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Volumn 36, Issue 1, 2003, Pages 66-77

π-nucleophilicity in carbon-carbon bond-forming reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; DIAZONIUM COMPOUND; METAL COMPLEX; ORGANOMETALLIC COMPOUND; POLYCYCLIC AROMATIC HYDROCARBON;

EID: 0037241494     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar020094c     Document Type: Article
Times cited : (888)

References (81)
  • 4
    • 0001290261 scopus 로고
    • Trost, B., M., Fleming, I., Heathcock, C. H., Eds.; Pergamon Press: Oxford
    • Snider, B. B. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Heathcock, C. H., Eds.; Pergamon Press: Oxford, 1991; Vol. 2, pp 527-561.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 527-561
    • Snider, B.B.1
  • 5
    • 33845278941 scopus 로고
    • Characteristics in the reactions of allylsilanes and their applications to versatile synthetic equivalents
    • (a) Hosomi, A. Characteristics in the Reactions of Allylsilanes and Their Applications to Versatile Synthetic Equivalents. Acc. Chem. Res. 1988, 21, 200-206.
    • (1988) Acc. Chem. Res. , vol.21 , pp. 200-206
    • Hosomi, A.1
  • 6
    • 0002324898 scopus 로고
    • The electrophilic substitution of allylsilanes and vinylsilanes
    • Kende, A. S., Ed.; Wiley: New York
    • (b) Fleming, I.; Dunoguès, J.; Smithers, R. The Electrophilic Substitution of Allylsilanes and Vinylsilanes. In Organic Reactions; Kende, A. S., Ed.; Wiley: New York, 1989; Vol. 37, pp 57-575.
    • (1989) Organic Reactions , vol.37 , pp. 57-575
    • Fleming, I.1    Dunoguès, J.2    Smithers, R.3
  • 7
    • 84989487284 scopus 로고
    • Cross-coupling reactions based on acetals
    • (a) Mukaiyama, T.; Murakami, M. Cross-coupling reactions based on acetals. Synthesis 1987, 1043-1054.
    • (1987) Synthesis , pp. 1043-1054
    • Mukaiyama, T.1    Murakami, M.2
  • 8
    • 0001196589 scopus 로고    scopus 로고
    • Diastereoselection in lewis-acid-mediated aldol additions
    • (b) Mahrwald, R. Diastereoselection in Lewis-Acid-Mediated Aldol Additions. Chem. Rev. 1999, 99, 1095-1120.
    • (1999) Chem. Rev. , vol.99 , pp. 1095-1120
    • Mahrwald, R.1
  • 9
    • 0034912138 scopus 로고    scopus 로고
    • Chemistry of propargyldicobalt cations: Recent developments in the Nicholas and related reactions
    • Green, J. R. Chemistry of Propargyldicobalt Cations: Recent Developments in the Nicholas and Related Reactions. Curr. Org. Chem. 2001, 5, 809-826.
    • (2001) Curr. Org. Chem. , vol.5 , pp. 809-826
    • Green, J.R.1
  • 11
    • 0000276556 scopus 로고
    • Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon: Oxford
    • Godleski, S. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 585-661.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 585-661
    • Godleski, S.1
  • 12
    • 33749141140 scopus 로고
    • Scales of nucleophilicity and electrophilicity: A system for ordering polar organic and organometallic reactions
    • (a) Mayr, H.; Patz, M. Scales of Nucleophilicity and Electrophilicity: A System for Ordering Polar Organic and Organometallic Reactions. Angew. Chem., Int. Ed. Engl. 1994, 33, 938-957.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 938-957
    • Mayr, H.1    Patz, M.2
  • 13
    • 0000283970 scopus 로고    scopus 로고
    • Linear free enthalpy relationships: A powerful tool for the design of organic and organometallic synthesis
    • (b) Mayr, H.; Kuhn, O.; Gotta, M. F.; Patz, M. Linear Free Enthalpy Relationships: A Powerful Tool for the Design of Organic and Organometallic Synthesis. J. Phys. Org. Chem. 1998, 11, 642-654.
