-
1
-
-
77953631827
-
A medicinal chemist's guide to molecular interactions
-
Bissantz C, Kuhn B, Stahl M (2010) A medicinal chemist's guide to molecular interactions. J Med Chem 53:5061-5084.
-
(2010)
J Med Chem
, vol.53
, pp. 5061-5084
-
-
Bissantz, C.1
Kuhn, B.2
Stahl, M.3
-
4
-
-
70349782154
-
Binding mechanisms in supramolecular catalysis
-
Schneider HJ (2009) Binding mechanisms in supramolecular catalysis. Angew Chem Int Ed 48:3924-3977.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 3924-3977
-
-
Schneider, H.J.1
-
7
-
-
0035384248
-
Frommolecules tocrystal engineering: Supramolecular isomerism and polymorphismin network solids
-
MoultonB, ZaworotkoMJ (2001) Frommolecules tocrystal engineering: Supramolecular isomerism and polymorphismin network solids. Chem Rev 101:1629-1658.
-
(2001)
Chem Rev
, vol.101
, pp. 1629-1658
-
-
Moulton, B.1
Zaworotko, M.J.2
-
8
-
-
0042903226
-
The hydrogen bond and crystal engineering
-
Aakeroy CB, Seddon KR (1993) The hydrogen bond and crystal engineering. Chem Soc Rev 22:397-407.
-
(1993)
Chem Soc Rev
, vol.22
, pp. 397-407
-
-
Aakeroy, C.B.1
Seddon, K.R.2
-
11
-
-
0242417008
-
Interactions with aromatic rings in chemical biological recognition
-
Meyer EA, Castellano RK, Diederich F (2003) Interactions with aromatic rings in chemical biological recognition. Angew Chem Int Ed Engl 42:1210-1250.
-
(2003)
Angew Chem Int Ed Engl
, vol.42
, pp. 1210-1250
-
-
Meyer, E.A.1
Castellano, R.K.2
Diederich, F.3
-
12
-
-
4243468938
-
The cation-p interaction
-
Ma JC, Dougherty DA (1997) The cation-p interaction. Chem Rev 97:1303-1324.
-
(1997)
Chem Rev
, vol.97
, pp. 1303-1324
-
-
Ma, J.C.1
Dougherty, D.A.2
-
15
-
-
33947547892
-
Molecular architecture and biological reactions
-
Pauling L (1946) Molecular architecture and biological reactions. Chem Eng News 24:1377.
-
(1946)
Chem Eng News
, vol.24
, pp. 1377
-
-
Pauling, L.1
-
17
-
-
33748633480
-
Electrostatic basis for enzyme catalysis
-
Warshel A, et al. (2006) Electrostatic basis for enzyme catalysis. Chem Rev 106:3210-3235.
-
(2006)
Chem Rev
, vol.106
, pp. 3210-3235
-
-
Warshel, A.1
-
18
-
-
33750620556
-
Predicting the stereochemistry of diphenylphosphino benzoic acid (DPPBA)-based palladium-catalyzed asymmetric allylic alkylation reactions: A working model
-
Trost BM, Machacek MR, Aponick A (2006) Predicting the stereochemistry of diphenylphosphino benzoic acid (DPPBA)-based palladium-catalyzed asymmetric allylic alkylation reactions: a working model. Acc Chem Res 39:747-760.
-
(2006)
Acc Chem Res
, vol.39
, pp. 747-760
-
-
Trost, B.M.1
MacHacek, M.R.2
Aponick, A.3
-
19
-
-
0037138701
-
Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis
-
Austin JF, MacMillan DW (2002) Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis. J Am Chem Soc 124:1172-1173.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 1172-1173
-
-
Austin, J.F.1
MacMillan, D.W.2
-
20
-
-
0026452321
-
Highly enantioselective catalytic Diels-Alder addition promoted by a chiral bis (oxazoline)-magnesium complex
-
Corey EJ, Ishihara K (1999) Highly enantioselective catalytic Diels-Alder addition promoted by a chiral bis (oxazoline)-magnesium complex. Tetrahedron Lett 45: 6807-6810.
