메뉴 건너뛰기




Volumn 32, Issue 7, 1999, Pages 571-578

The methylenology principle: How radicals influence the course of ionic reactions

Author keywords

[No Author keywords available]

Indexed keywords

RADICAL;

EID: 0032792653     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar980035s     Document Type: Article
Times cited : (33)

References (60)
  • 2
    • 24644450815 scopus 로고    scopus 로고
    • The tautomerism of indazoline in aqueous solution. A note on the 'principle of vinylogy'
    • (b) Bruneau, P.; Taylor, P. J.; Wilkinson, A. J. The Tautomerism of Indazoline in Aqueous Solution. A Note on the 'Principle of Vinylogy'. J. Chem. Soc., Perkin Trans. 2 1996, 2263.
    • (1996) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 2263
    • Bruneau, P.1    Taylor, P.J.2    Wilkinson, A.J.3
  • 3
    • 84982456595 scopus 로고
    • γ-formyl-tetramethinmerocyanin-, γ-formyl-pentamethincyanin- und [2.2.2]heptamethincyanin-farbstoffe
    • See also the "Methinylogie" principle in (a) Reichardt, C.; Mormann, W. γ-Formyl-Tetramethinmerocyanin-, γ-Formyl-Pentamethincyanin- und [2.2.2]Heptamethincyanin-Farbstoffe. Chem. Ber. 1972, 105, 1815.
    • (1972) Chem. Ber. , vol.105 , pp. 1815
    • Reichardt, C.1    Mormann, W.2
  • 4
    • 84984213181 scopus 로고
    • Über die konformation trinuclearer [2.2.2] heptamethindiiumcyaninfarbstoffe mit indolin-endgruppen
    • (b) Allmann, R.; Grahn, W.; Knecht, J.; Kucharczyk, D.; Reichardt, C. Über die Konformation Trinuclearer [2.2.2] Heptamethindiiumcyaninfarbstoffe mit Indolin-Endgruppen. Chem. Ber. 1985, 118, 1295.
    • (1985) Chem. Ber. , vol.118 , pp. 1295
    • Allmann, R.1    Grahn, W.2    Knecht, J.3    Kucharczyk, D.4    Reichardt, C.5
  • 5
    • 0000468089 scopus 로고
    • Stable simple enols. 3. Static and dynamic NMR behavior of crowded triarylethanols and related compounds. Three-ring-flip as the threshold mechanism for enantiomerization of crowded triarylvinyl propellers
    • See "carbonologues" in Biali, S. E.; Rappoport, Z. Stable Simple Enols. 3. Static and Dynamic NMR Behavior of Crowded Triarylethanols and Related Compounds. Three-Ring-Flip as the Threshold Mechanism for Enantiomerization of Crowded Triarylvinyl Propellers. J. Am. Chem. Soc. 1984, 106, 477.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 477
    • Biali, S.E.1    Rappoport, Z.2
  • 6
    • 0000515511 scopus 로고    scopus 로고
    • Application of the methylenology principle to substitution reactions - A theoretical study
    • Zipse, H. Application of the Methylenology Principle to Substitution Reactions - A Theoretical Study J. Chem. Soc., Perkin Trans. 2 1997, 2691.
    • (1997) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 2691
    • Zipse, H.1
  • 7
    • 33947449188 scopus 로고
    • Aromatic nucleophilic substitution reactions
    • Bunnett, J. F.; Zahler, R. E. Aromatic Nucleophilic Substitution Reactions. Chem. Rev. 1951, 49, 273.