    • (1998) J. Phys. Org. Chem. , vol.11 , pp. 642-654
    • Mayr, H.1    Kuhn, O.2    Gotta, M.F.3    Patz, M.4
  • 14
    • 0000798274 scopus 로고    scopus 로고
    • Reactivites and selectivities of free and metal-coordinated carbocations
    • (c) Mayr, H.; Patz, M.; Gotta, M. F.; Ofial, A. R. Reactivites and Selectivities of Free and Metal-coordinated Carbocations. Pure Appl. Chem. 1998, 70, 1993-2000.
    • (1998) Pure Appl. Chem. , vol.70 , pp. 1993-2000
    • Mayr, H.1    Patz, M.2    Gotta, M.F.3    Ofial, A.R.4
  • 16
    • 0000347132 scopus 로고
    • Addition reactions of diarylcarbenium ions to 2-methyl-1-pentene: Kinetic method and reaction mechanism
    • Mayr, H.; Schneider, R.; Schade, C.; Bartl, J.; Bederke, R. Addition Reactions of Diarylcarbenium Ions to 2-Methyl-1-pentene: Kinetic Method and Reaction Mechanism. J. Am. Chem. Soc. 1990, 112, 4446-4454.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4446-4454
    • Mayr, H.1    Schneider, R.2    Schade, C.3    Bartl, J.4    Bederke, R.5
  • 17
    • 0000444566 scopus 로고
    • Kinetics of the reactions of allylsilanes, allylgermanes, and allylstannanes with carbenium ions
    • Hagen, G.; Mayr, H. Kinetics of the Reactions of Allylsilanes, Allylgermanes, and Allylstannanes with Carbenium Ions. J. Am. Chem. Soc. 1991, 113, 4954-4961.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4954-4961
    • Hagen, G.1    Mayr, H.2
  • 18
    • 0037130639 scopus 로고    scopus 로고
    • Relationships between carbocation stabilities and electrophilic reactivity parameters E: Quantum mechanical studies of benzhydryl cation structures and stabilities
    • in press (DOI: 10.1021/ja020617b)
    • Schindele, C.; Houk, K. N.; Mayr, H. Relationships Between Carbocation Stabilities and Electrophilic Reactivity Parameters, E: Quantum Mechanical Studies of Benzhydryl Cation Structures and Stabilities. J. Am. Chem. Soc. 2002, 124, in press (DOI: 10.1021/ja020617b).
    • (2002) J. Am. Chem. Soc. , vol.124
    • Schindele, C.1    Houk, K.N.2    Mayr, H.3
  • 19
    • 0000152301 scopus 로고
    • Kinetics of the reactions of the p-methoxy-substituted benzhydryl cation with various alkenes and 1,3-dienes
    • Mayr, H.; Schneider, R.; Irrgang, B.; Schade, C. Kinetics of the Reactions of the p-Methoxy-Substituted Benzhydryl Cation with Various Alkenes and 1,3-Dienes. J. Am. Chem. Soc. 1990, 112, 4454-4459.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4454-4459
    • Mayr, H.1    Schneider, R.2    Irrgang, B.3    Schade, C.4
  • 20
    • 33748225824 scopus 로고
    • Rate constants for the attack of carbenium ions at arenes - A link between the chemistry of aliphatic and aromatic systems
    • Mayr, H.; Bartl, J.; Hagen, G. Rate Constants for the Attack of Carbenium Ions at Arenes - A Link between the Chemistry of Aliphatic and Aromatic Systems. Angew. Chem., Int. Ed. Engl. 1992, 31, 1613-1615.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 1613-1615
    • Mayr, H.1    Bartl, J.2    Hagen, G.3
  • 21
    • 0009548592 scopus 로고
    • Linear free energy and reactivity-selectivity relationships in reactions of diarylcarbenium ions with π-nucleophiles
    • Mayr, H.; Schneider, R.; Grabis, U. Linear Free Energy and Reactivity-Selectivity Relationships in Reactions of Diarylcarbenium Ions with π-Nucleophiles. J. Am. Chem. Soc. 1990, 112, 4460-4467.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4460-4467
    • Mayr, H.1    Schneider, R.2    Grabis, U.3
  • 22
    • 0001066156 scopus 로고    scopus 로고
    • Electrophilic aromatic substitutions of silylated furans and thiophenes with retention of the organosilyl group
    • Herrlich, M.; Hampel, N.; Mayr, H. Electrophilic Aromatic Substitutions of Silylated Furans and Thiophenes with Retention of the Organosilyl Group. Org. Lett. 2001, 3, 1629-1632.
