-
1
-
-
0035886887
-
Enantioselective Organocatalysis
-
Dalko, P. I.; Moisan, L. Enantioselective Organocatalysis. Angew. Chem., Int. Ed 2001, 40, 3726.
-
(2001)
Angew. Chem., Int. Ed
, vol.40
, pp. 3726
-
-
Dalko, P.I.1
Moisan, L.2
-
5
-
-
33748220015
-
Diastereoselective Enzymatic Aldol Additions: L-rhamnulose and L-fuculose 1-phosphate Aldolases from E. coli
-
Fessner, W. D.; Sinerius, G.; Schneider, A.; Dreyer, M.; Schulz, G. E.; Badia, J.; Aguilar, J. Diastereoselective Enzymatic Aldol Additions: L-rhamnulose and L-fuculose 1-phosphate Aldolases from E. coli. Angew. Chem., Int. Ed. Engl. 1991, 30, 555.
-
(1991)
Angew. Chem., Int. Ed. Engl
, vol.30
, pp. 555
-
-
Fessner, W.D.1
Sinerius, G.2
Schneider, A.3
Dreyer, M.4
Schulz, G.E.5
Badia, J.6
Aguilar, J.7
-
6
-
-
0031313763
-
Enzymes in Organic Synthesis: Recent Developments in Aldol Reactions and Glycosylations
-
Takayama, S.; McGarvey, G. J.; Wong, C. H. Enzymes in Organic Synthesis: Recent Developments in Aldol Reactions and Glycosylations. Chem. Soc. Rev. 1997, 26, 405.
-
(1997)
Chem. Soc. Rev
, vol.26
, pp. 405
-
-
Takayama, S.1
McGarvey, G.J.2
Wong, C.H.3
-
8
-
-
0001373188
-
Enzyme Catalyzed Synthesis of Carbohydrates
-
Toone, E. J.; Simon, E. S.; Bednarski, M. D.; Whitesides, G. M. Enzyme Catalyzed Synthesis of Carbohydrates. Tetrahedron 1989, 45, 5365.
-
(1989)
Tetrahedron
, vol.45
, pp. 5365
-
-
Toone, E.J.1
Simon, E.S.2
Bednarski, M.D.3
Whitesides, G.M.4
-
10
-
-
2642642035
-
Recent Advances in the Chemoenzymatic Synthesis of Carbohydrates and Carbohydrate Mimetics
-
Gijsen, H. J. M.; Qiao, L.; Fitz, W. G.; Wong, C. H. Recent Advances in the Chemoenzymatic Synthesis of Carbohydrates and Carbohydrate Mimetics. Chem. Rev. 1996, 96, 443.
-
(1996)
Chem. Rev
, vol.96
, pp. 443
-
-
Gijsen, H.J.M.1
Qiao, L.2
Fitz, W.G.3
Wong, C.H.4
-
11
-
-
0037471649
-
Carbon-Carbon Bonds by Hydrolytic Enzymes
-
Branneby, C.; Carlqvist, P.; Magnusson, A.; Huit, K.; Brinck, T.; Berglund, P. Carbon-Carbon Bonds by Hydrolytic Enzymes. J. Am. Chem. Soc. 2003, 125, 874.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 874
-
-
Branneby, C.1
Carlqvist, P.2
Magnusson, A.3
Huit, K.4
Brinck, T.5
Berglund, P.6
-
12
-
-
33745893522
-
Direct Asymmetric Intermolecular Aldol Reactions Catalyzed by Amino Acids and Small Peptides
-
Cǒrdova, A.; Zou, W. B.; Dziedzic, P.; Ibrahem, I.; Reyes, E.; Xu, Y. M. Direct Asymmetric Intermolecular Aldol Reactions Catalyzed by Amino Acids and Small Peptides. Chem.-Eur. J. 2006, 12, 5383.
-
(2006)
Chem.-Eur. J
, vol.12
, pp. 5383
-
-
Cǒrdova, A.1
Zou, W.B.2
Dziedzic, P.3
Ibrahem, I.4
Reyes, E.5
Xu, Y.M.6
-
13
-
-
0002350948
-
Enzymatic C-C Bond Formation in Asymmetric Synthesis
-
Fessner, W.-D.; Walter, C. Enzymatic C-C Bond Formation in Asymmetric Synthesis. Top. Curr. Chem. 1996, 184, 97.
