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Volumn 49, Issue 6, 2016, Pages 1292-1301

The Development of Multidimensional Analysis Tools for Asymmetric Catalysis and beyond

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EID: 84975797428     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.6b00194     Document Type: Article
Times cited : (304)

References (60)
  • 1
    • 78650585984 scopus 로고    scopus 로고
    • Attractive Noncovalent Interactions in Asymmetric Catalysis: Links between Enzymes and Small Molecule Catalysts
    • Knowles, R. R.; Jacobsen, E. N. Attractive Noncovalent Interactions in Asymmetric Catalysis: Links between Enzymes and Small Molecule Catalysts Proc. Natl. Acad. Sci. U. S. A. 2010, 107, 20678-20685 10.1073/pnas.1006402107
    • (2010) Proc. Natl. Acad. Sci. U. S. A. , vol.107 , pp. 20678-20685
    • Knowles, R.R.1    Jacobsen, E.N.2
  • 2
    • 0003554758 scopus 로고    scopus 로고
    • Schiff base catalysts for the asymmetric Strecker reaction identified and optimized from parallel synthetic libraries
    • Sigman, M. S.; Jacobsen, E. N. Schiff base catalysts for the asymmetric Strecker reaction identified and optimized from parallel synthetic libraries J. Am. Chem. Soc. 1998, 120, 4901-4902 10.1021/ja980139y
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4901-4902
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 3
    • 0037090667 scopus 로고    scopus 로고
    • New methods for the high-throughput screening of enantioselective catalysts and biocatalysts
    • Reetz, M. T. New methods for the high-throughput screening of enantioselective catalysts and biocatalysts Angew. Chem., Int. Ed. 2002, 41, 1335-1338 10.1002/1521-3773(20020415)41:8<1335::AID-ANIE1335>3.0.CO;2-A
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1335-1338
    • Reetz, M.T.1
  • 4
    • 80052629313 scopus 로고    scopus 로고
    • A Simple, Multidimensional Approach to High-Throughput Discovery of Catalytic Reactions
    • Robbins, D. W.; Hartwig, J. F. A Simple, Multidimensional Approach to High-Throughput Discovery of Catalytic Reactions Science 2011, 333, 1423-1427 10.1126/science.1207922
    • (2011) Science , vol.333 , pp. 1423-1427
    • Robbins, D.W.1    Hartwig, J.F.2
  • 5
    • 84890947807 scopus 로고    scopus 로고
    • Scientist-Led High-Throughput Experimentation (HTE) and Its Utility in Academia and Industry
    • Schmink, J. R.; Bellomo, A.; Berritt, S. Scientist-Led High-Throughput Experimentation (HTE) and Its Utility in Academia and Industry Aldrichimica Acta 2013, 46, 71-80
    • (2013) Aldrichimica Acta , vol.46 , pp. 71-80
    • Schmink, J.R.1    Bellomo, A.2    Berritt, S.3
  • 6
    • 84888809801 scopus 로고    scopus 로고
    • Cobalt Precursors for High-Throughput Discovery of Base Metal Asymmetric Alkene Hydrogenation Catalysts
    • Friedfeld, M. R.; Shevlin, M.; Hoyt, J. M.; Krska, S. W.; Tudge, M. T.; Chirik, P. J. Cobalt Precursors for High-Throughput Discovery of Base Metal Asymmetric Alkene Hydrogenation Catalysts Science 2013, 342, 1076-1080 10.1126/science.1243550
    • (2013) Science , vol.342 , pp. 1076-1080
    • Friedfeld, M.R.1    Shevlin, M.2    Hoyt, J.M.3    Krska, S.W.4    Tudge, M.T.5    Chirik, P.J.6
  • 7
    • 84920927241 scopus 로고    scopus 로고
    • Contemporary screening approaches to reaction discovery and development
    • Collins, K. D.; Gensch, T.; Glorius, F. Contemporary screening approaches to reaction discovery and development Nat. Chem. 2014, 6, 859-871 10.1038/nchem.2062