    • (2001) Org. Lett. , vol.3 , pp. 1629-1632
    • Herrlich, M.1    Hampel, N.2    Mayr, H.3
  • 23
    • 0034674742 scopus 로고    scopus 로고
    • Reactions of carbon electrophiles with cobalt-coordinated enynes: Scope and limitations
    • Mayr, H.; Kuhn, O.; Schlierf, C.; Ofial, A. R. Reactions of Carbon Electrophiles with Cobalt-Coordinated Enynes: Scope and Limitations. Tetrahedron 2000, 56, 4219-4229.
    • (2000) Tetrahedron , vol.56 , pp. 4219-4229
    • Mayr, H.1    Kuhn, O.2    Schlierf, C.3    Ofial, A.R.4
  • 24
    • 0026098560 scopus 로고
    • Additions of carbenium ions to nonconjugated dienes. The retarding (-I)-effect of the second double bond
    • Irrgang, B.; Mayr, H. Additions of Carbenium Ions to Nonconjugated Dienes. The Retarding (-I)-Effect of the Second Double Bond. Tetrahedron 1991, 47, 219-228.
    • (1991) Tetrahedron , vol.47 , pp. 219-228
    • Irrgang, B.1    Mayr, H.2
  • 25
    • 0012727126 scopus 로고    scopus 로고
    • Dissertation, TH Darmstadt
    • Roth, M. Dissertation, TH Darmstadt, 1996.
    • (1996)
    • Roth, M.1
  • 26
    • 0142050716 scopus 로고    scopus 로고
    • Comparison of the one-bond nucleophilicities of monomethyl- and dimethyl-substituted 1,3-butadienes
    • Mayr, H.; Hartnagel, M. Comparison of the One-Bond Nucleophilicities of Monomethyl- and Dimethyl-Substituted 1,3-Butadienes. Liebigs Ann. 1996, 2015-2018.
    • (1996) Liebigs Ann. , pp. 2015-2018
    • Mayr, H.1    Hartnagel, M.2
  • 27
    • 0000172777 scopus 로고    scopus 로고
    • Nucleophilic reactivities of tributylstannyl substituted furans and thiophenes
    • Herrlich, M.; Mayr, H.; Faust, R. Nucleophilic Reactivities of Tributylstannyl Substituted Furans and Thiophenes. Org. Lett. 2001, 3, 1633-1635.
    • (2001) Org. Lett. , vol.3 , pp. 1633-1635
    • Herrlich, M.1    Mayr, H.2    Faust, R.3
  • 28
    • 0012664453 scopus 로고    scopus 로고
    • Dissertation, Universität München, 1999
    • Siegmund, T. Dissertation, Universität München, 1999.
    • Siegmund, T.1
  • 29
    • 0032557195 scopus 로고    scopus 로고
    • Determination of the nucleophilicities of silyl and alkyl enol ethers
    • Burfeindt, J.; Patz, M.; Müller, M.; Mayr, H. Determination of the Nucleophilicities of Silyl and Alkyl Enol Ethers. J. Am. Chem. Soc. 1998, 120, 3629-3634.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 3629-3634
    • Burfeindt, J.1    Patz, M.2    Müller, M.3    Mayr, H.4
  • 30
    • 0035804948 scopus 로고    scopus 로고
    • Determination of the nucleophilicities of N,N-bis(silyloxy)enamines
    • Dilman, A. D.; Ioffe, S. L.; Mayr, H. Determination of the Nucleophilicities of N,N-Bis(silyloxy)enamines. J. Org. Chem. 2001, 66, 3196-3200.
    • (2001) J. Org. Chem. , vol.66 , pp. 3196-3200
    • Dilman, A.D.1    Ioffe, S.L.2    Mayr, H.3
  • 31
    • 0012717287 scopus 로고    scopus 로고
    • Dissertation, TH Darmstadt, 1997
    • Hartnagel, M. Dissertation, TH Darmstadt, 1997.