-
(1996)
Top. Curr. Chem
, vol.184
, pp. 97
-
-
Fessner, W.-D.1
Walter, C.2
-
14
-
-
0034812506
-
Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions
-
Sakthivel, K.; Notz, W. G.; Bui, T.; Barbas, C. F. Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions. J. Am. Chem. Soc. 2001, 123, 5260.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 5260
-
-
Sakthivel, K.1
Notz, W.G.2
Bui, T.3
Barbas, C.F.4
-
15
-
-
0037164621
-
Proline-catalyzed Asymmetric Assembly Reactions: Enzyme-like Assembly of Carbohydrates and Polyketides from Three Aldehyde Substrates
-
Chowdari, N. S.; Ramacbary, D. B.; Córdova, A.; Barbas, C. F. Proline-catalyzed Asymmetric Assembly Reactions: Enzyme-like Assembly of Carbohydrates and Polyketides from Three Aldehyde Substrates. Tetrahedron Lett. 2002, 43, 9591.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 9591
-
-
Chowdari, N.S.1
Ramacbary, D.B.2
Córdova, A.3
Barbas, C.F.4
-
16
-
-
0038375490
-
Fluorescent Detection of Carbon-carbon Bond Formation
-
Tanaka, F.; Thayumanavan, R.; Barbas, C. F., III. Fluorescent Detection of Carbon-carbon Bond Formation. J. Am. Chem. Soc. 2003, 125, 8523.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 8523
-
-
Tanaka, F.1
Thayumanavan, R.2
Barbas III, C.F.3
-
17
-
-
1642386775
-
Current Progress in the Asymmetric Aldol Addition Reaction
-
Palomo, C.; Oiarbide, M.; García, J. M. Current Progress in the Asymmetric Aldol Addition Reaction. Chem. Soc. Rev. 2004, 33, 65.
-
(2004)
Chem. Soc. Rev
, vol.33
, pp. 65
-
-
Palomo, C.1
Oiarbide, M.2
García, J.M.3
-
18
-
-
0032733360
-
Organic Synthesis Supported by Antibody Catalysis
-
Hasserodt, J. Organic Synthesis Supported by Antibody Catalysis. Synlett. 1999, 12, 2007.
-
(1999)
Synlett
, vol.12
, pp. 2007
-
-
Hasserodt, J.1
-
19
-
-
0034812506
-
Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions
-
Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F., III. Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions. J. Am. Chem. Soc. 2001, 123, 5260.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 5260
-
-
Sakthivel, K.1
Notz, W.2
Bui, T.3
Barbas III, C.F.4
-
20
-
-
17044437071
-
Reevaluation of the Mechanism of the Baylis Hillman Reaction: Implications for Asymmetric Catalysis
-
Aggarwal, V. K.; Fulford, S. Y.; Lloyd-Jones, G. C. Reevaluation of the Mechanism of the Baylis Hillman Reaction: Implications for Asymmetric Catalysis. Angew. Chem., Int. Ed 2005, 44, 1706.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 1706
-
-
Aggarwal, V.K.1
Fulford, S.Y.2
Lloyd-Jones, G.C.3
-
21
-
-
18844456318
-
Development of Small Designer Aldolase Enzymes: Catalytic Activity, Folding, and Substrate Specificity
-
Tanaka, F.; Fuller, R.; Barbas, C. F. Development of Small Designer Aldolase Enzymes: Catalytic Activity, Folding, and Substrate Specificity. Biochemistry 2005, 44, 7583.
-
(2005)
Biochemistry
, vol.44
, pp. 7583
-
-
Tanaka, F.1
Fuller, R.2
Barbas, C.F.3
-
22
-
-
0033908031
-
Man-made Enzymes-from Design to in Vitro Compartmentalization
-
Griffiths, A. D.; Tawfik, D. S. Man-made Enzymes-from Design to in Vitro Compartmentalization. Curr. Opin. Bioteck 2000, 11, 338.
-
(2000)
Curr. Opin. Bioteck
, vol.11
, pp. 338
-
-
Griffiths, A.D.1
Tawfik, D.S.2
-
23
-
-
24944439888
-
Polyamino Acids as Aynthetic Enzymes: Mechanism, Applications and Relevance to Prebiotic Catalysis
-
Carrea, G.; Colonna, S.; Kelly, D. R.; Lazcano, A.; Ottolina, G.; Roberts, S. M. Polyamino Acids as Aynthetic Enzymes: Mechanism, Applications and Relevance to Prebiotic Catalysis. Trends Biotechnol. 2005, 23, 507.
