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Volumn 118, Issue 14, 2014, Pages 2638-2645

Reactivity for the Diels-Alder reaction of cumulenes: A distortion-interaction analysis along the reaction pathway

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; OLEFINS;

EID: 84898466316     PISSN: 10895639     EISSN: 15205215     Source Type: Journal    
DOI: 10.1021/jp411914u     Document Type: Article
Times cited : (86)

References (95)
  • 1
    • 4143054706 scopus 로고
    • Potential Energy Surfaces for Polyatomic Reaction Dynamics
    • Truhlar, D. G.; Steckler, R.; Gordon, M. S. Potential Energy Surfaces for Polyatomic Reaction Dynamics Chem. Rev. 1987, 87, 217-236
    • (1987) Chem. Rev. , vol.87 , pp. 217-236
    • Truhlar, D.G.1    Steckler, R.2    Gordon, M.S.3
  • 2
    • 0000677365 scopus 로고
    • The Analytical Representation of Electronic Potential-Energy Surfaces
    • Schatz, G. C the Analytical Representation of Electronic Potential-Energy Surfaces Rev. Mod. Phys. 1989, 61, 669-688
    • (1989) Rev. Mod. Phys. , vol.61 , pp. 669-688
    • Schatz, G.C.1
  • 3
    • 0000211409 scopus 로고
    • Transition State Theory
    • Pechukas, P. Transition State Theory Annu. Rev. Phys. Chem. 1981, 32, 159-177
    • (1981) Annu. Rev. Phys. Chem. , vol.32 , pp. 159-177
    • Pechukas, P.1
  • 4
    • 0347657700 scopus 로고
    • The Equilibrium Statistical Mechanics of Simple Quasi-Geostrophic models
    • Salmon, R.; Holloway, G.; Hendershott, M. C the Equilibrium Statistical Mechanics of Simple Quasi-Geostrophic models J. Fluid Mech. 1976, 75, 691-703
    • (1976) J. Fluid Mech. , vol.75 , pp. 691-703
    • Salmon, R.1    Holloway, G.2    Hendershott, M.C.3
  • 5
    • 0000823158 scopus 로고
    • Equilibrium Statistical Mechanics of Matter Interacting with the Quantized Raljiation Field
    • Hepp, K.; Lieb, E. H. Equilibrium Statistical Mechanics of Matter Interacting with the Quantized Raljiation Field Phys. Rev. A 1973, 8, 2517-2525
    • (1973) Phys. Rev. A , vol.8 , pp. 2517-2525
    • Hepp, K.1    Lieb, E.H.2
  • 6
    • 37049150103 scopus 로고
    • Theoretical Tyeatment of the Diels-Alder Reaction. Part I. Polycyclic Aromatic Hydrocarbons
    • Brown, R. D. A Theoretical Tyeatment of the Diels-Alder Reaction. Part I. Polycyclic Aromatic Hydrocarbons J. Chem. Soc. 1950, 691-697
    • (1950) J. Chem. Soc. , pp. 691-697
    • Brown, R.D.A.1
  • 7
    • 33847086434 scopus 로고
    • Diels-Alder Reactivity of Polycyclic Aromatic Hydrocarbons. 2. Phenes and Starphenes
    • Biermann, D.; Schmidt, W. Diels-Alder Reactivity of Polycyclic Aromatic Hydrocarbons. 2. Phenes and Starphenes J. Am. Chem. Soc. 1980, 102, 3173-3181
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 3173-3181
    • Biermann, D.1    Schmidt, W.2
  • 9
    • 33947293579 scopus 로고
    • Hückel Molecular Orbital π Resonance Energies. A New Approach
    • Hess, B. A., Jr.; Schaad, L. J. Hückel Molecular Orbital π Resonance Energies. A New Approach J. Am. Chem. Soc. 1971, 93, 305-310
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 305-310
    • Hess, Jr.B.A.1    Schaad, L.J.2
  • 10
    • 0039851314 scopus 로고
    • A Reactivity Criterion of Aromaticity and Antiaromaticity in Macrocyclic Annulenes
    • Wightman, R. H.; Cresp, T. M.; Sondheimer, F. A Reactivity Criterion of Aromaticity and Antiaromaticity in Macrocyclic Annulenes J. Am. Chem. Soc. 1976, 98, 6052-6053
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 6052-6053
    • Wightman, R.H.1    Cresp, T.M.2    Sondheimer, F.3
  • 11
    • 0346888810 scopus 로고
    • The Frontier Molecular Orbital Theory of Cycloaddition Reactions
    • Houk, K. N the Frontier Molecular Orbital Theory of Cycloaddition Reactions Acc. Chem. Res. 1975, 8, 361-369
    • (1975) Acc. Chem. Res. , vol.8 , pp. 361-369
    • Houk, K.N.1
  • 12
    • 0000780859 scopus 로고
    • Kinetics of 1, 3-dipolar Cycloaddition Reactions of Diazomethane; A Correlation with Homo-Lumo Energies
    • Geittner, J.; Huisgen, R.; Sustmann, R. Kinetics of 1, 3-dipolar Cycloaddition Reactions of Diazomethane; A Correlation with Homo-Lumo Energies Tetrahedron Lett. 1977, 10, 881-884
    • (1977) Tetrahedron Lett. , vol.10 , pp. 881-884
    • Geittner, J.1    Huisgen, R.2    Sustmann, R.3
  • 13
    • 33947321923 scopus 로고
    • Intermolecular Orbital Theory of the Interaction between Conjugated Systems. I. General Theory
    • Salem, L. Intermolecular Orbital Theory of the Interaction between Conjugated Systems. I. General Theory J. Am. Chem. Soc. 1968, 90, 543-552
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 543-552
    • Salem, L.1
  • 14
    • 33947301475 scopus 로고
    • Intermolecular Orbital Theory of the Interaction between Conjugated Systems. II thermal and Photochemical Cycloadditions
