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Volumn 108, Issue 7, 2008, Pages 2265-2299

Modern strategies in electroorganic synthesis

Author keywords

[No Author keywords available]

Indexed keywords

COMBINATORIAL ELECTROCHEMICAL SYNTHESIS; ELECTRO-CHEMICAL REACTION; ELECTRO-ORGANIC SYNTHESIS; ELECTROCHEMICAL DEVICES; ELECTROCHEMICAL PROCESSING; ELECTRON TRANSFER; PRECISE CONTROL; REACTION CONDITIONS; REACTION MEDIUM;

EID: 49049095360     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr0680843     Document Type: Article
Times cited : (1139)

References (459)
  • 3
    • 49049087658 scopus 로고    scopus 로고
    • Kolbe, H. Ann. Chem. Pharm. 1848, 68, 339. (b) Kolbe, H. Ann. Chem. Chem. Pharm.
    • (a) Kolbe, H. Ann. Chem. Pharm. 1848, 68, 339. (b) Kolbe, H. Ann. Chem. Chem. Pharm.
  • 4
    • 33645533693 scopus 로고    scopus 로고
    • 1849, 69, 257. (c) Vijh, A. K.; Conway, B. E. Chem. Rev. 1967, 67, 623.
    • 1849, 69, 257. (c) Vijh, A. K.; Conway, B. E. Chem. Rev. 1967, 67, 623.
  • 9
    • 0008036082 scopus 로고
    • Little, R. D, Weinber, N. L, Eds, Marcel Dekker: New York
    • (e) Little, R. D., Weinber, N. L., Eds. Electroorganic Synthesis; Marcel Dekker: New York, 1991.
    • (1991) Electroorganic Synthesis
  • 10
    • 2042492794 scopus 로고    scopus 로고
    • Hall, N, Ed, University Press: Cambridge
    • (f) Shono, T. In The New Chemistry; Hall, N., Ed.; University Press: Cambridge, 2000.
    • (2000) The New Chemistry
    • Shono, T.1
  • 12
  • 14
    • 0041149565 scopus 로고
    • Selected reviews:(a) Schäfer, H. J
    • Selected reviews:(a) Schäfer, H. J. Angew. Chem., Int. Ed. Engl. 1981, 20, 911.
    • (1981) Angew. Chem., Int. Ed. Engl , vol.20 , pp. 911
  • 20
    • 32344450853 scopus 로고    scopus 로고
    • and references cited therein
    • Itami, K.; Yoshida, J. Synlett 2006, 157, and references cited therein.
    • (2006) Synlett , pp. 157
    • Itami, K.1    Yoshida, J.2
  • 25
    • 0036810317 scopus 로고    scopus 로고
    • and references cited therein
    • (b) Yoshida, J.; Itami, K. Chem. Rev. 2002, 102, 3693, and references cited therein.
    • (2002) Chem. Rev , vol.102 , pp. 3693
    • Yoshida, J.1    Itami, K.2
  • 27
    • 0035888222 scopus 로고    scopus 로고
    • Selected recent examples of electrochemical reductions for organic synthesis: (a) Parrish, J. D.; Little, R. D. Tetrahedron Lett. 2001, 42, 7371.
    • Selected recent examples of electrochemical reductions for organic synthesis: (a) Parrish, J. D.; Little, R. D. Tetrahedron Lett. 2001, 42, 7371.
  • 68
    • 49049105102 scopus 로고    scopus 로고
    • Selected recent examples of electrochemical oxidation of heteroatorn compounds for organic synthesis:a Markó, I. Tetrahedron Lett. 2000, 41, 4383
    • Selected recent examples of electrochemical oxidation of heteroatorn compounds for organic synthesis:a Markó, I. Tetrahedron Lett. 2000, 41, 4383.
  • 95
    • 0012413767 scopus 로고    scopus 로고
    • Selected recent examples:a Whitehead, C. R.; Sessions, E. H.; Ghiviriga, I.; Wright, D. L. Org. Lett. 2002, 4, 3763.
    • Selected recent examples:a Whitehead, C. R.; Sessions, E. H.; Ghiviriga, I.; Wright, D. L. Org. Lett. 2002, 4, 3763.
  • 116
    • 49049108635 scopus 로고    scopus 로고
    • Example of paired electrolysis: a Ishifune, M.; Yamashita, H.; Matsuda, M.; Ishida, H.; Yamashita, N.; Kera, Y.; Kashimura, S.; Masuda, H.; Murase, H. Electrochim. Acta 2001, 46, 3259.
    • Example of paired electrolysis: a Ishifune, M.; Yamashita, H.; Matsuda, M.; Ishida, H.; Yamashita, N.; Kera, Y.; Kashimura, S.; Masuda, H.; Murase, H. Electrochim. Acta 2001, 46, 3259.