    • (1951) Chem. Rev. , vol.49 , pp. 273
    • Bunnett, J.F.1    Zahler, R.E.2
  • 8
    • 0025168249 scopus 로고
    • 3-Cl(g) and a variational transition-state-theory calculation of the rate constant
    • 3-Cl(g) and a Variational Transition-State-Theory Calculation of the Rate Constant. J. Am. Chem. Soc. 1990, 112, 3338.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 3338
    • Tucker, S.C.1    Truhlar, D.G.2
  • 9
    • 33847090403 scopus 로고
    • Gas-phase nucleophilic displacement reactions
    • Olmstead, W. N.; Brauman, J. I. Gas-Phase Nucleophilic Displacement Reactions. J. Am. Chem. Soc. 1977, 99 4219.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 4219
    • Olmstead, W.N.1    Brauman, J.I.2
  • 10
    • 33845280064 scopus 로고
    • The gas-phase displacement reaction of chloride ion with methyl chloride as a function of kinetic energy
    • Barlow, S. E.; Van Doren, J. M.; Bierbaum, V. M. The Gas-Phase Displacement Reaction of Chloride Ion with Methyl Chloride as a Function of Kinetic Energy. J. Am. Chem. Soc. 1988, 110, 7240.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 7240
    • Barlow, S.E.1    Van Doren, J.M.2    Bierbaum, V.M.3
  • 12
    • 0001255190 scopus 로고
    • N2′ reaction of 3-chloropropene: A theoretical study
    • N2′ Reaction of 3-Chloropropene: A Theoretical Study. J. Am. Chem. Soc. 1985, 107, 1352.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 1352
    • Bach, R.D.1    Wolber, G.J.2
  • 15
    • 33747540974 scopus 로고
    • RN2 pathway - A mechanistic alternative for radicals in protic media?
    • RN2 Pathway - A Mechanistic Alternative for Radicals in Protic Media? Angew. Chem., Int. Ed. Engl. 1994, 33, 1985.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 1985
    • Zipse, H.1
  • 18
    • 0001540102 scopus 로고
    • The quantum mechanical resonance energy of transition states. An indicator of transition state geometry and electronic structure
    • (c) Shaik, S. S.; Duzy, E.; Bartuv, A. The Quantum Mechanical Resonance Energy of Transition States. An Indicator of Transition State Geometry and Electronic Structure. J. Phys. Chem. 1990, 94, 6574.
    • (1990) J. Phys. Chem. , vol.94 , pp. 6574
    • Shaik, S.S.1    Duzy, E.2    Bartuv, A.3
  • 19
    • 0001702058 scopus 로고
    • Transition states, avoided crossing states and valence-bond mixing: Fundamental reactivity paradigms
    • (d) Shaik, S.; Reddy, A. C. Transition States, Avoided Crossing States and Valence-Bond Mixing: Fundamental Reactivity Paradigms. J. Chem. Soc., Faraday Trans. 1994, 90, 1631.
    • (1994) J. Chem. Soc., Faraday Trans. , vol.90 , pp. 1631
    • Shaik, S.1    Reddy, A.C.2
  • 20
    • 0003905492 scopus 로고
    • Bertrán, J., Csizmadia, I. G., Hrsg.; Kluwer Academic Publishers: Dordrecht, The Netherlands
    • Shaik, S. S.; In New Theoretical Concepts for Understanding Organic Reactions; Bertrán, J., Csizmadia, I. G., Hrsg.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1989; pp 165-217.
    • (1989) New Theoretical Concepts for Understanding Organic Reactions , pp. 165-217
    • Shaik, S.S.1
  • 21
    • 0001766175 scopus 로고
    • Ion-molecule reactions of distonic radical cations
    • (a) Stirk, K. M.; Kiminkinen, L. K.; Kenttämaa, H. Ion-Molecule Reactions of Distonic Radical Cations. Chem. Rev. 1992, 92, 1649.
    • (1992) Chem. Rev. , vol.92 , pp. 1649
    • Stirk, K.M.1    Kiminkinen, L.K.2    Kenttämaa, H.3
  • 22
    • 0000397250 scopus 로고    scopus 로고
    • Structure and reactivity of selected distonic radical cations
    • Baer, T., Ng, C. Y., Powis, I., Eds.; Wiley & Sons: New York
    • (b) Smith, R. L; Chou, P. K.; Kenttämaa, H. Structure and Reactivity of Selected Distonic Radical Cations. In The Structure and Dynamics of Organic Ions; Baer, T., Ng, C. Y., Powis, I., Eds.; Wiley & Sons: New York, 1996.
    • (1996) The Structure and Dynamics of Organic Ions
    • Smith, R.L.1    Chou, P.K.2    Kenttämaa, H.3
  • 23
    • 0000557695 scopus 로고
    • The addition of water to ethylene radical cation - A good model system for the reaction of alkene radical cations with nucleophiles?