    • Hartnagel, M.1
  • 32
    • 0037008025 scopus 로고    scopus 로고
    • Initiation and propagation rate constants for the cationic polymerization of N-vinylcarbazole
    • Schimmel, H.; Ofial, A. R.; Mayr, H. Initiation and Propagation Rate Constants for the Cationic Polymerization of N-Vinylcarbazole. Macromolecules 2002, 35, 5454-5458.
    • (2002) Macromolecules , vol.35 , pp. 5454-5458
    • Schimmel, H.1    Ofial, A.R.2    Mayr, H.3
  • 33
    • 0012664454 scopus 로고    scopus 로고
    • Unpublished results
    • Kempf, B.; Mayr, H. Unpublished results.
    • Kempf, B.1    Mayr, H.2
  • 34
    • 0028299724 scopus 로고
    • Kinetics of carbenium ion additions to methylenecycloalkanes: Cycloalkyl cation stabilities are not predominantly controlled by strain
    • Roth, M.; Schade, C.; Mayr, H. Kinetics of Carbenium Ion Additions to Methylenecycloalkanes: Cycloalkyl Cation Stabilities Are Not Predominantly Controlled by Strain. J. Org. Chem. 1994, 59, 169-172.
    • (1994) J. Org. Chem. , vol.59 , pp. 169-172
    • Roth, M.1    Schade, C.2    Mayr, H.3
  • 36
    • 0002279813 scopus 로고
    • Electrophilic substitution of heterocycles: Quantitative aspects
    • (b) Heterocyclic compounds: Katritzky, A. R.; Taylor, R. Electrophilic Substitution of Heterocycles: Quantitative Aspects. Adv. Heterocycl. Chem. 1990, 47, 1-467.
    • (1990) Adv. Heterocycl. Chem. , vol.47 , pp. 1-467
    • Katritzky, A.R.1    Taylor, R.2
  • 37
    • 0032567293 scopus 로고    scopus 로고
    • Kinetics of the friedel-crafts alkylations of heterocyclic arenes: Comparison of the nucleophilic reactivities of aromatic and nonaromatic π-systems
    • Gotta, M. F.; Mayr, H. Kinetics of the Friedel-Crafts Alkylations of Heterocyclic Arenes: Comparison of the Nucleophilic Reactivities of Aromatic and Nonaromatic π-Systems. J. Org. Chem. 1998, 63, 9769-9775.
    • (1998) J. Org. Chem. , vol.63 , pp. 9769-9775
    • Gotta, M.F.1    Mayr, H.2
  • 38
    • 0000565741 scopus 로고
    • Kinetics of the reactions of carboxonium ions and aldehyde boron trihalide complexes with alkenes and allylsilanes
    • Mayr, H.; Gorath, G. Kinetics of the Reactions of Carboxonium Ions and Aldehyde Boron Trihalide Complexes with Alkenes and Allylsilanes. J. Am. Chem. Soc. 1995, 117, 7862-7868.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 7862-7868
    • Mayr, H.1    Gorath, G.2
  • 39
    • 0343953389 scopus 로고    scopus 로고
    • 3-substituted α-propargyl cation
    • 3-Substituted α-Propargyl Cation. Tetrahedron 2000, 56, 4149-4155.
    • (2000) Tetrahedron , vol.56 , pp. 4149-4155
    • Netz, A.1    Müller, T.J.J.2
  • 40
    • 0035982111 scopus 로고    scopus 로고
    • Determination of the electrophilic reactivities of 1,1,3-triarylallyl cations
    • Mayr, H.; Fichtner, C.; Ofial, A. R. Determination of the electrophilic reactivities of 1,1,3-triarylallyl cations. J. Chem. Soc., Perkin Trans. 2 2002, 1435-1440.
    • (2002) J. Chem. Soc., Perkin Trans. 2 , pp. 1435-1440
    • Mayr, H.1    Fichtner, C.2    Ofial, A.R.3
  • 42
    • 0000138693 scopus 로고
    • How electrophilic are ferrocenylmethyl cations? Kinetics of their reactions with π-nucleophiles and hydride donors
    • Mayr, H.; Rau, D. How Electrophilic are Ferrocenylmethyl Cations? Kinetics of their Reactions with π-Nucleophiles and Hydride Donors. Chem. Ber. 1994, 127, 2493-2498.