    • (2014) Nat. Chem. , vol.6 , pp. 859-871
    • Collins, K.D.1    Gensch, T.2    Glorius, F.3
  • 10
    • 0001087427 scopus 로고
    • Electronic Tuning of Asymmetric Catalysts
    • Jacobsen, E. N.; Zhang, W.; Guler, M. L. Electronic Tuning of Asymmetric Catalysts J. Am. Chem. Soc. 1991, 113, 6703-6704 10.1021/ja00017a069
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6703-6704
    • Jacobsen, E.N.1    Zhang, W.2    Guler, M.L.3
  • 11
    • 84868132395 scopus 로고    scopus 로고
    • New Applications of Isotope Effects in the Determination of Organic Reaction Mechanisms
    • Meyer, M. P. New Applications of Isotope Effects in the Determination of Organic Reaction Mechanisms Adv. Phys. Org. Chem. 2012, 46, 57-120 10.1016/B978-0-12-398484-5.00002-X
    • (2012) Adv. Phys. Org. Chem. , vol.46 , pp. 57-120
    • Meyer, M.P.1
  • 12
    • 84941244012 scopus 로고    scopus 로고
    • Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights
    • Sperger, T.; Sanhueza, I. A.; Kalvet, I.; Schoenebeck, F. Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights Chem. Rev. 2015, 115, 9532-86 10.1021/acs.chemrev.5b00163
    • (2015) Chem. Rev. , vol.115 , pp. 9532-9586
    • Sperger, T.1    Sanhueza, I.A.2    Kalvet, I.3    Schoenebeck, F.4
  • 13
    • 84925446149 scopus 로고    scopus 로고
    • Function through Synthesis-Informed Design
    • Wender, P. A.; Quiroz, R. V.; Stevens, M. C. Function through Synthesis-Informed Design Acc. Chem. Res. 2015, 48, 752-760 10.1021/acs.accounts.5b00004
    • (2015) Acc. Chem. Res. , vol.48 , pp. 752-760
    • Wender, P.A.1    Quiroz, R.V.2    Stevens, M.C.3
  • 14
    • 84925781492 scopus 로고    scopus 로고
    • A case study of the mechanism of alcohol-mediated Morita Baylis-Hillman reactions. The importance of experimental observations
    • Plata, R. E.; Singleton, D. A. A case study of the mechanism of alcohol-mediated Morita Baylis-Hillman reactions. The importance of experimental observations J. Am. Chem. Soc. 2015, 137, 3811-3826 10.1021/ja5111392
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 3811-3826
    • Plata, R.E.1    Singleton, D.A.2
  • 15
    • 84963563008 scopus 로고    scopus 로고
    • Electrostatic Basis for Enantioselective Brønsted-Acid Catalyzed Asymmetric Ring Openings of meso-Epoxides
    • Seguin, T. J.; Wheeler, S. E. Electrostatic Basis for Enantioselective Brønsted-Acid Catalyzed Asymmetric Ring Openings of meso-Epoxides ACS Catal. 2016, 6, 2681-2688 10.1021/acscatal.6b00538
    • (2016) ACS Catal. , vol.6 , pp. 2681-2688
    • Seguin, T.J.1    Wheeler, S.E.2
  • 16
    • 84966267454 scopus 로고    scopus 로고
    • Computational Catalysis Using the Artificial Force Induced Reaction Method
    • Sameera, W. M.; Maeda, S.; Morokuma, K. Computational Catalysis Using the Artificial Force Induced Reaction Method Acc. Chem. Res. 2016, 49, 763-773 10.1021/acs.accounts.6b00023
    • (2016) Acc. Chem. Res. , vol.49 , pp. 763-773
    • Sameera, W.M.1    Maeda, S.2    Morokuma, K.3
  • 17
    • 84966351248 scopus 로고    scopus 로고
    • Theory and Modeling of Asymmetric Catalytic Reactions
    • Lam, Y. H.; Grayson, M. N.; Holland, M. C.; Simon, A.; Houk, K. N. Theory and Modeling of Asymmetric Catalytic Reactions Acc. Chem. Res. 2016, 49, 750-62 10.1021/acs.accounts.6b00006
    • (2016) Acc. Chem. Res. , vol.49 , pp. 750-762
    • Lam, Y.H.1    Grayson, M.N.2    Holland, M.C.3    Simon, A.4    Houk, K.N.5
  • 18
    • 84963522319 scopus 로고    scopus 로고
    • Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link
    • Thomas, A. A.; Denmark, S. E. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link Science 2016, 352, 329-332 10.1126/science.aad6981
    • (2016) Science , vol.352 , pp. 329-332
    • Thomas, A.A.1    Denmark, S.E.2
  • 19
    • 33645532122 scopus 로고    scopus 로고
    • Ligand-Modulated Palladium-Catalyzed Aerobic Alcohol Oxidations
    • Sigman, M. S.; Jensen, D. R. Ligand-Modulated Palladium-Catalyzed Aerobic Alcohol Oxidations Acc. Chem. Res. 2006, 39, 221-229 10.1021/ar040243m
    • (2006) Acc. Chem. Res. , vol.39 , pp. 221-229
    • Sigman, M.S.1    Jensen, D.R.2
  • 20
    • 34347212512 scopus 로고    scopus 로고
    • Systematically Probing the Effect of Catalyst Acidity in a Hydrogen-Bond-Catalyzed Enantioselective Reaction
    • Jensen, K. H.; Sigman, M. S. Systematically Probing the Effect of Catalyst Acidity in a Hydrogen-Bond-Catalyzed Enantioselective Reaction Angew. Chem., Int. Ed. 2007, 46, 4748-4750 10.1002/anie.200700298
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4748-4750
    • Jensen, K.H.1    Sigman, M.S.2
  • 21
    • 78650113123 scopus 로고    scopus 로고
    • Advancing the Mechanistic Understanding of an Enantioselective Palladium-Catalyzed Alkene Difunctionalization Reaction
    • Jensen, K. H.; Webb, J. D.; Sigman, M. S. Advancing the Mechanistic Understanding of an Enantioselective Palladium-Catalyzed Alkene Difunctionalization Reaction J. Am. Chem. Soc. 2010, 132, 17471-17482 10.1021/ja108106h
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 17471-17482
    • Jensen, K.H.1    Webb, J.D.2    Sigman, M.S.3
  • 22
    • 78049487824 scopus 로고    scopus 로고
    • Evaluation of Catalyst Acidity and Substrate Electronic Effects in a Hydrogen Bond-Catalyzed Enantioselective Reaction
    • Jensen, K. H.; Sigman, M. S. Evaluation of Catalyst Acidity and Substrate Electronic Effects in a Hydrogen Bond-Catalyzed Enantioselective Reaction J. Org. Chem. 2010, 75, 7194-7201 10.1021/jo1013806
    • (2010) J. Org. Chem. , vol.75 , pp. 7194-7201
    • Jensen, K.H.1    Sigman, M.S.2
  • 23
    • 84863477460 scopus 로고    scopus 로고
    • Imparting Catalyst Control upon Classical Palladium-Catalyzed Alkenyl C-H Bond Functionalization Reactions
    • Sigman, M. S.; Werner, E. W. Imparting Catalyst Control upon Classical Palladium-Catalyzed Alkenyl C-H Bond Functionalization Reactions Acc. Chem. Res. 2012, 45, 874-884 10.1021/ar200236v
    • (2012) Acc. Chem. Res. , vol.45 , pp. 874-884
    • Sigman, M.S.1    Werner, E.W.2
  • 24
    • 38349070832 scopus 로고    scopus 로고
    • Quantitatively correlating the effect of ligand-substituent size in asymmetric catalysis using linear free energy relationships
    • Miller, J. J.; Sigman, M. S. Quantitatively correlating the effect of ligand-substituent size in asymmetric catalysis using linear free energy relationships Angew. Chem., Int. Ed. 2008, 47, 771-774 10.1002/anie.200704257
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 771-774
    • Miller, J.J.1    Sigman, M.S.2
  • 25
    • 84860234624 scopus 로고    scopus 로고
    • Multidimensional steric parameters in the analysis of asymmetric catalytic reactions
    • Harper, K. C.; Bess, E. N.; Sigman, M. S. Multidimensional steric parameters in the analysis of asymmetric catalytic reactions Nat. Chem. 2012, 4, 366-374 10.1038/nchem.1297
    • (2012) Nat. Chem. , vol.4 , pp. 366-374
    • Harper, K.C.1    Bess, E.N.2    Sigman, M.S.3
  • 26
    • 0000315307 scopus 로고