    • Zipse, H. The Addition of Water to Ethylene Radical Cation - A Good Model System for the Reaction of Alkene Radical Cations with Nucleophiles? J. Am. Chem. Soc. 1995, 117, 11798.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 11798
    • Zipse, H.1
  • 24
    • 37049141009 scopus 로고
    • ESR studies. Part XXXII. Evidence for heterolytic and homolytic transformations of radicals from 1,2-diols and related compounds
    • (a) Gilbert, B. C.; Larkin, J. P.; Norman, R. O. C. ESR Studies. Part XXXII. Evidence for Heterolytic and Homolytic Transformations of Radicals from 1,2-Diols and Related Compounds. J. Chem. Soc., Perkin Trans. 2 1972, 794.
    • (1972) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 794
    • Gilbert, B.C.1    Larkin, J.P.2    Norman, R.O.C.3
  • 25
    • 0017798082 scopus 로고
    • The influence of protonation or alkylation of the phosphate group on the e.s.r. spectra and on the rate of phosphate elimination from 2-methoxyethylphosphate-2-yl radical
    • (b) Behrens, G.; Koltzenburg, G.; Ritter, A.; Schulte-Frohlinde, D. The influence of protonation or alkylation of the phosphate group on the e.s.r. spectra and on the rate of phosphate elimination from 2-methoxyethylphosphate-2-yl radical. Int. J. Radiat. Biol. 1978, 33, 163.
    • (1978) Int. J. Radiat. Biol. , vol.33 , pp. 163
    • Behrens, G.1    Koltzenburg, G.2    Ritter, A.3    Schulte-Frohlinde, D.4
  • 26
    • 0000506428 scopus 로고
    • Fast hydrolysis of alkyl radicals with leaving groups in the β-position
    • (c) Koltzenburg, G.; Behrens, G.; Schulte-Frohlinde, D. Fast Hydrolysis of Alkyl Radicals with Leaving Groups in the β-Position. J. Am. Chem. Soc. 1982, 104, 7311.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7311
    • Koltzenburg, G.1    Behrens, G.2    Schulte-Frohlinde, D.3
  • 27
    • 37049070165 scopus 로고
    • Pulse radiolysis and ESR studies of the dehydration of radicals from 1,2-diols and related compounds
    • (d) Steenken, S.; Davies, M. J.; Gilbert, B. C. Pulse Radiolysis and ESR Studies of the Dehydration of Radicals from 1,2-Diols and Related Compounds. J. Chem. Soc., Perkin Trans. 2 1986, 1003.
    • (1986) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 1003
    • Steenken, S.1    Davies, M.J.2    Gilbert, B.C.3
  • 28
    • 0000697108 scopus 로고    scopus 로고
    • Chemistry of β-(acyloxy)alkyl and β-(phosphatoxy)-alkyl radicals and related species: Radical and radical ionic migrations and fragmentations of carbon-oxygen bonds
    • Beckwith, A. L. J.; Crich, D.; Duggan, P. J.; Yao, Q. Chemistry of β-(Acyloxy)alkyl and β-(Phosphatoxy)-alkyl Radicals and Related Species: Radical and Radical Ionic Migrations and Fragmentations of Carbon-Oxygen Bonds. Chem. Rev. 1997, 97, 3273.
    • (1997) Chem. Rev. , vol.97 , pp. 3273
    • Beckwith, A.L.J.1    Crich, D.2    Duggan, P.J.3    Yao, Q.4
  • 29
    • 0038698181 scopus 로고
    • Model reactions for the degradation of DNA-4′ radicals in aqueous solution. Fast hydrolysis of α-alkoxyalkyl radicals with a leaving group in β-position followed by radical rearrangement and elimination reactions
    • (a) Behrens, G.; Koltzenburg, G.; Schulte-Frohlinde, D. Model Reactions for the Degradation of DNA-4′ Radicals in Aqueous Solution. Fast Hydrolysis of α-Alkoxyalkyl Radicals with a Leaving Group in β-Position Followed by Radical Rearrangement and Elimination Reactions. Z. Naturforsch. C 1982, 37, 1205.