    • (1994) Chem. Ber. , vol.127 , pp. 2493-2498
    • Mayr, H.1    Rau, D.2
  • 43
    • 0035208296 scopus 로고    scopus 로고
    • Kinetics of the reactions of flavylium ions with π-nucleophiles
    • Fichtner, C.; Remennikov, G.; Mayr, H. Kinetics of the Reactions of Flavylium Ions with π-Nucleophiles. Eur. J. Org. Chem. 2001, 4451-4456.
    • (2001) Eur. J. Org. Chem. , pp. 4451-4456
    • Fichtner, C.1    Remennikov, G.2    Mayr, H.3
  • 44
    • 0030923304 scopus 로고    scopus 로고
    • Electrophilicities of iminium ions
    • Mayr, H.; Ofial, A. R. Electrophilicities of Iminium Ions. Tetrahedron Lett. 1997, 38, 3503-3506.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 3503-3506
    • Mayr, H.1    Ofial, A.R.2
  • 45
    • 0032506977 scopus 로고    scopus 로고
    • How electrophilic are cobaltcarbonyl stabilized propargylium ions?
    • Kuhn, O.; Rau, D.; Mayr, H. How Electrophilic Are Cobaltcarbonyl Stabilized Propargylium Ions? J. Am. Chem. Soc. 1998, 120, 900-907.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 900-907
    • Kuhn, O.1    Rau, D.2    Mayr, H.3
  • 46
    • 33748215160 scopus 로고
    • Comparison of the electrophilicity of cationic metal π-complexes and typical carbenium ions
    • Mayr, H.; Müller, K.-H.; Rau, D. Comparison of the Electrophilicity of Cationic Metal π-Complexes and Typical Carbenium ions. Angew. Chem., Int. Ed. Engl. 1993, 32, 1630-1632.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1630-1632
    • Mayr, H.1    Müller, K.-H.2    Rau, D.3
  • 47
    • 0000169185 scopus 로고
    • Electrophilic reactions of some tricarbonylcyclohexadienylium-iron complexes with allyltrimethyl silanes
    • Kelly, L. F.; Narula, A. S.; Birch, A. J. Electrophilic reactions of some tricarbonylcyclohexadienylium-iron complexes with allyltrimethyl silanes. Tetrahedron Lett. 1980, 21, 871-874.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 871-874
    • Kelly, L.F.1    Narula, A.S.2    Birch, A.J.3
  • 49
    • 0006224981 scopus 로고
    • Electrophilic attack at allylsilanes: A quantitative determination of the β-silyl effect
    • (a) Mayr, H.; Pock, R. Electrophilic Attack at Allylsilanes: A Quantitative Determination of the β-Silyl Effect. Tetrahedron 1986, 42, 4211-4214.
    • (1986) Tetrahedron , vol.42 , pp. 4211-4214
    • Mayr, H.1    Pock, R.2
  • 50
    • 0000542616 scopus 로고
    • Relative reaktivität alkyl-substituierter alkene und cycloalkene gegenüber diarylcarbenium-lonen
    • (b) Mayr, H.; Pock, R. Relative Reaktivität Alkyl-substituierter Alkene und Cycloalkene gegenüber Diarylcarbenium-lonen. Chem. Ber. 1986, 119, 2473-2496.
    • (1986) Chem. Ber. , vol.119 , pp. 2473-2496
    • Mayr, H.1    Pock, R.2
  • 51
    • 84984218657 scopus 로고
    • Relative reaktivität konjugierter alkene gegenüber diarylcarbenium-lonen
    • (c) Pock, R.; Mayr, H. Relative Reaktivität konjugierter Alkene gegenüber Diarylcarbenium-lonen. Chem. Ber. 1986, 119, 2497-2509.
    • (1986) Chem. Ber. , vol.119 , pp. 2497-2509
    • Pock, R.1    Mayr, H.2
  • 52
    • 0037123229 scopus 로고    scopus 로고
    • Reactions of carbocations with unsaturated hydrocarbons: Electrophilic alkylation or hydride abstraction?