-
(1999)
Tetrahedron Lett
, vol.45
, pp. 6807-6810
-
-
Corey, E.J.1
Ishihara, K.2
-
21
-
-
0002923489
-
Stereoselective organic synthesis via dynamic kinetic resolution
-
Noyori R, Tokunaga M, Kitamura M (1995) Stereoselective organic synthesis via dynamic kinetic resolution. Bull Chem Soc Jpn 68:36-56.
-
(1995)
Bull Chem Soc Jpn
, vol.68
, pp. 36-56
-
-
Noyori, R.1
Tokunaga, M.2
Kitamura, M.3
-
22
-
-
0037010024
-
Enantiodivergence in small-molecule catalysis of asymmetric phosphorylation: Concise total syntheses of the enantiomeric D-myo-inositol-1-phosphate and D-myo-inositol-3-phosphate
-
Sculimbrene BR, Morgan AJ, Miller SJ (2002) Enantiodivergence in small-molecule catalysis of asymmetric phosphorylation: Concise total syntheses of the enantiomeric D-myo-inositol-1-phosphate and D-myo-inositol-3-phosphate. J Am Chem Soc 124: 11653-11656.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 11653-11656
-
-
Sculimbrene, B.R.1
Morgan, A.J.2
Miller, S.J.3
-
23
-
-
0034807976
-
Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: An approach to kinetic resolution of secondary alcohols of broad structural scope
-
Copeland GT, Miller SJ (2001) Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: An approach to kinetic resolution of secondary alcohols of broad structural scope. J Am Chem Soc 123:6496-6502.
-
(2001)
J Am Chem Soc
, vol.123
, pp. 6496-6502
-
-
Copeland, G.T.1
Miller, S.J.2
-
24
-
-
0005519280
-
Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation (AD). 1. Kinetics
-
Kolb HC, Andersson PG, Sharpless KB (1994) Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation (AD). 1. Kinetics. J Am Chem Soc 116:1278-1291.
-
(1994)
J Am Chem Soc
, vol.116
, pp. 1278-1291
-
-
Kolb, H.C.1
Andersson, P.G.2
Sharpless, K.B.3
-
25
-
-
0035800369
-
CH/p attraction: The origin of enantioselectivity in transfer hydrogenation of aromatic carbonyl compound catalyzed by chiral ?6-arene-ruthenium(II) complexes
-
Yamakawa M, Yamada I, Noyori R (2001) CH/p attraction: The origin of enantioselectivity in transfer hydrogenation of aromatic carbonyl compound catalyzed by chiral ?6-arene-ruthenium(II) complexes. Angew Chem Int Ed 40:2818-2821.
-
(2001)
Angew Chem Int Ed
, vol.40
, pp. 2818-2821
-
-
Yamakawa, M.1
Yamada, I.2
Noyori, R.3
-
26
-
-
0031021995
-
The application of the formyl C-H-O hydrogen bond postulate to the understanding of enantioselective reactions involving chiral boron Lewis acids
-
Corey EJ, Rohde JJ (1997) The application of the formyl C-H-O hydrogen bond postulate to the understanding of enantioselective reactions involving chiral boron Lewis acids. Tetrahedron Lett 38:37-40.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 37-40
-
-
Corey, E.J.1
Rohde, J.J.2
-
27
-
-
0029927729
-
Mutagenesis study of active site residues in chorismate mutase from Bacillus subtilis
-
Cload ST, Liu DR, Pastor RM, Schultz PG (1996)Mutagenesis study of active site residues in chorismate mutase from Bacillus subtilis. J Am Chem Soc 118:1787-1788.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 1787-1788
-
-
Cload, S.T.1
Liu, D.R.2
Pastor, R.M.3
Schultz, P.G.4
-
28
-
-
0029148869
-
Acceleration of a dipolar Claisen rearrangement by hydrogen bonding to a soluble diaryl urea
-
Curran DP, Kuo LH (1995) Acceleration of a dipolar Claisen rearrangement by hydrogen bonding to a soluble diaryl urea. Tetrahedron Lett 36:6647-6650.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 6647-6650
-
-
Curran, D.P.1
Kuo, L.H.2
-
29
-
-
0001193489
-
Synthesis and Claisen rearrangement of alkoxyallyl enol ethers. Evidence for a dipolar transition state
-
Coates RM, Rogers BD, Hobbs SJ, Peck DR, Curran DP (1987) Synthesis and Claisen rearrangement of alkoxyallyl enol ethers. Evidence for a dipolar transition state. J Am Chem Soc 109:1160-1170.