    • Salem, L. Intermolecular Orbital Theory of the Interaction between Conjugated Systems. II thermal and Photochemical Cycloadditions J. Am. Chem. Soc. 1968, 90, 553-566
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 553-566
    • Salem, L.1
  • 15
    • 0002313438 scopus 로고
    • Recognition of Stereochemical Paths by Orbital Interaction
    • Fukui, K. Recognition of Stereochemical Paths by Orbital Interaction Acc. Chem. Res. 1971, 4, 57-64
    • (1971) Acc. Chem. Res. , vol.4 , pp. 57-64
    • Fukui, K.1
  • 16
    • 36849118773 scopus 로고
    • On the Theory of Electron-Transfer Reactions. VI. Unified Treatment for Homogeneous and Electrode Reactions
    • Marcus, R. A. On the Theory of Electron-Transfer Reactions. VI. Unified Treatment for Homogeneous and Electrode Reactions J. Chem. Phys. 1965, 43, 679-701
    • (1965) J. Chem. Phys. , vol.43 , pp. 679-701
    • Marcus, R.A.1
  • 17
    • 3042520570 scopus 로고
    • A Primer for the Bema Hapothle. An Empirical Approach to the Characterization of Changing Transition-State Structures
    • Jencks, W. P. A Primer for the Bema Hapothle. An Empirical Approach to the Characterization of Changing Transition-State Structures Chem. Rev. 1985, 85, 511-527
    • (1985) Chem. Rev. , vol.85 , pp. 511-527
    • Jencks, W.P.1
  • 18
    • 0002295580 scopus 로고    scopus 로고
    • Electron transfer reactions in chemistry theory and experiment
    • Marcus, R. A. Electron Transfer Reactions in Chemistry theory and Experiment Pure. Appl. Chem. 1997, 69, 13-29 (Pubitemid 127482726)
    • (1997) Pure and Applied Chemistry , vol.69 , Issue.1 , pp. 13-29
    • Marcus, R.A.1
  • 19
    • 44849085727 scopus 로고    scopus 로고
    • Bell-Evans-Polanyi Principle for Molecular Dynamics Trajectories and Its Implications for Global Optimization
    • Roy, S.; Goedecker, S.; Hellmann, V. Bell-Evans-Polanyi Principle for Molecular Dynamics Trajectories and Its Implications for Global Optimization Phys. Rev. E 2008, 77, 056707-056711
    • (2008) Phys. Rev. e , vol.77 , pp. 056707-056711
    • Roy, S.1    Goedecker, S.2    Hellmann, V.3
  • 20
    • 0001516390 scopus 로고    scopus 로고
    • Prediction of approximate transition states by Bell-Evans-Polanyi principle: I
    • Anglada, J. M.; Besalú, E.; Bofill, J. M.; Crehuet, R. Prediction of Approximate Transition States by Bell-Evans-Polanyi Principle: I J. Comput. Chem. 1999, 20, 1112-1129 (Pubitemid 129651744)
    • (1999) Journal of Computational Chemistry , vol.20 , Issue.11 , pp. 1112-1129
    • Anglada, J.M.1    Besalu, E.2    Bofill, J.M.3    Crehuet, R.4
  • 21
    • 33846636504 scopus 로고    scopus 로고
    • Hydrogenation of simple aromatic molecules: A computational study of the mechanism
    • DOI 10.1021/ja066251a
    • Zhong, G.; Chan, B.; Radom, L. Hydrogenation of Simple Aromatic Molecules: A Computational Study of the Mechanism J. Am. Chem. Soc. 2007, 129, 924-933 (Pubitemid 46183942)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.4 , pp. 924-933
    • Zhong, G.1    Chan, B.2    Radom, L.3
  • 22
    • 0012900907 scopus 로고
    • An ab Initio Molecular Orbital Study of Organic Reactions the Energy, Charge, and Spin Decomposition Analyses at the Transition State and along the Reaction Pathway
    • Nagase, S.; Morokuma, K. An ab Initio Molecular Orbital Study of Organic Reactions the Energy, Charge, and Spin Decomposition Analyses at the Transition State and along the Reaction Pathway J. Am. Chem. Soc. 1978, 100, 1666-1672
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 1666-1672
    • Nagase, S.1    Morokuma, K.2
  • 23
    • 35948953157 scopus 로고    scopus 로고
    • Distortion/interaction energy control of 1,3-dipolar cycloaddition reactivity
    • DOI 10.1021/ja0734086
    • Ess, D. H.; Houk, K. N. Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity J. Am. Chem. Soc. 2007, 129, 10646-10647 (Pubitemid 350067461)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.35 , pp. 10646-10647
    • Ess, D.H.1    Houk, K.N.2
  • 24
    • 79960269088 scopus 로고    scopus 로고
    • Extraordinary Difference in Reactivity of Ozone (OOO) and Sulfur Dioxide (OSO): A Theoretical Study
    • Lan, Y.; Wheeler, S. E.; Houk, K. N. Extraordinary Difference in Reactivity of Ozone (OOO) and Sulfur Dioxide (OSO): A Theoretical Study J. Chem theory Comput. 2011, 7, 2104-2111
    • (2011) J. Chem theory Comput. , vol.7 , pp. 2104-2111
    • Lan, Y.1    Wheeler, S.E.2    Houk, K.N.3
  • 25
    • 64349103238 scopus 로고    scopus 로고
    • 4-Alkene (M = Os, Re, Tc, Mn) Cycloadditions
    • 4-Alkene (M = Os, Re, Tc, Mn) Cycloadditions J. Org. Chem. 2009, 74, 1498-1508
    • (2009) J. Org. Chem. , vol.74 , pp. 1498-1508
    • Ess, D.H.1
  • 26