    • Steric effects. I. Esterification and acid-catalyzed hydrolysis of esters
    • Charton, M. Steric effects. I. Esterification and acid-catalyzed hydrolysis of esters J. Am. Chem. Soc. 1975, 97, 1552-1556 10.1021/ja00839a047
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1552-1556
    • Charton, M.1
  • 27
    • 70349871081 scopus 로고    scopus 로고
    • Examination of the Role of Taft-Type Steric Parameters in Asymmetric Catalysis
    • Sigman, M. S.; Miller, J. J. Examination of the Role of Taft-Type Steric Parameters in Asymmetric Catalysis J. Org. Chem. 2009, 74, 7633-7643 10.1021/jo901698t
    • (2009) J. Org. Chem. , vol.74 , pp. 7633-7643
    • Sigman, M.S.1    Miller, J.J.2
  • 28
    • 0000646292 scopus 로고
    • Nonlinear Hammett Relationships
    • Schreck, J. O. Nonlinear Hammett Relationships J. Chem. Educ. 1971, 48, 103 10.1021/ed048p103
    • (1971) J. Chem. Educ. , vol.48 , pp. 103
    • Schreck, J.O.1
  • 29
    • 0542443644 scopus 로고
    • A Reexamination of the Hammett Equation
    • Jaffé, H. H. A Reexamination of the Hammett Equation Chem. Rev. 1953, 53, 191-261 10.1021/cr60165a003
    • (1953) Chem. Rev. , vol.53 , pp. 191-261
    • Jaffé, H.H.1
  • 30
    • 0000255653 scopus 로고
    • A Simple Relationship between Carbocation Lifetime and Reactivity Selectivity Relationships for the Solvolysis of Ring-Substituted 1-Phenylethyl Derivatives
    • Richard, J. P.; Jencks, W. P. A Simple Relationship between Carbocation Lifetime and Reactivity Selectivity Relationships for the Solvolysis of Ring-Substituted 1-Phenylethyl Derivatives J. Am. Chem. Soc. 1982, 104, 4689-4691 10.1021/ja00381a037
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4689-4691
    • Richard, J.P.1    Jencks, W.P.2
  • 31
    • 79952284571 scopus 로고    scopus 로고
    • Predicting and optimizing asymmetric catalyst performance using the principles of experimental design and steric parameters
    • Harper, K. C.; Sigman, M. S. Predicting and optimizing asymmetric catalyst performance using the principles of experimental design and steric parameters Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 2179-2183 10.1073/pnas.1013331108
    • (2011) Proc. Natl. Acad. Sci. U. S. A. , vol.108 , pp. 2179-2183
    • Harper, K.C.1    Sigman, M.S.2
  • 33
    • 0038318801 scopus 로고    scopus 로고
    • Quantum Mechanical Models Correlating Structure with Selectivity: Predicting the Enantioselectivity of β-Amino Alcohol Catalysts in Aldehyde Alkylation
    • Kozlowski, M. C.; Dixon, S. L.; Panda, M.; Lauri, G. Quantum Mechanical Models Correlating Structure with Selectivity: Predicting the Enantioselectivity of β-Amino Alcohol Catalysts in Aldehyde Alkylation J. Am. Chem. Soc. 2003, 125, 6614-6615 10.1021/ja0293195
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6614-6615
    • Kozlowski, M.C.1    Dixon, S.L.2    Panda, M.3    Lauri, G.4
  • 34
    • 62849094142 scopus 로고    scopus 로고
    • Prediction of Enantioselectivity in Rhodium Catalyzed Hydrogenations
    • Donoghue, P. J.; Helquist, P.; Norrby, P.-O.; Wiest, O. Prediction of Enantioselectivity in Rhodium Catalyzed Hydrogenations J. Am. Chem. Soc. 2009, 131, 410-411 10.1021/ja806246h
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 410-411
    • Donoghue, P.J.1    Helquist, P.2    Norrby, P.-O.3    Wiest, O.4
  • 35
    • 79957823592 scopus 로고    scopus 로고
    • A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Application of quantitative structure activity/selectivity relationships