-
(1987)
J Am Chem Soc
, vol.109
, pp. 1160-1170
-
-
Coates, R.M.1
Rogers, B.D.2
Hobbs, S.J.3
Peck, D.R.4
Curran, D.P.5
-
30
-
-
84973100605
-
Effects of hydration on the Claisen rearrangement of allyl vinyl ether from computer simulations
-
Severance DL, Jorgensen WL (1992) Effects of hydration on the Claisen rearrangement of allyl vinyl ether from computer simulations. J Am Chem Soc 114: 10966-10968.
-
(1992)
J Am Chem Soc
, vol.114
, pp. 10966-10968
-
-
Severance, D.L.1
Jorgensen, W.L.2
-
31
-
-
0001718717
-
Transition structure and substituent effects on aqueous acceleration of the Claisen rearrangement
-
Sehgal A, Shao L, Gao J (1995) Transition structure and substituent effects on aqueous acceleration of the Claisen rearrangement. J Am Chem Soc 117:11337-11340.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 11337-11340
-
-
Sehgal, A.1
Shao, L.2
Gao, J.3
-
32
-
-
0000403949
-
What causes aqueous acceleration of the Claisen rearrangement?
-
Cramer CJ, Truhlar DG (1992) What causes aqueous acceleration of the Claisen rearrangement? J Am Chem Soc 114:8794-8799.
-
(1992)
J Am Chem Soc
, vol.114
, pp. 8794-8799
-
-
Cramer, C.J.1
Truhlar, D.G.2
-
33
-
-
47849090006
-
Enantioselective Claisen rearrangements with a hydrogen-bond donor catalyst
-
Uyeda C, Jacobsen EN (2008) Enantioselective Claisen rearrangements with a hydrogen-bond donor catalyst. J Am Chem Soc 130:9228-9229.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 9228-9229
-
-
Uyeda, C.1
Jacobsen, E.N.2
-
34
-
-
0001098701
-
Concerning the effects of aromatic ring fluorination on the cation-p interaction and other molecular recognition phenomenon in aqueous media
-
Ngola SM, Dougherty DA (1998) Concerning the effects of aromatic ring fluorination on the cation-p interaction and other molecular recognition phenomenon in aqueous media. J Org Chem 63:4566-4567.
-
(1998)
J Org Chem
, vol.63
, pp. 4566-4567
-
-
Ngola, S.M.1
Dougherty, D.A.2
-
35
-
-
0029967521
-
Cation-p interactions in simple aromatics: Electrostatics provide a predictive tool
-
Mecozzi S, West AP, Dougherty DA (1996) Cation-p interactions in simple aromatics: electrostatics provide a predictive tool. J Am Chem Soc 118:2307-2308.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 2307-2308
-
-
Mecozzi, S.1
West, A.P.2
Dougherty, D.A.3
-
36
-
-
4344713238
-
Highly enantioselective catalytic acyl-pictet-spengler reactions
-
Taylor MS, Jacobsen EN (2004) Highly enantioselective catalytic acyl-pictet-spengler reactions. J Am Chem Soc 126:10558-10559.