-
(2005)
Trends Biotechnol
, vol.23
, pp. 507
-
-
Carrea, G.1
Colonna, S.2
Kelly, D.R.3
Lazcano, A.4
Ottolina, G.5
Roberts, S.M.6
-
24
-
-
0034599654
-
A General Catalyst for the Asymmetric Strecker Reaction
-
Jacobsen, E. N.; Sigman, M. S.; Vachal, P. A General Catalyst for the Asymmetric Strecker Reaction. Angew. Chem., Int. Ed 2000, 39, 1279.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 1279
-
-
Jacobsen, E.N.1
Sigman, M.S.2
Vachal, P.3
-
25
-
-
0034675660
-
Asymmetric Conjugate Addition of Azide to α, β-Unsaturated Carbonyl Compounds Catalyzed by Simple Peptides
-
Horstmann, T. E.; Guerin, D. J.; Miller, S. J. Asymmetric Conjugate Addition of Azide to α, β-Unsaturated Carbonyl Compounds Catalyzed by Simple Peptides. Angew. Chem, Int. Ed 2000, 39, 3635.
-
(2000)
Angew. Chem, Int. Ed
, vol.39
, pp. 3635
-
-
Horstmann, T.E.1
Guerin, D.J.2
Miller, S.J.3
-
26
-
-
0035904415
-
Discoverty of a Catalytic Asymmetric Phosphorylations through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of D-myo-Inositol-1-Phosphate
-
Sculimbrene, B. R.; Miller, S. J. Discoverty of a Catalytic Asymmetric Phosphorylations through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of D-myo-Inositol-1-Phosphate. J. Am. Chem Soc. 2001, 123, 10125.
-
(2001)
J. Am. Chem Soc
, vol.123
, pp. 10125
-
-
Sculimbrene, B.R.1
Miller, S.J.2
-
27
-
-
0035969617
-
Highly Enantioselective Enone Epoxidation Catalyzed by Short Solid Phase-Bound Peptides: Dominant Role of Peptide Helicity
-
Berkessel, A.; Gasch, N.; Alaubitz, K.; Koch, C. Highly Enantioselective Enone Epoxidation Catalyzed by Short Solid Phase-Bound Peptides: Dominant Role of Peptide Helicity. Org. Lett. 2001, 3, 3839.
-
(2001)
Org. Lett
, vol.3
, pp. 3839
-
-
Berkessel, A.1
Gasch, N.2
Alaubitz, K.3
Koch, C.4
-
28
-
-
0043166704
-
Enantioselective Direct Aldol Addition of Acetone to Aliphatic Aldehydes
-
Szöllösi, G.; London, G.; Baláspiri, L.; Somlai, C.; Bartók, M. Enantioselective Direct Aldol Addition of Acetone to Aliphatic Aldehydes. Chirality 2003, 15, S90.
-
(2003)
Chirality
, vol.15
-
-
Szöllösi, G.1
London, G.2
Baláspiri, L.3
Somlai, C.4
Bartók, M.5
-
29
-
-
33746216402
-
Functionalized Chiral Ionic Liquids as Highly Efficient Asymmetric Organocatalysts for Michael Addition to Nitroolefins
-
Luo, S. Z; Mi, X. L.; Zhang, L.; Liu, S.; Xu, H.; Cheng, J. P. Functionalized Chiral Ionic Liquids as Highly Efficient Asymmetric Organocatalysts for Michael Addition to Nitroolefins. Angew. Chem., Int. Ed. 2006, 45, 3093.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 3093
-
-
Luo, S.Z.1
Mi, X.L.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.P.6
-
30
-
-
9944253349
-
Glucose Oxidasemagnetite Nanoparticle Bioconjugate for Glucose Sensing
-
Rossi, L. M.; Quach, A. D.; Rosenzweig, Z. Glucose Oxidasemagnetite Nanoparticle Bioconjugate for Glucose Sensing. Anal. Bioanal Chem. 2004, 380, 606.
-
(2004)
Anal. Bioanal Chem
, vol.380
, pp. 606
-
-
Rossi, L.M.1
Quach, A.D.2
Rosenzweig, Z.3
-
31
-
-
33645235787
-
Activity of Magnetite Immobilized Catalase in Hydrogen Peroxide Decomposition
-
Horst, F; Rueda, E. H.; Ferreira, M. L. Activity of Magnetite Immobilized Catalase in Hydrogen Peroxide Decomposition. Enzyme Microb. Technol. 2006, 38, 1005.
-
(2006)
Enzyme Microb. Technol
, vol.38
, pp. 1005
-
-
Horst, F.1
Rueda, E.H.2
Ferreira, M.L.3
-
32
-
-
33646468489
-
Asymmetric Catalysis by Chiral Hydrogen-bond Donors
-
Taylor, M. S.; Jacobsen, E. N. Asymmetric Catalysis by Chiral Hydrogen-bond Donors. Angew. Chem., Int. Ed. 2006, 45, 1520.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 1520
-
-
Taylor, M.S.1
Jacobsen, E.N.2
-
33
-
-
0000034575
-
Ionic Liquids-New Solutions for Transition Metal Catalysis
-
Wasserscheid, P.; Keim, W. Ionic Liquids-New Solutions for Transition Metal Catalysis. Angew. Chem., Int. Ed. 2000, 39, 3772.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 3772
-
-
Wasserscheid, P.1
Keim, W.2
-
34
-
-
0347417134
-
Room Temperature Ionic Liquids Solvents for Synthesis and Catalysis
-
Welton, T. Room Temperature Ionic Liquids Solvents for Synthesis and Catalysis. Chem. Rev. 1999, 99, 2071.