    • 67749099629 scopus 로고    scopus 로고
    • Transition State Distortion Energies Correlate with Activation Energies of 1,4-Dihydrogenations and Diels-Alder Cycloadditions of Aromatic Molecules
    • Hayden, A. E.; Houk, K. N. Transition State Distortion Energies Correlate with Activation Energies of 1,4-Dihydrogenations and Diels-Alder Cycloadditions of Aromatic Molecules J. Am. Chem. Soc. 2009, 131, 4084-4089
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4084-4089
    • Hayden, A.E.1    Houk, K.N.2
  • 28
    • 0000418426 scopus 로고
    • Ketene Chemistry: The Second Golden Age
    • Tidwell, T. T. Ketene Chemistry: The Second Golden Age Acc. Chem. Res. 1990, 23, 273-279
    • (1990) Acc. Chem. Res. , vol.23 , pp. 273-279
    • Tidwell, T.T.1
  • 30
    • 0015980359 scopus 로고
    • Heterocumulene Molecular Orbitals: Ketenes, Isocyanates, Sulfenes, and Sulfonylanines
    • Houk, K. N.; Strozier, R. W.; Hall, J. A. Heterocumulene Molecular Orbitals: Ketenes, Isocyanates, Sulfenes, and Sulfonylanines Tetrahedron Lett. 1974, 15, 897-900
    • (1974) Tetrahedron Lett. , vol.15 , pp. 897-900
    • Houk, K.N.1    Strozier, R.W.2    Hall, J.A.3
  • 31
    • 0032542196 scopus 로고    scopus 로고
    • 1,3-asymmetric induction in the intramolecular [2+2] cycloaddition of alkene-keteniminium salts. Synthesis of (+)-gibberellic acid key intermediate
    • PII S004040399802228X
    • Shim, P.-J.; Kim, H.-D. 1,3-Asymmetric Induction in the Intramolecular [2 + 2] Cycloaddition of Alkene-keteniminium Salts. Synthesis of (+)-Gibberellic Acid Key Intermediate Tetrahedron Lett. 1998, 39, 9517-9520 (Pubitemid 28541120)
    • (1998) Tetrahedron Letters , vol.39 , Issue.51 , pp. 9517-9520
    • Shim, P.-J.1    Kim, H.-D.2
  • 32
  • 34
    • 33748495125 scopus 로고    scopus 로고
    • Synthesis of β-lactams from fluoroketenes and imines: Ab initio potential energy surfaces in gas phase and in solution
    • López, R.; Ruiz-López, M. F.; Rinaldi, D.; Sordo, J. A.; Sordo, T. L. Synthesis of β-Lactams from Fluoroketenes and Imines: Ab Initio Potential Energy Surfaces in Gas Phase and in Solution J. Phys. Chem. 1996, 100, 10600-10608 (Pubitemid 126788648)
    • (1996) Journal of Physical Chemistry , vol.100 , Issue.25 , pp. 10600-10608
    • Lopez, R.1    Ruiz-Lopez, M.F.2    Rinaldi, D.3    Sordo, J.A.4    Sordo, T.L.5
  • 35
    • 2142684887 scopus 로고    scopus 로고
    • Ab initio studies on the mechanism of the fluoroketene-imine cycloaddition reaction: Via a gauche or trans intermediate
    • Fang, D.-C.; Fu, X.-Y. Ab Initio Studies on the Mechanism of the Fluoroketene-Imine Cycloaddition Reaction: Via a gauche or trans Intermediate Int. J. Quantum Chem. 1996, 57, 1107-1114 (Pubitemid 126519871)
    • (1996) International Journal of Quantum Chemistry , vol.57 , Issue.6 , pp. 1107-1114
    • Fang, D.-C.1    Fu, X.-Y.2
  • 36
    • 0030907859 scopus 로고    scopus 로고
    • Peri-, site-, and regioselectivity in heterocumulene-heterodiene cycloaddition reactions: An ab initio study of the system ketenimine + acrolein
    • DOI 10.1021/ja963941d
    • Fabian, W. M. F.; Janoschek, R. Peri-, Site-, and Regioselectivity in Heterocumulene-Heterodiene Cycloaddition Reactions: An Ab Initio Study of the System Ketenimine + Acrolein J. Am. Chem. Soc. 1997, 119, 4253-4257 (Pubitemid 27239977)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.18 , pp. 4253-4257
    • Fabian, W.M.F.1    Janoschek, R.2
  • 37
    • 84990132418 scopus 로고
    • Cyclobutanones and Cyclobutenones in Nature and in Synthesis New Synthetic Methods
    • Belluš, D.; Ernst, B. Cyclobutanones and Cyclobutenones in Nature and in Synthesis New Synthetic Methods Angew. Chem., Int. Ed. Engl. 1988, 27, 797-827
    • (1988) Angew. Chem., Int. Ed. Engl. , vol.27 , pp. 797-827
    • Belluš, D.1    Ernst, B.2
  • 38
    • 84961978336 scopus 로고    scopus 로고
    • Theoretical studies on cycloaddition reactions between keteniminium cations and olefins
    • DOI 10.1021/jo010461i
    • Ding, W.-J.; Fang, D.-C theoretical Studies on Cycloaddition Reactions between Keteniminium Cations and Olefins J. Org. Chem. 2001, 66, 6673-6678 (Pubitemid 32946585)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.20 , pp. 6673-6678
    • Ding, W.-J.1    Fang, D.-C.2
  • 39
    • 75749105417 scopus 로고    scopus 로고
    • Diastereoselective Diels-Alder Reactions with an Allenyl-Containing Spiro-Amido Chiral Auxiliary
    • Henderson, J. R.; Chesterman, J. P.; Parvez, M.; Keay, B. A. Diastereoselective Diels-Alder Reactions with an Allenyl-Containing Spiro-Amido Chiral Auxiliary J. Org. Chem. 2010, 75, 988-991
    • (2010) J. Org. Chem. , vol.75 , pp. 988-991
    • Henderson, J.R.1    Chesterman, J.P.2    Parvez, M.3    Keay, B.A.4
  • 40
    • 33645210971 scopus 로고    scopus 로고