    • (1982) Z. Naturforsch. C , vol.37 , pp. 1205
    • Behrens, G.1    Koltzenburg, G.2    Schulte-Frohlinde, D.3
  • 32
    • 0030929539 scopus 로고    scopus 로고
    • Spectroscopic evidence for a radical cation as intermediate in a model reaction of the 4′-DNA radical strand cleavage
    • Gugger, A.; Batra, R.; Rzadek, P.; Rist, G.; Giese, B. Spectroscopic Evidence for a Radical Cation as Intermediate in a Model Reaction of the 4′-DNA Radical Strand Cleavage. J. Am. Chem. Soc. 1997, 719, 8740.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8740
    • Gugger, A.1    Batra, R.2    Rzadek, P.3    Rist, G.4    Giese, B.5
  • 35
    • 37049040187 scopus 로고
    • Anionotropic systems. Part V. A kinetic investigation of the rearrangement of 1-phenylally esters in non-aqueous solvents
    • (a) Braude, E. A.; Turner, D. W.; Waight, E. S. Anionotropic Systems. Part V. A Kinetic Investigation of the Rearrangement of 1-Phenylally Esters in Non-Aqueous Solvents. J. Chem. Soc. 1958, 2396.
    • (1958) J. Chem. Soc. , pp. 2396
    • Braude, E.A.1    Turner, D.W.2    Waight, E.S.3
  • 36
    • 0000908130 scopus 로고
    • Rearrangement of esters in the gas phase. II. Substituent effects on the rate of isomerization of allylic esters
    • (b) Lewis, E. S.; Hill, J. T.; Newman, E. R. Rearrangement of Esters in the Gas Phase. II. Substituent Effects on the Rate of Isomerization of Allylic Esters. J. Am. Chem. Soc. 1968, 90, 662.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 662
    • Lewis, E.S.1    Hill, J.T.2    Newman, E.R.3
  • 37
    • 37049057003 scopus 로고
    • Intermediates in allylic rearrangements. Part I. The anionotropy of 1- and 3-phenylallyl p-nitrobenzoate
    • Pocker, Y. Intermediates in Allylic Rearrangements. Part I. The Anionotropy of 1- and 3-Phenylallyl p-Nitrobenzoate. J. Chem. Soc. 1958, 4318.
    • (1958) J. Chem. Soc. , pp. 4318
    • Pocker, Y.1
  • 38
    • 0000972941 scopus 로고
    • Free-radical acetoxy group migration
    • (a) Tanner, D. D.; Law, F. C. P. Free-Radical Acetoxy Group Migration. J. Am. Chem. Soc. 1969, 91, 7535.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 7535
    • Tanner, D.D.1    Law, F.C.P.2
  • 39
    • 0000930190 scopus 로고
    • Addition radicalaire d'Esters sur les alcohols èthylèniques
    • (b) Surzur, J. M.; Teissier, P. C. R. Addition radicalaire d'Esters sur les alcohols èthylèniques. C. R. Acad. Sci., Ser. C, Paris 1967, 264, 1981.
    • (1967) C. R. Acad. Sci., Ser. C, Paris , vol.264 , pp. 1981
    • Surzur, J.M.1    Teissier, P.C.R.2
  • 40
    • 0001274370 scopus 로고
    • Mechanism of rearrangement of β-(acyloxy)alkyl radicals
    • (a) Barclay, L. R. C.; Lusztyk, J.; Ingold, K. U. Mechanism of Rearrangement of β-(Acyloxy)alkyl Radicals. J. Am. Chem. Soc. 1984, 106, 1793. (b) Beckwith, A. L J.; Duggan, P. J. The Mechanism of the β-(Acyloxy)alkyl Radical Rearrangement: Substituent and Solvent Effects. J. Am. Chem. Soc. 1996, 118, 12838.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1793
    • Barclay, L.R.C.1    Lusztyk, J.2    Ingold, K.U.3
  • 41
    • 0030464672 scopus 로고    scopus 로고
    • The mechanism of the β-(acyloxy)alkyl radical rearrangement: Substituent and solvent effects
    • (b) Beckwith, A. L J.; Duggan, P. J. The Mechanism of the β-(Acyloxy)alkyl Radical Rearrangement: Substituent and Solvent Effects. J. Am. Chem. Soc. 1996, 118, 12838.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12838
    • Beckwith, A.L.J.1    Duggan, P.J.2
  • 42
    • 37049085326 scopus 로고
    • The mechanism of the β-acyloxyalkyl radical rearrangement. Part 2: β-acyloxytetrahydropyranyl radicals
    • (c) Beckwith, A. L. J.; Duggan, P. J. The Mechanism of the β-Acyloxyalkyl Radical Rearrangement. Part 2: β-Acyloxytetrahydropyranyl Radicals. J. Chem. Soc., Perkin Trans. 2 1993, 1673.