-
(1999)
Chem. Rev
, vol.99
, pp. 2071
-
-
Welton, T.1
-
35
-
-
4244039329
-
Ionic liquids: Perspectives for Organic and Catalytic Reactions
-
Olivier-Bourbigou, H.; Magna, L. Ionic liquids: Perspectives for Organic and Catalytic Reactions. J. Mol. Catal A: Chem. 2002, 182-183, 419.
-
(2002)
J. Mol. Catal A: Chem
, vol.182-183
, pp. 419
-
-
Olivier-Bourbigou, H.1
Magna, L.2
-
36
-
-
33748844804
-
Solvent Extraction of Strontium Nitrate by a Crown Ether Using Room-Temperature Ionic Liquids
-
Dai, S.; Ju, Y. H.; Barnes, C. E. Solvent Extraction of Strontium Nitrate by a Crown Ether Using Room-Temperature Ionic Liquids. J. Chem. Soc. Dalton. Trans. I. 1999, 8, 1201.
-
(1999)
J. Chem. Soc. Dalton. Trans
, vol.1
, Issue.8
, pp. 1201
-
-
Dai, S.1
Ju, Y.H.2
Barnes, C.E.3
-
37
-
-
28044432333
-
Cysteine-derived Organocatalyst in a Highly Enantioselective Intramolecular Michael Reaction
-
Hayashi, Y.; Gotoh, H.; Tamura, T.; Yamaguchi, H.; Masui, R.; Shoji, M. Cysteine-derived Organocatalyst in a Highly Enantioselective Intramolecular Michael Reaction. J. Am. Chem. Soc. 2005, 127, 16028.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 16028
-
-
Hayashi, Y.1
Gotoh, H.2
Tamura, T.3
Yamaguchi, H.4
Masui, R.5
Shoji, M.6
-
38
-
-
12844278819
-
Imidazolinium Salts as Catalysts for the Aza-Diels-Alder Reaction
-
Jurčík, V.; Wilhelm, R. Imidazolinium Salts as Catalysts for the Aza-Diels-Alder Reaction. Org. Biomol. Chem. 2005, 3, 239.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 239
-
-
Jurčík, V.1
Wilhelm, R.2
-
39
-
-
11844302258
-
Enantioand Diastereoselective Michael Reaction of 1,3-Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional Thiourea
-
Okino, T.; Hoashi, Y.; Furukawa, T.; Xu, X.; Takemoto, Y. Enantioand Diastereoselective Michael Reaction of 1,3-Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional Thiourea. J. Am. Chem. Soc. 2005, 127, 119.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 119
-
-
Okino, T.1
Hoashi, Y.2
Furukawa, T.3
Xu, X.4
Takemoto, Y.5
-
40
-
-
0029109703
-
Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition (Part 1)
-
Wong, C. H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto, T. Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition (Part 1). Angew. Chem., Int. Ed. Engl. 1995, 34, 412.
-
(1995)
Angew. Chem., Int. Ed. Engl
, vol.34
, pp. 412
-
-
Wong, C.H.1
Halcomb, R.L.2
Ichikawa, Y.3
Kajimoto, T.4
-
42
-
-
0033605909
-
Enantioselective Reduction of Ketones Examination of Bifunctional Ligands
-
Sibi, M. P.; Cook, G. R.; Liu, P. Enantioselective Reduction of Ketones Examination of Bifunctional Ligands. Tetrahedron Lett. 1999, 40, 2477.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 2477
-
-
Sibi, M.P.1
Cook, G.R.2
Liu, P.3
-
43
-
-
4143095871
-
Enamine Catalysis is a Powerful Strategy for the Catalytic Generation and Use of Carbanion Equivalents
-
List, B. Enamine Catalysis is a Powerful Strategy for the Catalytic Generation and Use of Carbanion Equivalents. Acc Chem. Res. 2004, 37, 548.
-
(2004)
Acc Chem. Res
, vol.37
, pp. 548
-
-
List, B.1
-
44
-
-
20344372440
-
An Ionic Liquid Influenced 1-proline Catalysed Asymmetric Michael Addition of Ketones to Nitrostyrene
-
Rasalkar, M. S.; Potdar, M. K.; Mohile, S. S.; Salunkhe, M. M. An Ionic Liquid Influenced 1-proline Catalysed Asymmetric Michael Addition of Ketones to Nitrostyrene. J. Mol. Catal. A: Chem. 2005, 235, 267.