    • Synthesis of (-)-Epibatidine and Its Derivatives from Chiral Allene-1,3-dicarboxylate Esters
    • Kimura, H.; Fujiwara, T.; Katoh, T.; Nishide, K.; Kajimoto, T.; Node, M. Synthesis of (-)-Epibatidine and Its Derivatives from Chiral Allene-1,3-dicarboxylate Esters Chem. Pharm. Bull. 2006, 54, 399-402
    • (2006) Chem. Pharm. Bull. , vol.54 , pp. 399-402
    • Kimura, H.1    Fujiwara, T.2    Katoh, T.3    Nishide, K.4    Kajimoto, T.5    Node, M.6
  • 41
    • 33751423659 scopus 로고    scopus 로고
    • A practical improvement of crystallization-induced asymmetric transformation of allene-1,3-dicarboxylates
    • DOI 10.1016/j.tetasy.2006.11.004, PII S095741660600797X
    • Katoh, T.; Noguchi, C.; Kimura, H.; Fujiwara, T.; Ichihashi, S.; Nishide, K.; Kajimoto, T.; Node, M. A Practical Improvement of Crystallization-Induced Asymmetric Transformation of Allene-1,3-dicarboxylates Tetrahedron: Asymmetry 2006, 17, 2943-2951 (Pubitemid 44820840)
    • (2006) Tetrahedron Asymmetry , vol.17 , Issue.20 , pp. 2943-2951
    • Katoh, T.1    Noguchi, C.2    Kimura, H.3    Fujiwara, T.4    Ichihashi, S.5    Nishide, K.6    Kajimoto, T.7    Node, M.8
  • 42
    • 0032474789 scopus 로고    scopus 로고
    • Formal synthesis of natural epibatidine and of its enantiomer: Use of radical cyclization in an enantiospecific route
    • DOI 10.1016/S0040-4039(98)00958-7, PII S0040403998009587
    • Clive, D. L. J.; Yeh, V. S. C. Formal Synthesis of Natural Epibatidine and of its Enantiomer: Use of Radical Cyclization in an Enantiospecific Route Tetrahedron Lett. 1998, 39, 4789-4792 (Pubitemid 28267311)
    • (1998) Tetrahedron Letters , vol.39 , Issue.27 , pp. 4789-4792
    • Clive, D.L.J.1    Yeh, V.S.C.2
  • 43
    • 1542508435 scopus 로고
    • Asymmetric Diels-Alder Reaction of a Chiral Allenic Ester: Enantioselective Synthesis of (-)-β-Santalene
    • Oppolzer, W.; Chapuis, C. Asymmetric Diels-Alder Reaction of a Chiral Allenic Ester: Enantioselective Synthesis of (-)-β-Santalene Tetrahedron Lett. 1983, 24, 4665-4668
    • (1983) Tetrahedron Lett. , vol.24 , pp. 4665-4668
    • Oppolzer, W.1    Chapuis, C.2
  • 44
    • 84877802363 scopus 로고    scopus 로고
    • Studies on the Himbert Intramolecular Arene/Allene Diels-Alder Cycloaddition. Mechanistic Studies and Expansion of Scope to All-Carbon Tethers
    • Schmidt, Y.; Lam, J. K.; Pham, H. V.; Houk, K. N.; Vanderwal, C. D. Studies on the Himbert Intramolecular Arene/Allene Diels-Alder Cycloaddition. Mechanistic Studies and Expansion of Scope to All-Carbon Tethers J. Am. Chem. Soc. 2013, 135, 7339-7348
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 7339-7348
    • Schmidt, Y.1    Lam, J.K.2    Pham, H.V.3    Houk, K.N.4    Vanderwal, C.D.5
  • 45
    • 0033525196 scopus 로고    scopus 로고
    • Strained allenes as dienophiles in the Diels-Alder reaction: An experimental and computational study
    • DOI 10.1021/jo982091c
    • Nendel, M.; Tolbert, L. M.; Herring, L. E.; Islam, M. N.; Houk, K. N. Strained Allenes as Dienophiles in the Diels-Alder Reaction: An Experimental and Computational Study J. Org. Chem. 1999, 64, 976-983 (Pubitemid 29098026)
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.3 , pp. 976-983
    • Nendel, M.1    Tolbert, L.M.2    Herring, L.E.3    Islam, Md.N.4    Houk, K.N.5
  • 46
    • 84856466877 scopus 로고    scopus 로고
    • Entropic Intermediates and Hidden Rate-Limiting Steps in Seemingly Concerted Cycloadditions. Observation, Prediction, and Origin of an Isotope Effect on Recrossing
    • Gonzalez-James, O. M.; Kwan, E. E.; Singleton, D. A. Entropic Intermediates and Hidden Rate-Limiting Steps in Seemingly Concerted Cycloadditions. Observation, Prediction, and Origin of an Isotope Effect on Recrossing J. Am. Chem. Soc. 2012, 134, 1914-1917
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 1914-1917
    • Gonzalez-James, O.M.1    Kwan, E.E.2    Singleton, D.A.3
  • 47
    • 84857147091 scopus 로고    scopus 로고
    • New Directions in Ketene Chemistry: The Land of Opportunity
    • Allen, A. D.; Tidwell, T. T. New Directions in Ketene Chemistry: The Land of Opportunity Eur. J. Org. Chem. 2012, 1081-1096
    • (2012) Eur. J. Org. Chem. , pp. 1081-1096
    • Allen, A.D.1    Tidwell, T.T.2
  • 48
    • 67650694508 scopus 로고    scopus 로고
    • Catalytic, Asymmetric Reactions of Ketenes and Ketene Enolates
    • Paull, D. H.; Weatherwax, A.; Lectka, T. Catalytic, Asymmetric Reactions of Ketenes and Ketene Enolates Tetrahedron 2009, 65, 6771-6803
    • (2009) Tetrahedron , vol.65 , pp. 6771-6803
    • Paull, D.H.1    Weatherwax, A.2    Lectka, T.3
  • 49
    • 51649103509 scopus 로고    scopus 로고
    • The Mechanism of the Ketene-Imine (Staudinger) Reaction in Its Centennial: Still an Unsolved Problem?