  • 121
    • 49049099748 scopus 로고
    • Selected examples:(a) Narasaka, K
    • Selected examples:(a) Narasaka, K. Kohno Bull. Chem. Soc. Jpn. 1993, 66, 3456.
    • (1993) Kohno Bull. Chem. Soc. Jpn , vol.66 , pp. 3456
  • 127
    • 0000586821 scopus 로고    scopus 로고
    • Selected examples:(a) Brumfield, M. A.; Quillen, S. L.; Yoon, U. C.; Mariano, P. S. J. Am. Chem. Soc. 1984, 106, 6855.
    • Selected examples:(a) Brumfield, M. A.; Quillen, S. L.; Yoon, U. C.; Mariano, P. S. J. Am. Chem. Soc. 1984, 106, 6855.
  • 152
    • 0003570337 scopus 로고    scopus 로고
    • Diederich, F, Stang, P. J, Eds, Wiley-VCH: Weinheim
    • Diederich, F., Stang, P. J., Eds. Templated Organic Synthesis; Wiley-VCH: Weinheim, 2000.
    • (2000) Templated Organic Synthesis
  • 161
  • 177
    • 33947232166 scopus 로고    scopus 로고
    • and references cited therein. Review
    • Review: Fuchigami, T. J. Fluorine Chem. 2007, 128, 311, and references cited therein.
    • (2007) Fluorine Chem , vol.128 , pp. 311
    • Fuchigami, T.J.1
  • 254
    • 0024065564 scopus 로고    scopus 로고
    • Electrolysis under high pressure conditions:(a) Bard, A. J.; Flarsheim, W. M.; Johnston, K. P. J. Electrochem. Soc. 1988, 135, 1939.
    • Electrolysis under high pressure conditions:(a) Bard, A. J.; Flarsheim, W. M.; Johnston, K. P. J. Electrochem. Soc. 1988, 135, 1939.
  • 287
    • 46549103031 scopus 로고    scopus 로고
    • Reviews for the synthetic utility of N-acyliminium cations, see:(a) Speckamp, W. N.; Hiemstra, H. Tetrahedron 1985, 41, 4367.
    • Reviews for the synthetic utility of N-acyliminium cations, see:(a) Speckamp, W. N.; Hiemstra, H. Tetrahedron 1985, 41, 4367.
  • 288
    • 0001673091 scopus 로고
    • Trost, B. M, Fleming, I.,Eds, Pergamon Press: Oxford
    • (b) Hiemstra, H.; Speckamp, W. N. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I.,Eds.; Pergamon Press: Oxford, 1991; Vol. 2., p 1047.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 1047
    • Hiemstra, H.1    Speckamp, W.N.2
  • 298
    • 0000590297 scopus 로고    scopus 로고
    • NMR studies of iminium cations have been reported:(a) Yamamoto, Y.; Nakada, T.; Nemoto, H. J. Am. Chem. Soc. 1992, 114, 121.
    • NMR studies of iminium cations have been reported:(a) Yamamoto, Y.; Nakada, T.; Nemoto, H. J. Am. Chem. Soc. 1992, 114, 121.
  • 300
    • 0031593029 scopus 로고    scopus 로고
    • 1H NMR spectroscopy.
    • 1H NMR spectroscopy.
  • 320
    • 49049120052 scopus 로고    scopus 로고
    • The generation of stable ditrityl cations by the oxidative C-C bond cleavage of cyclic compounds has been reported
    • The generation of stable ditrityl cations by the oxidative C-C bond cleavage of cyclic compounds has been reported:
  • 322
    • 0001810217 scopus 로고    scopus 로고
    • Suzuki, T.; Nishida, J.; Tsuji, T. Chem. Commun. 1998, 2193. See also:
    • (b) Suzuki, T.; Nishida, J.; Tsuji, T. Chem. Commun. 1998, 2193. See also:
  • 414
    • 0002684108 scopus 로고
    • Electrosynthesis
    • Baizer, M. M, Lund, H, Eds, 3rd ed, Marcel Dekker: New York
    • (a) Baizer, M. M. Paird Electrosynthesis. In Baizer, M. M., Lund, H., Eds.; Organic Electrochemistry, 3rd ed.; Marcel Dekker: New York, 1991; p 1421.
    • (1991) Organic Electrochemistry , pp. 1421
    • Baizer, M.1    Paird, M.2
  • 442
    • 0001897844 scopus 로고    scopus 로고
    • and references therein, March 3
    • (j) Dagani, R. Chem. Eng. News 1999 (March 3), 51, and references therein.
    • (1999) Chem. Eng. News , pp. 51
    • Dagani, R.1


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