-
(2005)
J. Mol. Catal. A: Chem
, vol.235
, pp. 267
-
-
Rasalkar, M.S.1
Potdar, M.K.2
Mohile, S.S.3
Salunkhe, M.M.4
-
45
-
-
5344224096
-
Towards Perfect Catalytic Asymmetric Synmesis: Dual Activation of the Electrophile and the Nucleophile
-
Ma, J. A.; Cahard, D. Towards Perfect Catalytic Asymmetric Synmesis: Dual Activation of the Electrophile and the Nucleophile. Angew. Chem., Int. Ed. 2004, 43, 4566.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 4566
-
-
Ma, J.A.1
Cahard, D.2
-
46
-
-
0035313630
-
Biocatalytic Modification of Natural Products
-
Riva, S. Biocatalytic Modification of Natural Products. Curr. Opin. Chem. Biol. 2001, 5, 106.
-
(2001)
Curr. Opin. Chem. Biol
, vol.5
, pp. 106
-
-
Riva, S.1
-
47
-
-
0001396912
-
Enzyme-mediated Regioselective Acylation of Polyhydroxylated Natural Products
-
Danieli, B.; Riva, S. Enzyme-mediated Regioselective Acylation of Polyhydroxylated Natural Products. Pure Appl. Chem. 1994, 66, 2215.
-
(1994)
Pure Appl. Chem
, vol.66
, pp. 2215
-
-
Danieli, B.1
Riva, S.2
-
48
-
-
0542421525
-
-
Gellman, S. H. Foldamers: A Manifesto. Acc. Chem. Res. 1998, 37, 173.
-
Gellman, S. H. Foldamers: A Manifesto. Acc. Chem. Res. 1998, 37, 173.
-
-
-
-
49
-
-
34247131307
-
Enzyme Promiscuity: Mechanism and Applications
-
Huit, K.; Berglund, P. Enzyme Promiscuity: Mechanism and Applications. Trends Biotechnol. 2007, 25, 231.
-
(2007)
Trends Biotechnol
, vol.25
, pp. 231
-
-
Huit, K.1
Berglund, P.2
-
50
-
-
0042379938
-
-
Gennari, C.; Piarulli, U. Combinatorial Libraries of Chiral Ligands for Eantioselective Catalysis. Chem. Rev. 2003, 103, 3071.
-
Gennari, C.; Piarulli, U. Combinatorial Libraries of Chiral Ligands for Eantioselective Catalysis. Chem. Rev. 2003, 103, 3071.
-
-
-
-
51
-
-
0000486957
-
Kombinatorische und Evolutionsgesteuerte Methoden zur Bildung Enantioselektiver Katalysatoren.
-
Reetz, M. T. Kombinatorische und Evolutionsgesteuerte Methoden zur Bildung Enantioselektiver Katalysatoren. Angew. Chem. 2001, 113, 292.
-
(2001)
Angew. Chem
, vol.113
, pp. 292
-
-
Reetz, M.T.1
-
52
-
-
0001704546
-
Super-High-ThroughputScreening chiraler Liganden und Aktivatoren: Asymmetrische Aktivierung chiraler Diol-Zink-Katalysatoren durch Chirale Stickstoffaktivatoren für the Enantioselektive Addition von Diethylzink an Aldehyde
-
Ding, K. L.; Ishii, A.; Mikami, K. Super-High-ThroughputScreening chiraler Liganden und Aktivatoren: Asymmetrische Aktivierung chiraler Diol-Zink-Katalysatoren durch Chirale Stickstoffaktivatoren für the Enantioselektive Addition von Diethylzink an Aldehyde. Angew. Chem. 1999, 111, 519.
-
(1999)
Angew. Chem
, vol.111
, pp. 519
-
-
Ding, K.L.1
Ishii, A.2
Mikami, K.3
-
53
-
-
0742303085
-
Preparation and Characterization of Amino-silane Modified Superparamagnetic Silica Nanospheres
-
Liu, X. Q.; Ma, Z. Y.; Xing, J. M.; Liu, H. Z. Preparation and Characterization of Amino-silane Modified Superparamagnetic Silica Nanospheres. J. Magn. Magn. Mater. 2004, 270, 1.