    • (1993) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 1673
    • Beckwith, A.L.J.1    Duggan, P.J.2
  • 44
    • 0001264344 scopus 로고
    • Chemistry of β-(phosphatoxy)alkyl and β-(acyloxy)alkyl radicals. Migration reactions: Scope and stereoselectivity of β-(phosphatoxy)alkyl rearrangement. Mechanism of β-(phosphatoxy)alkyl and β-(acyloxy)alkyl migration
    • (a) Crich, D.; Yao, Q.; Filzen, G. F. Chemistry of β-(Phosphatoxy)alkyl and β-(Acyloxy)alkyl Radicals. Migration Reactions: Scope and Stereoselectivity of β-(Phosphatoxy)alkyl Rearrangement. Mechanism of β-(Phosphatoxy)alkyl and β-(Acyloxy)alkyl Migration. J. Am. Chem. Soc. 1995, 117, 11455.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 11455
    • Crich, D.1    Yao, Q.2    Filzen, G.F.3
  • 45
    • 0000481001 scopus 로고
    • 18O-labelling study of the β-(nitro)alkyl and β-(trifluoracetoxy)alkyl radical migrations: Further examples of a 1,2-shift mechanism
    • 18O-Labelling Study of the β-(Nitro)alkyl and β-(Trifluoracetoxy)alkyl Radical Migrations: Further Examples of a 1,2-Shift Mechanism. J. Org. Chem. 1995, 60, 4834.
    • (1995) J. Org. Chem. , vol.60 , pp. 4834
    • Crich, D.1    Filzen, G.F.2
  • 46
    • 0345031662 scopus 로고
    • The β-(phosphatoxy)alkyl and β-(acyloxy)-alkyl radical rearrangements: Evidence for a non-dissociative mechanism
    • (c) Crich, D.; Yao, Q. The β-(Phosphatoxy)alkyl and β-(Acyloxy)-alkyl Radical Rearrangements: Evidence for a Non-Dissociative Mechanism. J. Am. Chem. Soc. 1994, 116, 2631.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2631
    • Crich, D.1    Yao, Q.2
  • 47
    • 33845469410 scopus 로고
    • Mechanism of 1,2-migration in β-(acyloxy)alkyl radicals
    • (a) Saebo, S.; Beckwith, A. L. J.; Radom, L. Mechanism of 1,2-Migration in β-(Acyloxy)alkyl Radicals. J. Am. Chem. Soc. 1984, 106, 5119.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 5119
    • Saebo, S.1    Beckwith, A.L.J.2    Radom, L.3
  • 48
    • 0000656110 scopus 로고    scopus 로고
    • Acyloxy-shifts in open and closed shell systems -intramolecular nucleophilic substitution reactions in disguise
    • (b) Zipse, H. Acyloxy-Shifts in Open and Closed Shell Systems -Intramolecular Nucleophilic Substitution Reactions in Disguise. J. Chem. Soc., Perkin Trans. 2 1996, 1797.
