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Volumn 40, Issue 31, 1999, Pages 5717-5720

Synthesis of indoles: Selenium-catalyzed reductive N-heterocyclization of 2-nitrostyrenes with carbon monoxide

Author keywords

[No Author keywords available]

Indexed keywords

CARBON MONOXIDE; INDOLE DERIVATIVE; SELENIUM; STYRENE DERIVATIVE;

EID: 0033618383     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01080-1     Document Type: Article
Times cited : (40)

References (35)
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    • (a) In The Chemistry of The Alkaloids; S. W. Pelletier, Ed.; Van Nostrand Reinhold Company: New York, 1970, Chapters 9 and 10.
    • (1970) The Chemistry of the Alkaloids
  • 3
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    • A. R. Katritzky, C. W. Rees, Eds.; Pergamon: Oxford
    • (c) In Comprehensive Heterocyclic Chemistry; A. R. Katritzky, C. W. Rees, Eds.; Pergamon: Oxford, 1984, Vol. 4.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.4
  • 4
    • 0000756640 scopus 로고
    • S. D. Barton, W. D. Ollis, Eds.; Pergamon Press: Oxford
    • (d) M. R. Grimmett, In Comprehensive Organic Chemistry; S. D. Barton, W. D. Ollis, Eds.; Pergamon Press: Oxford, 1979, Vol. 4, p 357.
    • (1979) Comprehensive Organic Chemistry , vol.4 , pp. 357
    • Grimmett, M.R.1
  • 5
    • 0000600127 scopus 로고
    • R. H. Wiley, Ed.; Interscience Publisher: New York
    • (e) L. C. Behr, In The Chemistry of Heterocyclic Compounds; R. H. Wiley, Ed.; Interscience Publisher: New York, 1967, Part 3, p 289.
    • (1967) The Chemistry of Heterocyclic Compounds , Issue.PART 3 , pp. 289
    • Behr, L.C.1
  • 9
    • 0004137416 scopus 로고
    • I. Wender, P. Pino, Eds.; Wiley: New York
    • ) For recent reviews see: (a) In Organic Synthesis Via Metal Carbonyls; I. Wender, P. Pino, Eds.; Wiley: New York, 1977, Vol. 2.
    • (1977) Organic Synthesis Via Metal Carbonyls , vol.2
  • 18
    • 0001011833 scopus 로고    scopus 로고
    • and references therein
    • (e) A. M. Tafesh, J. Weiguny, Chem. Rev. 1996, 96, 2035 and references therein.
    • (1996) Chem. Rev. , vol.96 , pp. 2035
    • Tafesh, A.M.1    Weiguny, J.2
  • 28
    • 0009607273 scopus 로고    scopus 로고
    • 4 and evaporation of the solvent gave a yellow residue, which was chromatographed on silica gel to give 2-phenylindole in 76 % yield
    • 4 and evaporation of the solvent gave a yellow residue, which was chromatographed on silica gel to give 2-phenylindole in 76 % yield.
  • 29
    • 0009638830 scopus 로고    scopus 로고
    • In the case of sulfur, the reaction of 1a was not completed under the same reaction conditions as that of selenium to afford 2a in only 19 % yield. On the other hand, tellurium showed no catalytic activity in this reaction at all
    • ) In the case of sulfur, the reaction of 1a was not completed under the same reaction conditions as that of selenium to afford 2a in only 19 % yield. On the other hand, tellurium showed no catalytic activity in this reaction at all.
  • 31
    • 0009601386 scopus 로고    scopus 로고
    • 4d,4e,12
    • 4d,4e,12)
  • 33
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    • 2
    • 2.
  • 34
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    • 15
    • 15)
  • 35
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    • W. Lwowski, John Wiley & Sons: New York, and references therein
    • ) In Nitrenes; W. Lwowski, John Wiley & Sons: New York, 1970 and references therein.
    • (1970) Nitrenes


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.