    • Denmark, S. E.; Gould, N. D.; Wolf, L. M. A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Application of quantitative structure activity/selectivity relationships J. Org. Chem. 2011, 76, 4337-4357 10.1021/jo2005457
    • (2011) J. Org. Chem. , vol.76 , pp. 4337-4357
    • Denmark, S.E.1    Gould, N.D.2    Wolf, L.M.3
  • 36
    • 84947785951 scopus 로고    scopus 로고
    • Design of Experiments (DoE) and Process Optimization. A Review of Recent Publications
    • Weissman, S. A.; Anderson, N. G. Design of Experiments (DoE) and Process Optimization. A Review of Recent Publications Org. Process Res. Dev. 2015, 19, 1605-1633 10.1021/op500169m
    • (2015) Org. Process Res. Dev. , vol.19 , pp. 1605-1633
    • Weissman, S.A.1    Anderson, N.G.2
  • 37
    • 80053343818 scopus 로고    scopus 로고
    • Three-Dimensional Correlation of Steric and Electronic Free Energy Relationships Guides Asymmetric Propargylation
    • Harper, K. C.; Sigman, M. S. Three-Dimensional Correlation of Steric and Electronic Free Energy Relationships Guides Asymmetric Propargylation Science 2011, 333, 1875-1878 10.1126/science.1206997
    • (2011) Science , vol.333 , pp. 1875-1878
    • Harper, K.C.1    Sigman, M.S.2
  • 38
    • 84871083602 scopus 로고    scopus 로고
    • Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy
    • Werner, E. W.; Mei, T.-S.; Burckle, A. J.; Sigman, M. S. Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy Science 2012, 338, 1455-1458 10.1126/science.1229208
    • (2012) Science , vol.338 , pp. 1455-1458
    • Werner, E.W.1    Mei, T.-S.2    Burckle, A.J.3    Sigman, M.S.4
  • 40
    • 77953581294 scopus 로고    scopus 로고
    • Linear Free-Energy Relationship Analysis of a Catalytic Desymmetrization Reaction of a Diarylmethane-bis(phenol)
    • Gustafson, J. L.; Sigman, M. S.; Miller, S. J. Linear Free-Energy Relationship Analysis of a Catalytic Desymmetrization Reaction of a Diarylmethane-bis(phenol) Org. Lett. 2010, 12, 2794-2797 10.1021/ol100927m
    • (2010) Org. Lett. , vol.12 , pp. 2794-2797
    • Gustafson, J.L.1    Sigman, M.S.2    Miller, S.J.3
  • 41
    • 0013143756 scopus 로고
    • A comparative study of new steric parameters in drug design
    • Verloop, A.; Tipker, J. A comparative study of new steric parameters in drug design Pharmacochem. Libr. 1977, 2, 63-81
    • (1977) Pharmacochem. Libr. , vol.2 , pp. 63-81
    • Verloop, A.1    Tipker, J.2
  • 42
    • 1842332527 scopus 로고
    • Electrophilic Substituent Constants
    • Brown, H. C.; Okamoto, Y. Electrophilic Substituent Constants J. Am. Chem. Soc. 1958, 80, 4979-4987 10.1021/ja01551a055
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 4979-4987
    • Brown, H.C.1    Okamoto, Y.2
  • 43
    • 0001364711 scopus 로고
    • The Infrared Carbonyl Stretching Bands of Ring Substituted Acetophenones
    • Jones, R. N.; Forbes, W. F.; Mueller, W. A. The Infrared Carbonyl Stretching Bands of Ring Substituted Acetophenones Can. J. Chem. 1957, 35, 504-514 10.1139/v57-071
    • (1957) Can. J. Chem. , vol.35 , pp. 504-514
    • Jones, R.N.1    Forbes, W.F.2    Mueller, W.A.3
  • 44
    • 84896291895 scopus 로고    scopus 로고
    • Interrogating selectivity in catalysis using molecular vibrations
    • Milo, A.; Bess, E. N.; Sigman, M. S. Interrogating selectivity in catalysis using molecular vibrations Nature 2014, 507, 210-214 10.1038/nature13019
    • (2014) Nature , vol.507 , pp. 210-214
    • Milo, A.1    Bess, E.N.2    Sigman, M.S.3
  • 45
