S.1    Raine, A.R.2
  • 53
    • 35848961668 scopus 로고    scopus 로고
    • How chromatin-binding modules interpret histone modifications: Lessons from professional pocket pickers
    • Taverna, S. D.; Li, H.; Ruthenburg, A. J.; Allis, C. D.; Patel, D. J. How chromatin-binding modules interpret histone modifications: Lessons from professional pocket pickers Nat. Struct. Mol. Biol. 2007, 14, 1025-1040
    • (2007) Nat. Struct. Mol. Biol. , vol.14 , pp. 1025-1040
    • Taverna, S.D.1    Li, H.2    Ruthenburg, A.J.3    Allis, C.D.4    Patel, D.J.5
  • 54
    • 34547427285 scopus 로고    scopus 로고
    • Recognition of trimethyllysine by a chromodomain is not driven by the hydrophobic effect
    • Hughes, R. M.; Wiggins, K. R.; Khorasanizadeh, S.; Waters, M. L. Recognition of trimethyllysine by a chromodomain is not driven by the hydrophobic effect Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 11184-11188
    • (2007) Proc. Natl. Acad. Sci. U.S.A. , vol.104 , pp. 11184-11188
    • Hughes, R.M.1    Wiggins, K.R.2    Khorasanizadeh, S.3    Waters, M.L.4
  • 55
    • 0347065346 scopus 로고    scopus 로고
    • Insertion of an N7-methylguanine mRNA cap between two coplanar aromatic residues of a cap-binding protein is fast and selective for a positively charged cap
    • Hu, G.; Tsai, A. L.; Quiocho, F. A. Insertion of an N7-methylguanine mRNA cap between two coplanar aromatic residues of a cap-binding protein is fast and selective for a positively charged cap J. Biol. Chem. 2003, 278, 51515-51520
    • (2003) J. Biol. Chem. , vol.278 , pp. 51515-51520
    • Hu, G.1    Tsai, A.L.2    Quiocho, F.A.3
  • 56
  • 57
    • 36349025257 scopus 로고    scopus 로고
    • Enzymatic synthesis of cyclic triterpenes
    • Abe, I. Enzymatic synthesis of cyclic triterpenes Nat. Prod. Rep. 2007, 24, 1311-1331
    • (2007) Nat. Prod. Rep. , vol.24 , pp. 1311-1331
    • Abe, I.1
  • 58
    • 33749529751 scopus 로고    scopus 로고
    • Cation-π interaction in the polyolefin cyclization cascade uncovered by incorporating unnatural amino acids into the catalytic sites of squalene cyclase
    • Morikubo, N.; Fukuda, Y.; Ohtake, K.; Shinya, N.; Kiga, D.; Sakamoto, K.; Asanuma, M.; Hirota, H.; Yokoyama, S.; Hoshino, T. Cation-π interaction in the polyolefin cyclization cascade uncovered by incorporating unnatural amino acids into the catalytic sites of squalene cyclase J. Am. Chem. Soc. 2006, 128, 13184-13194
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 13184-13194
    • Morikubo, N.1    Fukuda, Y.2    Ohtake, K.3    Shinya, N.4    Kiga, D.5    Sakamoto, K.6    Asanuma, M.7    Hirota, H.8    Yokoyama, S.9    Hoshino, T.10
  • 61
    • 77950805314 scopus 로고    scopus 로고
    • Enantioselective thiourea-catalyzed cationic polycyclizations
    • Knowles, R. R.; Lin, S.; Jacobsen, E. N. Enantioselective thiourea-catalyzed cationic polycyclizations J. Am. Chem. Soc. 2010, 132, 5030-5032
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 5030-5032
    • Knowles, R.R.1    Lin, S.2    Jacobsen, E.N.3
  • 62
    • 79953879649 scopus 로고    scopus 로고
    • Transition-state charge stabilization through multiple non-covalent interactions in the guanidinium-catalyzed enantioselective claisen rearrangement
    • Uyeda, C.; Jacobsen, E. N. Transition-state charge stabilization through multiple non-covalent interactions in the guanidinium-catalyzed enantioselective claisen rearrangement J. Am. Chem. Soc. 2011, 133, 5062-5075
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 5062-5075
    • Uyeda, C.1    Jacobsen, E.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.