-
(2004)
J. Magn. Magn. Mater
, vol.270
, pp. 1
-
-
Liu, X.Q.1
Ma, Z.Y.2
Xing, J.M.3
Liu, H.Z.4
-
54
-
-
0037442620
-
3 Magnetic Nanoparticles
-
3 Magnetic Nanoparticles. J. Am. Chem. Soc. 2003, 125, 1684.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 1684
-
-
Dyal, A.1
Loos, K.2
Noto, M.3
Chang, S.W.4
Spagnoli, C.5
Shafi, K.V.P.M.6
Ulman, A.7
Cowman, M.8
Gross, R.A.9
-
55
-
-
0001463016
-
Enantioselective Aldol Reaction with an Artificial Aldolase Assembled from a Primary Amine and an Antibody
-
Reymond, J. L.; Chen, Y. W. Enantioselective Aldol Reaction with an Artificial Aldolase Assembled from a Primary Amine and an Antibody. J. Org. Chem. 1995, 60, 6970.
-
(1995)
J. Org. Chem
, vol.60
, pp. 6970
-
-
Reymond, J.L.1
Chen, Y.W.2
-
56
-
-
0035843132
-
Enabling the Chemistry of Life
-
Walsh, C. Enabling the Chemistry of Life. Nature 2001, 409, 226.
-
(2001)
Nature
, vol.409
, pp. 226
-
-
Walsh, C.1
-
57
-
-
3142613216
-
Catalytic Direct Asymmetric Michael Reactions: Addition of Unmodified Ketone and Aldehyde Donors to Alkylidene Malonates and Nitro Olefins
-
Betancort, J. M.; Sakthivel, K.; Thayumanavan, R.; Tanaka, F.; Barbas, C. F. III. Catalytic Direct Asymmetric Michael Reactions: Addition of Unmodified Ketone and Aldehyde Donors to Alkylidene Malonates and Nitro Olefins. Synthesis 2004, 1509.
-
(2004)
Synthesis
, pp. 1509
-
-
Betancort, J.M.1
Sakthivel, K.2
Thayumanavan, R.3
Tanaka, F.4
Barbas III, C.F.5
-
58
-
-
0000220483
-
Diamine-Catalyzed Asymmetric Michael Additions of Aldehydes and Ketones to Nitrostyrene
-
Alexakis, A.; Andrey, O. Diamine-Catalyzed Asymmetric Michael Additions of Aldehydes and Ketones to Nitrostyrene. Org. Lett. 2002, 4, 3611.
-
(2002)
Org. Lett
, vol.4
, pp. 3611
-
-
Alexakis, A.1
Andrey, O.2
-
59
-
-
0035843166
-
Improving Enzymes by Using Them in Organic Solvents
-
Klibanov, A. M. Improving Enzymes by Using Them in Organic Solvents. Nature 2001, 409, 241.
-
(2001)
Nature
, vol.409
, pp. 241
-
-
Klibanov, A.M.1
-
60
-
-
0034812506
-
Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions
-
Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F., III. Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-carbon Bond-forming Reactions. J. Am. Chem. Soc. 2001, 123, 5260.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 5260
-
-
Sakthivel, K.1
Notz, W.2
Bui, T.3
Barbas III, C.F.4
-
61
-
-
2942611657
-
Catalyzed Reactions of Acyl Anion Equivalents
-
Johnson, J. S. Catalyzed Reactions of Acyl Anion Equivalents. Angew. Chem., Int. Ed. 2004, 43, 1326.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 1326
-
-
Johnson, J.S.1
-
62
-
-
4143051292
-
Nucleophilic Carbenes in Asymmetric Organocatalysis
-
Enders, D.; Balensiefer, T. Nucleophilic Carbenes in Asymmetric Organocatalysis. Ace Chem. Res. 2004, 37, 534.
-
(2004)
Ace Chem. Res
, vol.37
, pp. 534
-
-
Enders, D.1
Balensiefer, T.2
-
63
-
-
24944586038
-
Proton Affinities of N-heterocyclic Carbene Super Bases
-
Chen, H.; Justes, D. R.; Cooks, G. R. Proton Affinities of N-heterocyclic Carbene Super Bases. Org. Lett. 2005, 7, 3949.
-
(2005)
Org. Lett
, vol.7
, pp. 3949
-
-
Chen, H.1
Justes, D.R.2
Cooks, G.R.3
-
64
-
-
0034607765
-
Dynamic Kinetic Resolution: Synthesis of Optically Active α-amino Acid Derivatives
-
Brown, S. A.; Parker, M.-C.; Turner, N. J. Dynamic Kinetic Resolution: Synthesis of Optically Active α-amino Acid Derivatives. Tetrahedron: Asymmetr. 2000, 11, 1687.