    • 84874060886 scopus 로고    scopus 로고
    • Prediction of Catalyst and Substrate Performance in the Enantioselective Propargylation of Aliphatic Ketones by a Multidimensional Model of Steric Effects
    • Harper, K. C.; Vilardi, S. C.; Sigman, M. S. Prediction of Catalyst and Substrate Performance in the Enantioselective Propargylation of Aliphatic Ketones by a Multidimensional Model of Steric Effects J. Am. Chem. Soc. 2013, 135, 2482-2485 10.1021/ja4001807
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 2482-2485
    • Harper, K.C.1    Vilardi, S.C.2    Sigman, M.S.3
  • 46
    • 84907942360 scopus 로고    scopus 로고
    • Designer substrate library for quantitative, predictive modeling of reaction performance
    • Bess, E. N.; Bischoff, A. J.; Sigman, M. S. Designer substrate library for quantitative, predictive modeling of reaction performance Proc. Natl. Acad. Sci. U. S. A. 2014, 111, 14698-14703 10.1073/pnas.1409522111
    • (2014) Proc. Natl. Acad. Sci. U. S. A. , vol.111 , pp. 14698-14703
    • Bess, E.N.1    Bischoff, A.J.2    Sigman, M.S.3
  • 48
    • 0033515561 scopus 로고    scopus 로고
    • New Chiral Rhodium and Iridium Complexes with Chiral Diamine Ligands for Asymmetric Transfer Hydrogenation of Aromatic Ketones
    • Murata, K.; Ikariya, T.; Noyori, R. New Chiral Rhodium and Iridium Complexes with Chiral Diamine Ligands for Asymmetric Transfer Hydrogenation of Aromatic Ketones J. Org. Chem. 1999, 64, 2186-2187 10.1021/jo990213a
    • (1999) J. Org. Chem. , vol.64 , pp. 2186-2187
    • Murata, K.1    Ikariya, T.2    Noyori, R.3
  • 49
    • 34250201122 scopus 로고    scopus 로고
    • Aqueous-Phase Asymmetric Transfer Hydrogenation of Ketones - A Greener Approach to Chiral Alcohols
    • Wu, X.; Xiao, J. Aqueous-Phase Asymmetric Transfer Hydrogenation of Ketones-A Greener Approach to Chiral Alcohols Chem. Commun. 2007, 2449-2466 10.1039/b618340a
    • (2007) Chem. Commun. , pp. 2449-2466
    • Wu, X.1    Xiao, J.2
  • 50
    • 0035800369 scopus 로고    scopus 로고
    • CH/φ Attraction: The Origin of Enantioselectivity in Transfer Hydrogenation of Aromatic Carbonyl Compounds Catalyzed by Chiral n6-Arene-Ruthenium(II) Complexes
    • Yamakawa, M.; Yamada, I.; Noyori, R. CH/φ Attraction: The Origin of Enantioselectivity in Transfer Hydrogenation of Aromatic Carbonyl Compounds Catalyzed by Chiral n6-Arene-Ruthenium(II) Complexes Angew. Chem., Int. Ed. 2001, 40, 2818-2821 10.1002/1521-3773(20010803)40:15<2818::AID-ANIE2818>3.0.CO;2-Y
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2818-2821
    • Yamakawa, M.1    Yamada, I.2    Noyori, R.3
  • 51
    • 84953432210 scopus 로고    scopus 로고
    • Predicting Electrocatalytic Properties: Modeling Structure-Activity Relationships of Nitroxyl Radicals
    • Hickey, D. P.; Schiedler, D. A.; Matanovic, I.; Doan, P. V.; Atanassov, P.; Minteer, S. D.; Sigman, M. S. Predicting Electrocatalytic Properties: Modeling Structure-Activity Relationships of Nitroxyl Radicals J. Am. Chem. Soc. 2015, 137, 16179-16186 10.1021/jacs.5b11252
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 16179-16186
    • Hickey, D.P.1    Schiedler, D.A.2    Matanovic, I.3    Doan, P.V.4    Atanassov, P.5    Minteer, S.D.6    Sigman, M.S.7
  • 52
    • 84971367775 scopus 로고    scopus 로고
    • Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes
    • Niemeyer, Z. L.; Milo, A.; Hickey, D. P.; Sigman, M. S. Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes Nat. Chem. 2016, 10.1038/nchem.2501
    • (2016) Nat. Chem.