-
(2004)
J Am Chem Soc
, vol.126
, pp. 10558-10559
-
-
Taylor, M.S.1
Jacobsen, E.N.2
-
37
-
-
35948942795
-
Enantioselective Pictet-Spengler-type cyclizations of hydroxylactams: H-bond donor catalysis by anion binding
-
Raheem IT, Thiara PS, Peterson EA, Jacobsen EN (2007) Enantioselective Pictet-Spengler-type cyclizations of hydroxylactams: H-bond donor catalysis by anion binding. J Am Chem Soc 129:13404-13405.
-
(2007)
J Am Chem Soc
, vol.129
, pp. 13404-13405
-
-
Raheem, I.T.1
Thiara, P.S.2
Peterson, E.A.3
Jacobsen, E.N.4
-
38
-
-
44949230317
-
Enantioselective thiourea-catalyzed additions to oxocarbenium ions
-
Reisman SE, Doyle AG, Jacobsen EN (2008) Enantioselective thiourea-catalyzed additions to oxocarbenium ions. J AmChem Soc 130:7198-7199.
-
(2008)
J AmChem Soc
, vol.130
, pp. 7198-7199
-
-
Reisman, S.E.1
Doyle, A.G.2
Jacobsen, E.N.3
-
39
-
-
63049095171
-
(Thio) urea organocatalysis -what can be learnt from anion recognition?
-
Zhang Z, Schreiner PR (2009) (Thio)urea organocatalysis -what can be learnt from anion recognition? Chem Soc Rev 38:1187-1198.
-
(2009)
Chem Soc Rev
, vol.38
, pp. 1187-1198
-
-
Zhang, Z.1
Schreiner, P.R.2
-
40
-
-
77950805314
-
Enantioselective thiourea-catalyzed cationic polycyclizations
-
Knowles RR, Lin S, Jacobsen EN (2010) Enantioselective thiourea-catalyzed cationic polycyclizations. J Am Chem Soc 132:5030-5032.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 5030-5032
-
-
Knowles, R.R.1
Lin, S.2
Jacobsen, E.N.3
-
41
-
-
0037148784
-
Squalene-hopene cyclase: Catalytic mechanism and substrate recognition
-
Hoshino T, Sato T (2002) Squalene-hopene cyclase: Catalytic mechanism and substrate recognition. Chem Commun (Camb) (4):291-301.
-
(2002)
Chem Commun (Camb)
, Issue.4
, pp. 291-301
-
-
Hoshino, T.1
Sato, T.2
-
42
-
-
33749529751
-
Cation-p interaction in the polyolefin cyclization cascade uncovered by incorporating unnatural amino acids into the catalytic sites of squalene cyclase
-
Morikubo N, et al. (2006) Cation-p interaction in the polyolefin cyclization cascade uncovered by incorporating unnatural amino acids into the catalytic sites of squalene cyclase. J Am Chem Soc 128:13184-13194.
-
(2006)
J Am Chem Soc
, vol.128
, pp. 13184-13194
-
-
Morikubo, N.1
-
43
-
-
0030769202
-
Structure and function of a squalene cyclase
-
Wendt KU, Poralla K, Schulz GE (1997) Structure and function of a squalene cyclase. Science 277: 1811-1815.
-
(1997)
Science
, vol.277
, pp. 1811-1815
-
-
Wendt, K.U.1
Poralla, K.2
Schulz, G.E.3
-
44
-
-
8544273685
-
Insight into steroid scaffold formation from the structure of human oxidosqualene cyclase
-
Thoma R, et al. (2004) Insight into steroid scaffold formation from the structure of human oxidosqualene cyclase. Nature 432:118-122.
-
(2004)
Nature
, vol.432
, pp. 118-122
-
-
Thoma, R.1
-
45
-
-
38349134195
-
Exploring the size dependence of cyclic and acyclic p-systems on cation-p binding
-
Vijay D, Sastry GN (2008) Exploring the size dependence of cyclic and acyclic p-systems on cation-p binding. Phys Chem Chem Phys 10:582-590.
