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Volumn 9, Issue 15, 2007, Pages 2955-2958

A general and practical method of alkynyl indole and benzofuran synthesis via tandem Cu- And Pd-catalyzed cross-couplings

Author keywords

[No Author keywords available]

Indexed keywords

BENZOFURAN DERIVATIVE; COPPER; INDOLE DERIVATIVE; PALLADIUM;

EID: 34547187077     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071370w     Document Type: Article
Times cited : (169)

References (29)
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    • For excellent reviews on Pd-catalyzed reactions from industrial laboratories, see: a
    • For excellent reviews on Pd-catalyzed reactions from industrial laboratories, see: (a) Schlummer, B.; Scholz, U. Adv. Synth. Catal. 2004, 346, 1599.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1599
    • Schlummer, B.1    Scholz, U.2
  • 6
    • 34547160305 scopus 로고    scopus 로고
    • For reviews on indole synthesis, see: a, Sundberg, R. J, Ed, Academic Press: San Diego, CA
    • For reviews on indole synthesis, see: (a) Indoles; Sundberg, R. J., Ed.; Academic Press: San Diego, CA, 1996.
    • (1996) Indoles
  • 9
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    • and references therein
    • (d) Humphrey, G. R.; Kuethe, J. T. Chem. Rev. 2006, 106, 2875 and references therein.
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    • Humphrey, G.R.1    Kuethe, J.T.2
  • 10
    • 23944442185 scopus 로고    scopus 로고
    • Indole, azaindole, and thienopyrrole synthesis via Pd-catalyzed tandem C-N/Suzuki-Miyaura couplings: (a) Fang, Y.-Q.; Lautens, M. Org. Lett. 2005, 7, 3549.
    • Indole, azaindole, and thienopyrrole synthesis via Pd-catalyzed tandem C-N/Suzuki-Miyaura couplings: (a) Fang, Y.-Q.; Lautens, M. Org. Lett. 2005, 7, 3549.
  • 12
    • 34447333366 scopus 로고    scopus 로고
    • Fang, Y.-Q.; Yuen, J.; Lautens, M. J. Org. Chem. Published online June 9, 2007 http://dx.doi.org/10.1021/jo07046b. Indole synthesis via tandem C-N/Heck couplings:
    • (c) Fang, Y.-Q.; Yuen, J.; Lautens, M. J. Org. Chem. Published online June 9, 2007 http://dx.doi.org/10.1021/jo07046b. Indole synthesis via tandem C-N/Heck couplings:
  • 13
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    • 4203. Imidazoindolone synthesis via Cucatalyzed double intramolecular amidation
    • (d) Fayol, A.; Fang, Y.-Q.; Lautens, M. Org. Lett. 2006, 8, 4203. Imidazoindolone synthesis via Cucatalyzed double intramolecular amidation:
    • (2006) Org. Lett , vol.8
    • Fayol, A.1    Fang, Y.-Q.2    Lautens, M.3
  • 15
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    • For reviews on benzo[b]furan-containing natural products, see: (a) Donelly, D. M. X.; Meegan, M. J. Furans and Their Benzo Derivatives. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ed.; Pergamon: New York, 1984; 4,. pp 657-712.
    • For reviews on benzo[b]furan-containing natural products, see: (a) Donelly, D. M. X.; Meegan, M. J. Furans and Their Benzo Derivatives. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ed.; Pergamon: New York, 1984; Vol. 4,. pp 657-712.
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    • Bird, C. W.; Cheeseman, G. W. H. Synthesis of Five-membered Rings with One Heteroatom. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ed.; Pergamon: New York, 1984; 4, pp 89-153. For a recent report on benzo[b]furan-containing pharmaceuticals, see:
    • (c) Bird, C. W.; Cheeseman, G. W. H. Synthesis of Five-membered Rings with One Heteroatom. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ed.; Pergamon: New York, 1984; Vol. 4, pp 89-153. For a recent report on benzo[b]furan-containing pharmaceuticals, see:
  • 22
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    • 10% Pd/C (Pearlman) provided by Degussa is marginally better than common 10% Pd/C.
    • 10% Pd/C (Pearlman) provided by Degussa is marginally better than common 10% Pd/C.
  • 23
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    • Pd/C-catalyzed Sonogashira coupling reactions: (a) De la Rosa, M. A.; Velarde, E.; Guzmàn, A. Synth. Commun. 1990, 20, 2059.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.