    • Mayr, H.; Lang, G.; Ofial, A. R. Reactions of Carbocations with Unsaturated Hydrocarbons: Electrophilic Alkylation or Hydride Abstraction? J. Am. Chem. Soc. 2002, 124, 4084-4092.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4084-4092
    • Mayr, H.1    Lang, G.2    Ofial, A.R.3
  • 53
    • 0032517377 scopus 로고    scopus 로고
    • Solvent effects on carbocation-nucleophile combination reactions
    • Richard, J. P.; Szymanski, P.; Williams, K. B. Solvent Effects on Carbocation-Nucleophile Combination Reactions. J. Am. Chem. Soc. 1998, 120, 10372-10378.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 10372-10378
    • Richard, J.P.1    Szymanski, P.2    Williams, K.B.3
  • 54
    • 0001404067 scopus 로고
    • Kinetics of the reactions of laser-flash photolytically generated carbenium ions with alkyl and silyl enol ethers
    • Bartl, J.; Steenken, S.; Mayr, H. Kinetics of the Reactions of Laser-Flash Photolytically Generated Carbenium Ions with Alkyl and Silyl Enol Ethers. J. Am. Chem. Soc. 1991, 113, 7710-7716.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7710-7716
    • Bartl, J.1    Steenken, S.2    Mayr, H.3
  • 55
    • 5244276634 scopus 로고
    • Photo- heterolysis and -homolysis of substituted diphenylmethyl halides, acetates, and phenyl esters in acetonitrile: Characterization of diphenylmethyl cations and radicals generated by 248-nm laser flash photolysis
    • Bartl, J.; Steenken, S.; Mayr, H.; McClelland, R. A. Photo- Heterolysis and -Homolysis of Substituted Diphenylmethyl Halides, Acetates, and Phenyl Esters in Acetonitrile: Characterization of Diphenylmethyl Cations and Radicals Generated by 248-nm Laser Flash Photolysis. J. Am. Chem. Soc. 1990, 112, 6918-6928.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6918-6928
    • Bartl, J.1    Steenken, S.2    Mayr, H.3    McClelland, R.A.4
  • 56
    • 0029968191 scopus 로고    scopus 로고
    • Flash photolysis generation and reactivities of carbenium ions and nitrenium ions
    • McClelland, R. A. Flash Photolysis Generation and Reactivities of Carbenium Ions and Nitrenium Ions. Tetrahedron 1996, 52, 6823-6858.
    • (1996) Tetrahedron , vol.52 , pp. 6823-6858
    • McClelland, R.A.1
  • 57
    • 0001113283 scopus 로고
    • Mechanism of electrophilic aromatic substititions
    • Olah, G. A. Mechanism of Electrophilic Aromatic Substititions. Acc. Chem. Res. 1971, 4, 240-248.
    • (1971) Acc. Chem. Res. , vol.4 , pp. 240-248
    • Olah, G.A.1
  • 61
    • 0345876264 scopus 로고    scopus 로고
    • Faust, R., Shaffer, T. D., Eds.; ACS Symposium Series 665; American Chemical Society: Washington, DC
    • (b) Mayr, H.; Roth, M.; Lang, G. In Cationic Polymerization, Fundamentals and Applications; Faust, R., Shaffer, T. D., Eds.; ACS Symposium Series 665; American Chemical Society: Washington, DC, 1997; pp 25-40.
    • (1997) Cationic Polymerization, Fundamentals and Applications , pp. 25-40
    • Mayr, H.1    Roth, M.2    Lang, G.3
  • 62
    • 0003111769 scopus 로고    scopus 로고
    • Puskas, J. E., Michel, A., Barghi, S., Paulo, C., Eds.; NATO Science Series E, Applied Sciences, Kluwer Academic Publishers: Dordrecht
    • (c) Mayr, H. In Ionic Polymerizations and Related Processes; Puskas, J. E., Michel, A., Barghi, S., Paulo, C., Eds.; NATO Science Series E, Applied Sciences, Vol. 359; Kluwer Academic Publishers: Dordrecht, 1999; pp 99-115.