-
(2008)
Phys Chem Chem Phys
, vol.10
, pp. 582-590
-
-
Vijay, D.1
Sastry, G.N.2
-
46
-
-
0034801468
-
An enthalpic component in cooperativity: The relationship between enthalpy, entropy, and noncovalent structure in weak associations
-
Calderone CT, Williams DH (2001) An enthalpic component in cooperativity: the relationship between enthalpy, entropy, and noncovalent structure in weak associations. J Am Chem Soc 123:6262-6267.
-
(2001)
J Am Chem Soc
, vol.123
, pp. 6262-6267
-
-
Calderone, C.T.1
Williams, D.H.2
-
47
-
-
0001500053
-
Evidence for the importance of polarizability in biomimetic catalysis involving cyclophane receptors
-
Ngola SM, Dougherty DA (1996) Evidence for the importance of polarizability in biomimetic catalysis involving cyclophane receptors. J Org Chem 61: 4355-4360.
-
(1996)
J Org Chem
, vol.61
, pp. 4355-4360
-
-
Ngola, S.M.1
Dougherty, D.A.2
-
49
-
-
70350329273
-
Mechanism of amidothiourea catalyzed enantioselective imine hydrocyanation: Transition state stabilization via multiple non-covalent interactions
-
Zuend SJ, Jacobsen EN (2009) Mechanism of amidothiourea catalyzed enantioselective imine hydrocyanation: transition state stabilization via multiple non-covalent interactions. J Am ChemSoc 131:15358-15374.
-
(2009)
J Am ChemSoc
, vol.131
, pp. 15358-15374
-
-
Zuend, S.J.1
Jacobsen, E.N.2
-
50
-
-
70350055059
-
Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids
-
Zuend SJ, Coughlin MP, Lalonde MP, Jacobsen EN (2009) Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids. Nature 461:968-970.
-
(2009)
Nature
, vol.461
, pp. 968-970
-
-
Zuend, S.J.1
Coughlin, M.P.2
Lalonde, M.P.3
Jacobsen, E.N.4
-
51
-
-
0033972184
-
Theoretical study of the addition of hydrogen cyanide to methanimine in the gas phase and in aqueous solution
-
Arnaud A, et al. (2000) Theoretical study of the addition of hydrogen cyanide to methanimine in the gas phase and in aqueous solution. J Am Chem Soc 122:324-330.
-
(2000)
J Am Chem Soc
, vol.122
, pp. 324-330
-
-
Arnaud, A.1
-
52
-
-
77149152524
-
Asymmetric cooperative catalysis of strong Brønsted acid-promoted reactions using chiral ureas
-
Xu H, Zuend SJ, Woll MG, Tao Y, Jacobsen EN (2010) Asymmetric cooperative catalysis of strong Brønsted acid-promoted reactions using chiral ureas. Science 327:986-990.
-
(2010)
Science
, vol.327
, pp. 986-990
-
-
Xu, H.1
Zuend, S.J.2
Woll, M.G.3
Tao, Y.4
Jacobsen, E.N.5
-
53
-
-
0031593029
-
NMR spectroscopic evidence for the structure of iminium ion pairs
-
Mayr H, Ofial AR, Wurthwein EU, Aust NC (1997) NMR spectroscopic evidence for the structure of iminium ion pairs. J Am Chem Soc 119:12727-12733.
-
(1997)
J Am Chem Soc
, vol.119
, pp. 12727-12733
-
-
Mayr, H.1
Ofial, A.R.2
Wurthwein, E.U.3
Aust, N.C.4
-
54
-
-
0025230340
-
Enzymic reaction selectivity by negative catalysis or how do enzymes deal with highly reactive interemediates?
-
Retey J (1990) Enzymic reaction selectivity by negative catalysis or how do enzymes deal with highly reactive interemediates? Angew Chem Int Ed Engl 29: 355-361.
-
(1990)
Angew Chem Int Ed Engl
, vol.29
, pp. 355-361
-
-
Retey, J.1
|