-
(2000)
Tetrahedron: Asymmetr
, vol.11
, pp. 1687
-
-
Brown, S.A.1
Parker, M.-C.2
Turner, N.J.3
-
65
-
-
21344448826
-
Room Temperature Ionic Liquids: Different Classes and Physical Properties
-
Handy, S. T. Room Temperature Ionic Liquids: Different Classes and Physical Properties. Curr. Org. Chem. 2005, 9, 959.
-
(2005)
Curr. Org. Chem
, vol.9
, pp. 959
-
-
Handy, S.T.1
-
66
-
-
17844393084
-
Synthesis of 3-(4tert- butylphenyl)-2-propen-1-one, A precursor to Lilial (R), via an Aldol Condensation in an Ionic Liquid
-
Davey, P. N.; Forsyth, S.; Gunaratne, H.; Hardacre, C.; McKeown, A.; McMath, S. E. J.; Rooney, D. W.; Seddon, K. R. Synthesis of 3-(4tert- butylphenyl)-2-propen-1-one, A precursor to Lilial (R), via an Aldol Condensation in an Ionic Liquid. Green Chem. 2005, 7, 224.
-
(2005)
Green Chem
, vol.7
, pp. 224
-
-
Davey, P.N.1
Forsyth, S.2
Gunaratne, H.3
Hardacre, C.4
McKeown, A.5
McMath, S.E.J.6
Rooney, D.W.7
Seddon, K.R.8
-
67
-
-
0034358478
-
The Julia-Colonna Type Asymmetric Epoxidation Reaction Catalyzed by Soluble Oligo-L-leucines Containing an Alpha-aminoisobutyric Acid Residue: Importance of Helical Structure of the Catalyst on Asymmetric Induction
-
(a) Takagi, R.; Shiraki, A.; Manabe, T.; Kojima, S.; Ohkata, K. The Julia-Colonna Type Asymmetric Epoxidation Reaction Catalyzed by Soluble Oligo-L-leucines Containing an Alpha-aminoisobutyric Acid Residue: Importance of Helical Structure of the Catalyst on Asymmetric Induction. Chem. Lett. 2000, 366.
-
(2000)
Chem. Lett
, pp. 366
-
-
Takagi, R.1
Shiraki, A.2
Manabe, T.3
Kojima, S.4
Ohkata, K.5
-
68
-
-
0033799793
-
The Julia-Colonna Asymmetric Epoxidation Reaction of Chalcone Catalyzed by Lengtíi Defined Oligo-L-leucine: Importance of the N-terminal Functional Group and Helical Structure of the Catalyst in the Asymmetric Induction
-
(b) Takagi, R.; Manabe, T.; Shiraki, A.; Yoneshige, A.; Hiraga, J.; Kojima, S.; Ohkata, K. The Julia-Colonna Asymmetric Epoxidation Reaction of Chalcone Catalyzed by Lengtíi Defined Oligo-L-leucine: Importance of the N-terminal Functional Group and Helical Structure of the Catalyst in the Asymmetric Induction. Bull. Chem. Soc. Jpn. 2000, 73, 2115.
-
(2000)
Bull. Chem. Soc. Jpn
, vol.73
, pp. 2115
-
-
Takagi, R.1
Manabe, T.2
Shiraki, A.3
Yoneshige, A.4
Hiraga, J.5
Kojima, S.6
Ohkata, K.7
-
69
-
-
33644594477
-
Oligopeptides as Catalysts for Asymmetric Epoxidation
-
Kelly, D. R.; Roberts, S. M. Oligopeptides as Catalysts for Asymmetric Epoxidation. Biopolym. (Peptide Sci.) 2006, 84, 74.
-
(2006)
Biopolym. (Peptide Sci.)
, vol.84
, pp. 74
-
-
Kelly, D.R.1
Roberts, S.M.2
-
70
-
-
6044269452
-
In the Golden Age of Organocatalysis
-
Dalko, P. I.; Moisan, L. In the Golden Age of Organocatalysis. Angew. Chem., Int. Ed. 2004, 43, 5138.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5138
-
-
Dalko, P.I.1
Moisan, L.2
-
71
-
-
33646880434
-
Synthetic and Theoretical Study on Proline-catalyzed Knoevenagel Condensation in Ionic Liquid
-
Wang, Y.; Shang, Z. C.; Wu, T. X.; Fan, J. C.; Chen, X. Synthetic and Theoretical Study on Proline-catalyzed Knoevenagel Condensation in Ionic Liquid. J. Mol. Catal. A: Chem. 2006, 253, 212.