    • (1999) Ionic Polymerizations and Related Processes , vol.359 , pp. 99-115
    • Mayr, H.1
  • 63
    • 0030576792 scopus 로고    scopus 로고
    • A novel method for the determination of propagation rate constants: Carbocationic oligomerization of isobutylene
    • (a) Roth, M.; Mayr, H. A Novel Method for the Determination of Propagation Rate Constants: Carbocationic Oligomerization of Isobutylene. Macromolecules 1996, 29, 6104-6109.
    • (1996) Macromolecules , vol.29 , pp. 6104-6109
    • Roth, M.1    Mayr, H.2
  • 64
    • 0034290966 scopus 로고    scopus 로고
    • Determination of propagation rate constants in carbocationic polymerization of olefins. 1. Isobutylene
    • (b) Schlaad, H.; Kwon, Y.; Sipos, L.; Faust, R.; Charleux, B. Determination of Propagation Rate Constants in Carbocationic Polymerization of Olefins. 1. Isobutylene. Macromolecules 2000, 33, 8225-8232.
    • (2000) Macromolecules , vol.33 , pp. 8225-8232
    • Schlaad, H.1    Kwon, Y.2    Sipos, L.3    Faust, R.4    Charleux, B.5
  • 65
    • 0003845262 scopus 로고
    • ACS Advances in Chemistry Series 215; American Chemical Society: Washington, DC
    • Nucleophilicity; Harris, J. M., McManus, S. P., Eds.; ACS Advances in Chemistry Series 215; American Chemical Society: Washington, DC, 1987.
    • (1987) Nucleophilicity
    • Harris, J.M.1    McManus, S.P.2
  • 66
    • 0037016457 scopus 로고    scopus 로고
    • Kinetics of carbocation carbanion combinations: Key to a general concept of polar organic reactivity
    • Lucius, R.; Loos, R.; Mayr, H. Kinetics of Carbocation Carbanion Combinations: Key to a General Concept of Polar Organic Reactivity. Angew. Chem., Int. Ed. 2002, 41, 91-95.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 91-95
    • Lucius, R.1    Loos, R.2    Mayr, H.3
  • 67
    • 0035543101 scopus 로고    scopus 로고
    • Formation and stability of carbocations and carbanions in water and intrinsic barriers to their reactions
    • Richard, J. P.; Amyes, T. L.; Toteva, M. M. Formation and Stability of Carbocations and Carbanions in Water and Intrinsic Barriers to Their Reactions. Acc. Chem. Res. 2001, 34, 981-988.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 981-988
    • Richard, J.P.1    Amyes, T.L.2    Toteva, M.M.3
  • 68
    • 33746322935 scopus 로고
    • The coexistence of the reactivity-selectivity principle and of linear free energy relationships
    • Roth, M.; Mayr, H. The Coexistence of the Reactivity-Selectivity Principle and of Linear Free Energy Relationships. Angew. Chem., Int. Ed. Engl. 1995, 34, 2250-2252.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2250-2252
    • Roth, M.1    Mayr, H.2
  • 69
    • 0033591912 scopus 로고    scopus 로고
    • Lifetimes of dialkylcarbocations derived from alkanediazonium ions in solution: Cyclohexadienyl cations as kinetic probes for cation reactivity
    • Pezacki, J. P.; Shukla, D.; Lusztyk, J.; Warkentin, J. Lifetimes of Dialkylcarbocations Derived from Alkanediazonium Ions in Solution: Cyclohexadienyl Cations as Kinetic Probes for Cation Reactivity. J. Am. Chem. Soc. 1999, 121, 6589-6598.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6589-6598
    • Pezacki, J.P.1    Shukla, D.2    Lusztyk, J.3    Warkentin, J.4
  • 70
    • 84985521851 scopus 로고
    • Lewis acid-catalyzed alkylations of carbon-carbon multiple bonds
    • Mayr, H. Lewis Acid-Catalyzed Alkylations of Carbon-Carbon Multiple Bonds. Angew. Chem., Int. Ed. Engl. 1981, 20, 184-186.