    • Cossio, F. P.; Arrieta, A.; Sierra, M. A the Mechanism of the Ketene-Imine (Staudinger) Reaction in Its Centennial: Still an Unsolved Problem? Acc. Chem. Res. 2008, 41, 925-936
    • (2008) Acc. Chem. Res. , vol.41 , pp. 925-936
    • Cossio, F.P.1    Arrieta, A.2    Sierra, M.A.3
  • 50
    • 37049066718 scopus 로고
    • [4 + 2] Cycloadditions of Diphenylketene with a Highly Substituted 1,3-Diene
    • Mayr, H.; Heigl, U. W. [4 + 2] Cycloadditions of Diphenylketene with a Highly Substituted 1,3-Diene J. Chem. Soc., Chem. Commun. 1987, 1804-1805
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 1804-1805
    • Mayr, H.1    Heigl, U.W.2
  • 51
    • 23044469448 scopus 로고    scopus 로고
    • First [4 + 2] cycloadditions involving the olefinic bond of an 'aldoketeniminium salt' (= N-alk-1-enylideneaminium salt)
    • DOI 10.1002/hlca.200590154
    • Mahuteau-Betzer, F.; Ding, P.-Y.; Ghosez, L. First [4 + 2] Cycloadditions Involving the Olefinic Bond of an Aldoketeniminium Salt? (= N -Alk-1-enylideneaminium Salt) Helv. Chim. Acta 2005, 88, 2022-2031 (Pubitemid 41074560)
    • (2005) Helvetica Chimica Acta , vol.88 , Issue.7 , pp. 2022-2031
    • Mahuteau-Betzer, F.1    Ding, P.-Y.2    Ghosez, L.3
  • 52
    • 1542496403 scopus 로고
    • Intramolecular Cycloaddition Reactions of Ketenes and Keteniminium Salts with Alkenes
    • Snider, B. B. Intramolecular Cycloaddition Reactions of Ketenes and Keteniminium Salts with Alkenes Chem. Rev. 1988, 88, 793-811
    • (1988) Chem. Rev. , vol.88 , pp. 793-811
    • Snider, B.B.1
  • 53
    • 84860122325 scopus 로고    scopus 로고
    • The Diels-Alder Cyclization of Ketenimines
    • Erb, J.; Strull, J.; Miller, D.; He, J.; Lectka, T the Diels-Alder Cyclization of Ketenimines Org. Lett. 2012, 14, 2191-2193
    • (2012) Org. Lett. , vol.14 , pp. 2191-2193
    • Erb, J.1    Strull, J.2    Miller, D.3    He, J.4    Lectka, T.5
  • 55
    • 66449119101 scopus 로고    scopus 로고
    • [4 + 2] Cycloaddition Reaction of C -Aryl Ketenimines with PTAD as a Synthetic Equivalent of Dinitrogen. Synthesis of Triazolocinnolines and Cinnolines
    • Alajarin, M.; Bonillo, B.; Marin-Luna, M.; Vidal, A.; Orenes, R.-A. [4 + 2] Cycloaddition Reaction of C -Aryl Ketenimines with PTAD as a Synthetic Equivalent of Dinitrogen. Synthesis of Triazolocinnolines and Cinnolines J. Org. Chem. 2009, 74, 3558-3561
    • (2009) J. Org. Chem. , vol.74 , pp. 3558-3561
    • Alajarin, M.1    Bonillo, B.2    Marin-Luna, M.3    Vidal, A.4    Orenes, R.-A.5
  • 57
    • 33845280522 scopus 로고
    • Inverse Electron Demand Diels-Alder Reactions of 3,6-Bis(methylthio)-1,2, 4,5-tetrazine: 1,2-Diazine Introduction and Direct Implementation of a Divergent 1,2,4,5-Tetrazine → 1,2-Diazine → Benzene (Indoline/Indole) Diels-Alder Strategy
    • Boger, D. L.; Sakya, S. M. Inverse Electron Demand Diels-Alder Reactions of 3,6-Bis(methylthio)-1,2,4,5-tetrazine: 1,2-Diazine Introduction and Direct Implementation of a Divergent 1,2,4,5-Tetrazine → 1,2-Diazine → Benzene (Indoline/Indole) Diels-Alder Strategy J. Org. Chem. 1988, 53, 1415-1423
    • (1988) J. Org. Chem. , vol.53 , pp. 1415-1423
    • Boger, D.L.1    Sakya, S.M.2
  • 58
    • 0025871436 scopus 로고
    • Total Synthesis of (±)-cis- and (±)-trans-Trikentrin A: Diels-Alder Reactions of Heteroaromatic Azadienes
    • Boger, D. L.; Zhang, M. Total Synthesis of (±)-cis- and (±)-trans-Trikentrin A: Diels-Alder Reactions of Heteroaromatic Azadienes J. Am. Chem. Soc. 1991, 113, 4230-4234
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4230-4234
    • Boger, D.L.1    Zhang, M.2
  • 59
    • 84870531420 scopus 로고    scopus 로고
    • Tandem Inverse-Electron-Demand Hetero-/Retro-Diels-Alder Reactions for Aromatic Nitrogen Heterocycle Synthesis
    • Foster, R. A. A.; Willis, M. C. Tandem Inverse-Electron-Demand Hetero-/Retro-Diels-Alder Reactions for Aromatic Nitrogen Heterocycle Synthesis Chem. Soc. Rev. 2013, 42, 63-76
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 63-76
    • Foster, R.A.A.1    Willis, M.C.2
  • 61
    • 0001323102 scopus 로고
    • Ab Initio Studies on the Mechanism of the Cycloaddition Reaction of Fluoroketene with Imines: Substituent Effects
    • Xu, Z.-F.; Fang, D.-C.; Fu, X.-Y. Ab Initio Studies on the Mechanism of the Cycloaddition Reaction of Fluoroketene with Imines: Substituent Effects J. Mol. Struct. 1994, 305, 191-196
    • (1994) J. Mol. Struct. , vol.305 , pp. 191-196
    • Xu, Z.-F.1    Fang, D.-C.2    Fu, X.-Y.3
  • 62
    • 84990639723 scopus 로고
    • Ab Initio Study on the Mechanism of Cycloaddition Reaction of Ketene with Methylenimine: A New Reaction Scheme
    • Fang, D.; Fu, X. Ab Initio Study on the Mechanism of Cycloaddition Reaction of Ketene with Methylenimine: A New Reaction Scheme Int. J. Quantum Chem. 1992, 43, 669-676
    • (1992) Int. J. Quantum Chem. , vol.43 , pp. 669-676
    • Fang, D.1    Fu, X.2
  • 63
    • 70450206724 scopus 로고    scopus 로고
    • Revision A.02, Gaussian, Inc. Wallingford CT, The full author list is shown in Supporting Information
    • Frisch, M. J., Gaussian 09, Revision A.02, Gaussian, Inc., Wallingford CT, 2009 the full author list is shown in Supporting Information.