    • (1996) J. Chem. Soc., Perkin Trans. 2 , vol.2 , pp. 1797
    • Zipse, H.1
  • 49
    • 84962359359 scopus 로고    scopus 로고
    • 1,2-acyloxy shifts in radicals - A computational investigation of substituent and solvent effects
    • (c) Zipse, H. 1,2-Acyloxy Shifts in Radicals - A Computational Investigation of Substituent and Solvent Effects. J. Am. Chem. Soc. 1997, 119, 1087.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 1087
    • Zipse, H.1
  • 50
    • 0000022941 scopus 로고    scopus 로고
    • Beschleunigung der radikalischen 1,2-acyloxyverschiebung (surzur-tanner-umlagerung) durch komplexierung mit lewis-säuren
    • Lacote, E.; Renaud, P. Beschleunigung der radikalischen 1,2-Acyloxyverschiebung (Surzur-Tanner-Umlagerung) durch Komplexierung mit Lewis-Säuren. Angew. Chem. 1998, 110, 2369.
    • (1998) Angew. Chem. , vol.110 , pp. 2369
    • Lacote, E.1    Renaud, P.2
  • 51
    • 0030990622 scopus 로고    scopus 로고
    • Computational insight into the chemistry of β-(phosphatoxy)alkyl radicals: [3,2]- and [1,2]-phosphatoxy rearrangements and a new pathway for syn-elimination of phosphate
    • Zipse, H. Computational Insight into the Chemistry of β-(Phosphatoxy)alkyl Radicals: [3,2]- and [1,2]-Phosphatoxy Rearrangements and a New Pathway for syn-Elimination of Phosphate. J. Am. Chem. Soc. 1997, 119, 2889.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2889
    • Zipse, H.1
  • 52
    • 0345031661 scopus 로고
    • The thermal decomposition of tri-sec-butyl phosphate
    • Higgins, C. E.; Baldwin, W. H. The Thermal Decomposition of Tri-sec-Butyl Phosphate. J. Org. Chem. 1968, 33, 1065.
    • (1968) J. Org. Chem. , vol.33 , pp. 1065
    • Higgins, C.E.1    Baldwin, W.H.2
  • 53
    • 0001080691 scopus 로고
    • Theoretical studies of thermal syn-elimination reactions. The relative rates of ethyl formate, ethyl xanthate, and ethyl phosphinate elimination
    • Erickson, J. A.; Kahn, S. D. Theoretical Studies of Thermal Syn-Elimination Reactions. The Relative Rates of Ethyl Formate, Ethyl Xanthate, and Ethyl Phosphinate Elimination. J. Am. Chem. Soc. 1994, 116, 6271.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 6271
    • Erickson, J.A.1    Kahn, S.D.2
  • 54
    • 33748719327 scopus 로고
    • Mechanism of bleomycin-induced DNA degradation
    • (a) Stubbe, J.; Kozarich, J. Mechanism of Bleomycin-Induced DNA Degradation. Chem. Rev. 1987, 87, 1107.
    • (1987) Chem. Rev. , vol.87 , pp. 1107
    • Stubbe, J.1    Kozarich, J.2
  • 55
    • 12044260107 scopus 로고
    • Mechanism of neocarzinostatin action: Role of DNA microstructure in determination of chemistry of bistranded oxidative damage
    • (b) Goldberg, I. H. Mechanism of Neocarzinostatin Action: Role of DNA Microstructure in Determination of Chemistry of Bistranded Oxidative Damage. Acc. Chem. Res. 1991, 24, 191.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 191
    • Goldberg, I.H.1
  • 59
    • 0038716936 scopus 로고    scopus 로고
    • Chemistry of C-2 glyceryl radicals: Indications for a new mechanism of lipid damage
    • Müller, S. N.; Batra, R.; Senn, M.; Giese, B.; Kisel, M.; Shadyro, O. Chemistry of C-2 Glyceryl Radicals: Indications for a New Mechanism of Lipid Damage. J. Am. Chem. Soc. 1997, 119, 2795.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2795
    • Müller, S.N.1    Batra, R.2    Senn, M.3    Giese, B.4    Kisel, M.5    Shadyro, O.6
  • 60
    • 0022101758 scopus 로고
    • Synthesis with radicals-C-C bond formation via organotin and -mercury compounds
    • Giese, B. Synthesis with Radicals-C-C Bond Formation via Organotin and -mercury Compounds. Angew. Chem., Int. Ed. Engl. 1985, 24, 553.
    • (1985) Angew. Chem., Int. Ed. Engl. , vol.24 , pp. 553
    • Giese, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.