    • (1981) Angew. Chem., Int. Ed. Engl. , vol.20 , pp. 184-186
    • Mayr, H.1
  • 71
    • 0012661265 scopus 로고
    • Scope and limitations of aliphatic friedel crafts alkylations. Lewis acid-catalyzed addition reactions of alkyl chlorides to carbon-carbon double bonds
    • Mayr, H.; Striepe, W. Scope and Limitations of Aliphatic Friedel Crafts Alkylations. Lewis Acid-Catalyzed Addition Reactions of Alkyl Chlorides to Carbon-Carbon Double Bonds. J. Org. Chem. 1983, 48, 1159-1165.
    • (1983) J. Org. Chem. , vol.48 , pp. 1159-1165
    • Mayr, H.1    Striepe, W.2
  • 72
    • 33748241860 scopus 로고
    • CC bond formation by addition of carbenium ions to alkenes kinetics and mechanism
    • Mayr, H. CC Bond Formation by Addition of Carbenium Ions to Alkenes: Kinetics and Mechanism. Angew. Chem., Int. Ed. Engl. 1990, 29, 1371-1384.
    • (1990) Angew. Chem., Int. Ed. Engl. , vol.29 , pp. 1371-1384
    • Mayr, H.1
  • 73
    • 0012704745 scopus 로고    scopus 로고
    • Diplomarbeit, Universität München
    • Koszinowski, K. Diplomarbeit, Universität München, 2000.
    • (2000)
    • Koszinowski, K.1
  • 74
    • 0031593029 scopus 로고    scopus 로고
    • NMR spectroscopic evidence for the structure of iminium ion pairs
    • Mayr, H.; Ofial, A. R.; Würthwein, E.-U.; Aust, N. C. NMR Spectroscopic Evidence for the Structure of Iminium Ion Pairs. J. Am. Chem. Soc. 1997, 119, 12727-12733.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12727-12733
    • Mayr, H.1    Ofial, A.R.2    Würthwein, E.-U.3    Aust, N.C.4
  • 76
    • 0012668243 scopus 로고
    • Reactivity of aromatic diazo compounds. VIII. Kinetics of the azo coupling reaction with N,N-dimethylaniline in nonaqueous media
    • Bagal, I. L.; Skvortsov, S. A.; El'tsov, A. V. Reactivity of Aromatic Diazo Compounds. VIII. Kinetics of the Azo Coupling Reaction with N,N-Dimethylaniline in Nonaqueous Media. Zh. Org. Khim. 1978, 14, 361-371.
    • (1978) Zh. Org. Khim. , vol.14 , pp. 361-371
    • Bagal, I.L.1    Skvortsov, S.A.2    El'tsov, A.V.3
  • 78
    • 1542742446 scopus 로고    scopus 로고
    • Quantification of the electrophilicities of diazonium ions
    • Mayr, H.; Hartnagel, M.; Grimm, K. Quantification of the Electrophilicities of Diazonium Ions. Liebigs Ann. 1997, 55-69.
    • (1997) Liebigs Ann. , pp. 55-69
    • Mayr, H.1    Hartnagel, M.2    Grimm, K.3
  • 79
    • 33947090643 scopus 로고
    • Nucleophilic reactivities toward cations
    • Ritchie, C. D. Nucleophilic Reactivities Toward Cations. Acc. Chem. Res. 1972, 5, 348-354.
    • (1972) Acc. Chem. Res. , vol.5 , pp. 348-354
    • Ritchie, C.D.1
  • 80
    • 84879196348 scopus 로고
    • Cation-anion combination reactions. 26. A review
    • Ritchie, C. D. Cation-anion combination reactions. 26. A Review. Can. J. Chem. 1986, 64, 2239-2250.
    • (1986) Can. J. Chem. , vol.64 , pp. 2239-2250
    • Ritchie, C.D.1
  • 81
    • 0000390095 scopus 로고
    • Relative reactivities of carbon-carbon double and triple bonds toward electrophiles
    • Melloni, G.; Modena, G.; Tonellato, U. Relative Reactivities of Carbon-Carbon Double and Triple Bonds toward Electrophiles. Acc. Chem. Res. 1981, 14, 227-233.
    • (1981) Acc. Chem. Res. , vol.14 , pp. 227-233
    • Melloni, G.1    Modena, G.2    Tonellato, U.3


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