    • (2009) Gaussian 09
    • Frisch, M.J.1
  • 64
    • 4243553426 scopus 로고
    • Density-Functional Exchange-Energy Approximation with Correct Asymptotic Behavior
    • Becke, A. D. Density-Functional Exchange-Energy Approximation with Correct Asymptotic Behavior Phys. Rev. A 1988, 38, 3098-3100
    • (1988) Phys. Rev. A , vol.38 , pp. 3098-3100
    • Becke, A.D.1
  • 65
    • 0345491105 scopus 로고
    • Development of the Colic-Salvetti Correlation-Energy Formula into a Functional of the Electron Density
    • Lee, C.; Yang, W.; Parr, R. G. Development of the Colic-Salvetti Correlation-Energy Formula into a Functional of the Electron Density Phys. Rev. B 1988, 37, 785-789
    • (1988) Phys. Rev. B , vol.37 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, R.G.3
  • 66
    • 33751157732 scopus 로고
    • Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields
    • Stephens, P. J.; Devlin, F. J.; Chabalowski, C. F.; Frisch, M. J. Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields J. Phys. Chem. 1994, 98, 11623-11627
    • (1994) J. Phys. Chem. , vol.98 , pp. 11623-11627
    • Stephens, P.J.1    Devlin, F.J.2    Chabalowski, C.F.3    Frisch, M.J.4
  • 67
    • 0001475454 scopus 로고    scopus 로고
    • Toward Reliable Density Functional Methods without Adjustable Parameters: The PBE0 Model
    • Adamo, C.; Barone, V. Toward Reliable Density Functional Methods without Adjustable Parameters: The PBE0 Model J. Chem. Phys. 1999, 110, 6158-6170
    • (1999) J. Chem. Phys. , vol.110 , pp. 6158-6170
    • Adamo, C.1    Barone, V.2
  • 69
    • 27544455914 scopus 로고    scopus 로고
    • How well can density functional methods describe hydrogen bonds to π acceptors?
    • DOI 10.1021/jp0534434
    • Zhao, Y.; Tishchenko, O.; Truhlar, D. G. How Well Can Density Functional Methods Describe Hydrogen Bonds to π Acceptors? J. Phys. Chem. B 2005, 109, 19046-19051 (Pubitemid 41541098)
    • (2005) Journal of Physical Chemistry B , vol.109 , Issue.41 , pp. 19046-19051
    • Zhao, Y.1    Tishchenko, O.2    Truhlar, D.G.3
  • 70
    • 0035281210 scopus 로고    scopus 로고
    • Interaction energies of van der Waals and hydrogen bonded systems calculated using density functional theory: Assessing the PW91 model
    • DOI 10.1063/1.1344891
    • Tsuzuki, S.; Lüthi, H. P. Interaction Energies of Van Der Waals and Hydrogen Bonded Systems Calculated Using Density Functional Theory: Assessing the PW91 Model J. Chem. Phys. 2001, 114, 3949-3957 (Pubitemid 32255018)
    • (2001) Journal of Chemical Physics , vol.114 , Issue.9 , pp. 3949-3957
    • Tsuzuki, S.1    Luthi, H.P.2
  • 71
    • 17444384169 scopus 로고    scopus 로고
    • DFT calculations on the allenyl Cope rearrangement of syn-7-allenylnorbornene: Comparison with results obtained from CASSCF calculations
    • DOI 10.1002/poc.871
    • Duncan, J. A.; Spong, M. C. DFT Calculations on the Allenyl Cope Rearrangement of Syn -7-allenylnorbornene: Comparison with Results Obtained from CASSCF Calculations J. Phys. Org. Chem. 2005, 18, 462-467 (Pubitemid 40541338)
    • (2005) Journal of Physical Organic Chemistry , vol.18 , Issue.5 , pp. 462-467
    • Duncan, J.A.1    Spong, M.C.2
  • 72
    • 33748591851 scopus 로고    scopus 로고
    • Systematic errors in computed alkane energies using B3LYP and other popular DFT functionals
    • DOI 10.1021/ol061016i
    • Wodrich, M. D.; Corminboeuf, C.; Schleyer, P. V. R. Systematic Errors in Computed Alkane Energies Using B3LYP and Other Popular DFT Functionals Org. Lett. 2006, 8, 3631-3634 (Pubitemid 44378325)
    • (2006) Organic Letters , vol.8 , Issue.17 , pp. 3631-3634
    • Wodrich, M.D.1    Corminboeuf, C.2    Schleyer, P.V.R.3
  • 73
    • 43049141516 scopus 로고    scopus 로고
    • The M06 Suite of Density Functionals for Main Group Thermochemistry, Thermochemical Kinetics, Noncovalent Interactions, Excited States, and Transition Elements: Two New Functionals and Systematic Testing of Four M06-class Functionals and 12 Other Functionals
    • Zhao, Y.; Truhlar, D. G the M06 Suite of Density Functionals for Main Group Thermochemistry, Thermochemical Kinetics, Noncovalent Interactions, Excited States, and Transition Elements: Two New Functionals and Systematic Testing of Four M06-class Functionals and 12 Other Functionals Theor. Chem. Acc. 2008, 120, 215-241
    • (2008) Theor. Chem. Acc. , vol.120 , pp. 215-241
    • Zhao, Y.1    Truhlar, D.G.2
  • 74
    • 47149115671 scopus 로고    scopus 로고
    • Benchmark Data for Interactions in Zeolite Model Complexes and Their Use for Assessment and Validation of Electronic Structure Methods
    • Zhao, Y.; Truhlar, D. G. Benchmark Data for Interactions in Zeolite Model Complexes and Their Use for Assessment and Validation of Electronic Structure Methods J. Phys. Chem. C 2008, 112, 6860-6868
    • (2008) J. Phys. Chem. C , vol.112 , pp. 6860-6868
    • Zhao, Y.1    Truhlar, D.G.2
  • 75
    • 35548929060 scopus 로고    scopus 로고