    • Niemeyer, Z.L.1    Milo, A.2    Hickey, D.P.3    Sigman, M.S.4
  • 53
    • 84923079453 scopus 로고    scopus 로고
    • A Data-Intensive Approach to Mechanistic Elucidation Applied to Chiral Anion Catalysis
    • Milo, A.; Neel, A. J.; Toste, F. D.; Sigman, M. S. A Data-Intensive Approach to Mechanistic Elucidation Applied to Chiral Anion Catalysis Science 2015, 347, 737-743 10.1126/science.1261043
    • (2015) Science , vol.347 , pp. 737-743
    • Milo, A.1    Neel, A.J.2    Toste, F.D.3    Sigman, M.S.4
  • 54
    • 84918774922 scopus 로고    scopus 로고
    • An in Situ Directing Group Strategy for Chiral Anion Phase-Transfer Fluorination of Allylic Alcohols
    • Zi, W.; Wang, Y.-M.; Toste, F. D. An In Situ Directing Group Strategy for Chiral Anion Phase-Transfer Fluorination of Allylic Alcohols J. Am. Chem. Soc. 2014, 136, 12864-12867 10.1021/ja507468u
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 12864-12867
    • Zi, W.1    Wang, Y.-M.2    Toste, F.D.3
  • 55
    • 84962045450 scopus 로고    scopus 로고
    • Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion
    • Neel, A. J.; Milo, A.; Sigman, M. S.; Toste, F. D. Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion J. Am. Chem. Soc. 2016, 138, 3863-3875 10.1021/jacs.6b00356
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 3863-3875
    • Neel, A.J.1    Milo, A.2    Sigman, M.S.3    Toste, F.D.4
  • 57
    • 84928152729 scopus 로고    scopus 로고
    • Using IR vibrations to quantitatively describe and predict site-selectivity in multivariate Rh-catalyzed C-H functionalization
    • Bess, E. N.; Guptill, D. M.; Davies, H. M. L.; Sigman, M. S. Using IR vibrations to quantitatively describe and predict site-selectivity in multivariate Rh-catalyzed C-H functionalization Chem. Sci. 2015, 6, 3057-3062 10.1039/C5SC00357A
    • (2015) Chem. Sci. , vol.6 , pp. 3057-3062
    • Bess, E.N.1    Guptill, D.M.2    Davies, H.M.L.3    Sigman, M.S.4
  • 58
    • 84930226503 scopus 로고    scopus 로고
    • Quantitatively Analyzing Metathesis Catalyst Activity and Structural Features in Silica-Supported Tungsten Imido-Alkylidene Complexes
    • Mougel, V.; Santiago, C. B.; Zhizhko, P. A.; Bess, E. N.; Varga, J.; Frater, G.; Sigman, M. S.; Copéret, C. Quantitatively Analyzing Metathesis Catalyst Activity and Structural Features in Silica-Supported Tungsten Imido-Alkylidene Complexes J. Am. Chem. Soc. 2015, 137, 6699-6704 10.1021/jacs.5b03344
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 6699-6704
    • Mougel, V.1    Santiago, C.B.2    Zhizhko, P.A.3    Bess, E.N.4    Varga, J.5    Frater, G.6    Sigman, M.S.7    Copéret, C.8
  • 59
    • 84952802828 scopus 로고    scopus 로고
    • Enantioselective Dehydrogenative Heck Arylations of Trisubstituted Alkenes with Indoles to Construct Quaternary Stereocenters
    • Zhang, C.; Santiago, C. B.; Crawford, J. M.; Sigman, M. S. Enantioselective Dehydrogenative Heck Arylations of Trisubstituted Alkenes with Indoles to Construct Quaternary Stereocenters J. Am. Chem. Soc. 2015, 137, 15668-15671 10.1021/jacs.5b11335
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 15668-15671
    • Zhang, C.1    Santiago, C.B.2    Crawford, J.M.3    Sigman, M.S.4
  • 60
    • 84935031979 scopus 로고    scopus 로고
    • Alkenyl Carbonyl Derivatives in Enantioselective Redox Relay Heck Reactions: Accessing α,β-Unsaturated Systems
    • Zhang, C.; Santiago, C. B.; Kou, L.; Sigman, M. S. Alkenyl Carbonyl Derivatives in Enantioselective Redox Relay Heck Reactions: Accessing α,β-Unsaturated Systems J. Am. Chem. Soc. 2015, 137, 7290-7293 10.1021/jacs.5b04289
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 7290-7293
    • Zhang, C.1    Santiago, C.B.2    Kou, L.3    Sigman, M.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.