-
(2006)
J. Mol. Catal. A: Chem
, vol.253
, pp. 212
-
-
Wang, Y.1
Shang, Z.C.2
Wu, T.X.3
Fan, J.C.4
Chen, X.5
-
72
-
-
20344372440
-
An Ionic Liquid Influenced 1-proline Catalysed Asymmetric Michael Addition of Ketones to Nitrostyrene
-
Rasalkar, M. S.; Potdar, M. K.; Mohile, S. S.; Salunkhe, M. M. An Ionic Liquid Influenced 1-proline Catalysed Asymmetric Michael Addition of Ketones to Nitrostyrene. J. Mol. Catal. A: Chem. 2005, 235, 267.
-
(2005)
J. Mol. Catal. A: Chem
, vol.235
, pp. 267
-
-
Rasalkar, M.S.1
Potdar, M.K.2
Mohile, S.S.3
Salunkhe, M.M.4
-
73
-
-
0034654216
-
Proline-catalyzed Direct Asymmetric Aldol Reactions
-
List, B.; Lerner, R. A.; Barbas, C. F., III. Proline-catalyzed Direct Asymmetric Aldol Reactions. J. Am. Chem. Soc. 2000, 122, 2395.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 2395
-
-
List, B.1
Lerner, R.A.2
Barbas III, C.F.3
-
75
-
-
26944488346
-
Ionic Liquids: Novel Solvents for Petroleum Asphaltenes
-
Liu, Y. S.; Hu, Y. F; Wang, H. B.; Xu, C. M.; Ji, D. J.; Sun, Y.; Guo, T. M. Ionic Liquids: Novel Solvents for Petroleum Asphaltenes. Chin. J. Chem. Eng. 2005, 8, 564.
-
(2005)
Chin. J. Chem. Eng
, vol.8
, pp. 564
-
-
Liu, Y.S.1
Hu, Y.F.2
Wang, H.B.3
Xu, C.M.4
Ji, D.J.5
Sun, Y.6
Guo, T.M.7
-
76
-
-
0347757269
-
Extractive Desulfurization and Denitrogenation of Fuels Using Ionic Liquids
-
Zhang, S. G.; Zhang, Q. L.; Zhang, Z. C. Extractive Desulfurization and Denitrogenation of Fuels Using Ionic Liquids. Ind. Eng. Chem. Res. 2004, 43, 614.
-
(2004)
Ind. Eng. Chem. Res
, vol.43
, pp. 614
-
-
Zhang, S.G.1
Zhang, Q.L.2
Zhang, Z.C.3
-
77
-
-
0029590066
-
Efficient Aldolase Catalytic Antibodies That Use the Enamine Mechanism of Natural Enzymes
-
Wagner, J.; Lerner, R. A.; Barbas, C. Efficient Aldolase Catalytic Antibodies That Use the Enamine Mechanism of Natural Enzymes. Science 1995, 270, 1797.
-
(1995)
Science
, vol.270
, pp. 1797
-
-
Wagner, J.1
Lerner, R.A.2
Barbas, C.3
-
78
-
-
0347417134
-
Room Temperature Ionic Liquids Solvents for Synthesis and Catalysis
-
Welton, T. Room Temperature Ionic Liquids Solvents for Synthesis and Catalysis. Chem. Rev. 1999, 99, 2071.
-
(1999)
Chem. Rev
, vol.99
, pp. 2071
-
-
Welton, T.1
-
79
-
-
0001963457
-
Immobilised Ionic Liquids as Lewis Acid Catalysts for the Alkylation of Aromatic Compounds with Dodecene
-
DeCastro, C.; Sauvage, E.; Valkenberg, M. H.; Holderich, W. F. Immobilised Ionic Liquids as Lewis Acid Catalysts for the Alkylation of Aromatic Compounds with Dodecene. J. Catal. 2000, 196, 86.
-
(2000)
J. Catal
, vol.196
, pp. 86
-
-
DeCastro, C.1
Sauvage, E.2
Valkenberg, M.H.3
Holderich, W.F.4
-
80
-
-
0034678591
-
The Catalytic Asymmetric Aldol Reaction
-
Machajewski, T. D.; Wong, C. H. The Catalytic Asymmetric Aldol Reaction. Angew. Chem., Int. Ed. 2000, 39, 1352.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 1352
-
-
Machajewski, T.D.1
Wong, C.H.2
-
81
-
-
0035804968
-
Polyethylene glycol)-supported Bisoxazolines as Ligands for Catalytic Enantioselective Synthesis
-
Annunziata, R.; Benaglia, M.; Cinquini, M.; Cozzi, F.; Pitillo, M. Polyethylene glycol)-supported Bisoxazolines as Ligands for Catalytic Enantioselective Synthesis. J. Org. Chem. 2001, 66, 3160.
-
(2001)
J. Org. Chem
, vol.66
, pp. 3160
-
-
Annunziata, R.1
Benaglia, M.2
Cinquini, M.3
Cozzi, F.4
Pitillo, M.5
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