    • Computing Reliable Energetics for Conjugate Addition Reactions
    • Rokob, T. A.; Hamza, A.; Pápai, I. Computing Reliable Energetics for Conjugate Addition Reactions Org. Lett. 2007, 9, 4279-4282
    • (2007) Org. Lett. , vol.9 , pp. 4279-4282
    • Rokob, T.A.1    Hamza, A.2    Pápai, I.3
  • 76
    • 77949389582 scopus 로고    scopus 로고
    • Probing Substituent Effects in Aryl-Aryl Interactions Using Stereoselective Diels-Alder Cycloadditions
    • Wheeler, S. E.; McNeil, A. J.; Müller, P.; Swager, T. M.; Houk, K. N. Probing Substituent Effects in Aryl-Aryl Interactions Using Stereoselective Diels-Alder Cycloadditions J. Am. Chem. Soc. 2010, 132, 3304-3311
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 3304-3311
    • Wheeler, S.E.1    McNeil, A.J.2    Müller, P.3    Swager, T.M.4    Houk, K.N.5
  • 77
    • 77949347282 scopus 로고    scopus 로고
    • Integration Grid Errors for Meta-GGA-Predicted Reaction Energies: Origin of Grid Errors for the M06 Suite of Functionals
    • Wheeler, S. E.; Houk, K. N. Integration Grid Errors for Meta-GGA-Predicted Reaction Energies: Origin of Grid Errors for the M06 Suite of Functionals J. Chem theory Comput. 2010, 6, 395-404
    • (2010) J. Chem theory Comput. , vol.6 , pp. 395-404
    • Wheeler, S.E.1    Houk, K.N.2
  • 78
    • 0000340764 scopus 로고    scopus 로고
    • A complete basis set model chemistry. VI. Use of density functional geometries and frequencies
    • Montgomery, J. A.; Frisch, M. J., Jr.; Ochterski, J. W.; Petersson, G. A. A Complete Basis Set Model Chemistry. VI. Use of Density Functional Geometries and Frequencies J. Chem. Phys. 1999, 110, 2822-2827 (Pubitemid 129576053)
    • (1999) Journal of Chemical Physics , vol.110 , Issue.2-12 , pp. 2822-2827
    • Montgomery Jr., J.A.1    Frisch, M.J.2    Ochterski, J.W.3    Petersson, G.A.4
  • 79
    • 36749108307 scopus 로고
    • Complete Basis Set Correlation Energies. I the Asymptotic Convergence of Pair Natural Orbital Expansions
    • Nyden, M. R.; Petersson, G. A. Complete Basis Set Correlation Energies. I the Asymptotic Convergence of Pair Natural Orbital Expansions J. Chem. Phys. 1981, 75, 1843-1862
    • (1981) J. Chem. Phys. , vol.75 , pp. 1843-1862
    • Nyden, M.R.1    Petersson, G.A.2
  • 80
    • 0038035472 scopus 로고
    • A Complete Basis Set Model Chemistry. II. Open-shell Systems and the Total Energies of the First-row Atoms
    • Petersson, G. A.; Al-Laham, M. A. A Complete Basis Set Model Chemistry. II. Open-shell Systems and The Total Energies of the First-row Atoms J. Chem. Phys. 1991, 94, 6081-6090
    • (1991) J. Chem. Phys. , vol.94 , pp. 6081-6090
    • Petersson, G.A.1    Al-Laham, M.A.2
  • 81
    • 36449007061 scopus 로고
    • A Complete Basis Set Model Chemistry. III the Complete Basis Set-quadratic Configuration Interaction Family of Methods
    • Petersson, G. A.; Tensfeldt, T. G.; Montgomery, J. A., Jr. A Complete Basis Set Model Chemistry. III the Complete Basis Set-quadratic Configuration Interaction Family of Methods J. Chem. Phys. 1991, 94, 6091-6101
    • (1991) J. Chem. Phys. , vol.94 , pp. 6091-6101
    • Petersson, G.A.1    Tensfeldt, T.G.2    Montgomery, Jr.J.A.3
  • 82
    • 0032558947 scopus 로고    scopus 로고
    • Calibration and comparison of the Gaussian-2, complete basis set, and density functional methods for computational thermochemistry
    • DOI 10.1063/1.477794, PII S002196069831048X
    • Petersson, G. A.; Malick, D. K.; Wilson, W. G.; Ochterski, J. W.; Montgomery, J. A.; Frisch, M. J. Calibration and Comparison of the Gaussian-2, Complete Basis Set, and Density Functional Methods for Computational Thermochemistry J. Chem. Phys. 1998, 109, 10570-10579 (Pubitemid 128675105)
    • (1998) Journal of Chemical Physics , vol.109 , Issue.24 , pp. 10570-10579
    • Petersson, G.A.1    Malick, D.K.2    Wilson, W.G.3    Ochterski, J.W.4    Montgomery Jr., J.A.5    Frisch, M.J.6
  • 83
    • 0006012501 scopus 로고    scopus 로고
    • A Complete Basis Set Model Chemistry. VII. Use of the Minimum Population Localization Method
    • Montgomery, J. A.; Frisch, M. J.; Ochterski, J. W.; Petersson, G. A. A Complete Basis Set Model Chemistry. VII. Use of the Minimum Population Localization Method J. Chem. Phys. 2000, 112, 6532-6541
    • (2000) J. Chem. Phys. , vol.112 , pp. 6532-6541
    • Montgomery, J.A.1    Frisch, M.J.2    Ochterski, J.W.3    Petersson, G.A.4
  • 84
    • 27744489233 scopus 로고    scopus 로고
    • Activation energies of pericyclic reactions: Performance of DFT, MP2, and CBS-QB3 methods for the prediction of activation barriers and reaction energetics of 1,3-dipolar cycloadditions, and revised activation enthalpies for a standard set of hydrocarbon pericyclic reactions
    • DOI 10.1021/jp052504v
    • Ess, D. H.; Houk, K. N. Activation Energies of Pericyclic Reactions: Performance of DFT, MP2, and CBS-QB3Methods for the Prediction of Activation Barriers and Reaction Energetics of 1,3-Dipolar Cycloadditions, and Revised Activation Enthalpies for a Standard Set of Hydrocarbon Pericyclic Reactions J. Phys. Chem. A 2005, 109, 9542-9553 (Pubitemid 41598538)
    • (2005) Journal of Physical Chemistry A , vol.109 , Issue.42 , pp. 9542-9553
    • Ess, D.H.1    Houk, K.N.2
  • 85
    • 0038269037 scopus 로고    scopus 로고
    • A complete basis set model chemistry. V. Extensions to six or more heavy atoms
    • Ochterski, J. W.; Petersson, G. A.; Montgomery, J. A., Jr. A Complete Basis Set Model Chemistry. V. Extensions to Six or More Heavy Atoms J. Chem. Phys. 1996, 104, 2598-2619 (Pubitemid 126747393)
    • (1996) Journal of Chemical Physics , vol.104 , Issue.7 , pp. 2598-2619
    • Ochterski, J.W.1    Petersson, G.A.2    Montgomery Jr., J.A.3
  • 86
    • 40449111562 scopus 로고    scopus 로고
    • Thinking out of the black box: Accurate barrier heights of 1,3-dipolar cycloadditions of ozone with acetylene and ethylene
    • DOI 10.1021/jp710104d
    • Wheeler, S. E.; Ess, D. H.; Houk, K. N. Thinking Out of the Black Box: Accurate Barrier Heights of 1,3-Dipolar Cycloadditions of Ozone with Acetylene and Ethylene J. Phys. Chem. A 2008, 112, 1798-1807 (Pubitemid 351354184)
    • (2008) Journal of Physical Chemistry A , vol.112 , Issue.8 , pp. 1798-1807
    • Wheeler, S.E.1    Ess, D.H.2    Houk, K.N.3
  • 87
    • 0000543185 scopus 로고    scopus 로고
    • Gaussian-3 Theory Using Density Functional Geometries and Zero-point Energies
    • Baboul, A. G.; Curtiss, L. A.; Redfern, P. C.; Raghavachari, K. Gaussian-3 Theory Using Density Functional Geometries and Zero-point Energies J. Chem. Phys. 1999, 110, 7650-7657
    • (1999) J. Chem. Phys. , vol.110 , pp. 7650-7657
    • Baboul, A.G.1    Curtiss, L.A.2    Redfern, P.C.3    Raghavachari, K.4
  • 88
  • 90
    • 0041401966 scopus 로고
    • Gaussian-2 Theory for Molecular Energies of First- and Second-Row Compounds
    • Curtiss, L. A.; Raghavachari, K.; Trucks, G. W.; Pople, J. A. Gaussian-2 Theory for Molecular Energies of First- and Second-Row Compounds J. Chem. Phys. 1991, 94, 7221-7230
    • (1991) J. Chem. Phys. , vol.94 , pp. 7221-7230
    • Curtiss, L.A.1    Raghavachari, K.2    Trucks, G.W.3    Pople, J.A.4
  • 91
    • 0012154673 scopus 로고    scopus 로고
    • Gaussian-3 (G3) theory for molecules containing first and second-row atoms
    • DOI 10.1063/1.477422, PII S0021960698306406
    • Curtiss, L. A.; Raghavachari, K.; Redfern, P. C.; Rassolov, V.; Pople, J. A. Gaussian-3 (G3) Theory for Molecules Containing First and Second-Row Atoms J. Chem. Phys. 1998, 109, 7764-7776 (Pubitemid 128678347)
    • (1998) Journal of Chemical Physics , vol.109 , Issue.18 , pp. 7764-7776
    • Curtiss, L.A.1    Raghavach Ari, K.2    Redfern, P.C.3    Rassolov, V.4    Pople, J.A.5
  • 92
    • 45249099790 scopus 로고    scopus 로고
    • Strength of C-H Bonds at Nitrogen α-Position: Implication for Metabolic Stability of Nitrogen-containing Drug Molecules
    • Meng, X.-M.; Zou, L.-F.; Xie, M.; Fu, Y. Strength of C-H Bonds at Nitrogen α-Position: Implication for Metabolic Stability of Nitrogen-containing Drug Molecules Chin. J. Chem. 2008, 26, 787-793
    • (2008) Chin. J. Chem. , vol.26 , pp. 787-793
    • Meng, X.-M.1    Zou, L.-F.2    Xie, M.3    Fu, Y.4
  • 93
    • 2142819985 scopus 로고    scopus 로고
    • Homolytic C-H and N-H Bond Dissociation Energies of Strained Organic Compounds
    • DOI 10.1021/jo035306d
    • Feng, Y.; Liu, L.; Wang, J.-T.; Zhao, S.-W.; Guo, Q.-X. Homolytic C-H and N-H Bond Dissociation Energies of Strained Organic Compounds J. Org. Chem. 2004, 69, 3129-3138 (Pubitemid 38542566)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.9 , pp. 3129-3138
    • Feng, Y.1    Liu, L.2    Wang, J.-T.3    Zhao, S.-W.4    Guo, Q.-X.5
  • 94
    • 24044444942 scopus 로고    scopus 로고
    • Benchmark calculations of proton affinities and gas-phase basicities of molecules important in the study of biological phosphoryl transfer
    • DOI 10.1039/b504941e
    • Range, K.; Riccardi, D.; Cui, Q.; Elstner, M.; York, D. M. Benchmark Calculations of Proton Affinities and Gas-phase Basicities of Molecules Important in the Study of Biological Phosphoryl Transfer Phys. Chem. Chem. Phys. 2005, 7, 3070-3079 (Pubitemid 41223764)
    • (2005) Physical Chemistry Chemical Physics , vol.7 , Issue.16 , pp. 3070-3079
    • Range, K.1    Riccardi, D.2    Cui, Q.3    Elstner, M.4    York, D.M.5
  • 95
    • 14844360371 scopus 로고    scopus 로고
    • Bond additivity corrections for G3B3 and G3MP2B3 quantum chemistry methods
    • DOI 10.1021/jp0458831
    • Anantharaman, B.; Melius, C. F. Bond Additivity Corrections for G3B3 and G3MP2B3 Quantum Chemistry Methods J. Phys. Chem. A 2005, 109, 1734-1747 (Pubitemid 40352369)
    • (2005) Journal of Physical Chemistry A , vol.109 , Issue.8 , pp. 1734-1747
    • Anantharaman, B.1    Melius, C.F.2


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