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Volumn 11, Issue 10, 2009, Pages 2141-2143

Stereoselective oxindole synthesis by palladium-catalyzed cyclization reaction of 2-(alkynyl)aryl isocyanates with amides

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Indexed keywords


EID: 66149092660     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900759f     Document Type: Article
Times cited : (43)

References (28)
  • 8
    • 66149144036 scopus 로고    scopus 로고
    • N, Kuyper, L. F, Luzzio, M. J, Veal, J. M, Walker, D. H, Glaxo Wellcome Inc, US6387919 Bl, May 14, 2002
    • (b) Davis, S. T.; Dickerson, S. H.; Harris, P. A.; Hunter, R. N.; Kuyper, L. F.; Luzzio, M. J.; Veal, J. M.; Walker, D. H. (Glaxo Wellcome Inc.) US6387919 Bl, May 14, 2002.
    • Davis, S.T.1    Dickerson, S.H.2    Harris, P.A.3    Hunter, R.4
  • 10
    • 66149118711 scopus 로고    scopus 로고
    • Heckel, A.; Roth, G. J.; Kley, J.; Hoerer, S.; Uphues, I. (Boehringer Ingelheim Int.). WO2005087727 Al, September 22, 2006.
    • (d) Heckel, A.; Roth, G. J.; Kley, J.; Hoerer, S.; Uphues, I. (Boehringer Ingelheim Int.). WO2005087727 Al, September 22, 2006.
  • 11
    • 28744455408 scopus 로고    scopus 로고
    • For the synthesis of 3-alkylideneoxindoles by the palladium-catalyzed reaction of 2-(alkynyl)aryl isocyanates, see: Kamijo, S.; Sasaki, Y.; Kanazawa, C.; Schiisseler, T.; Yamamoto, Y. Ansew. Chem. Int. Ed. 2005, 44, 7718.
    • For the synthesis of 3-alkylideneoxindoles by the palladium-catalyzed reaction of 2-(alkynyl)aryl isocyanates, see: Kamijo, S.; Sasaki, Y.; Kanazawa, C.; Schiisseler, T.; Yamamoto, Y. Ansew. Chem. Int. Ed. 2005, 44, 7718.
  • 15
    • 34250838053 scopus 로고    scopus 로고
    • Pinto, A.; Neuville, L.; Zhu, J. Ansew. Chem. Int. Ed. 2007, 46, 3291.
    • (d) Pinto, A.; Neuville, L.; Zhu, J. Ansew. Chem. Int. Ed. 2007, 46, 3291.
  • 20
    • 58149159592 scopus 로고    scopus 로고
    • Miura, T.; Toyoshima, T.; Takahashi, Y.; Murakami, M. Ore. Lett. 2008, 10, 4887. See also:
    • (a) Miura, T.; Toyoshima, T.; Takahashi, Y.; Murakami, M. Ore. Lett. 2008, 10, 4887. See also:
  • 23
    • 66149100654 scopus 로고    scopus 로고
    • The stereochemistry of the exocyclic double bond was assigned by a difference NOE study
    • The stereochemistry of the exocyclic double bond was assigned by a difference NOE study.
  • 24
    • 66149105995 scopus 로고    scopus 로고
    • 7) shifted downfield from 2.45 to 2.76 ppm. However, an attempt to isolate it as solids has been unsuccessful so far.
    • 7) shifted downfield from 2.45 to 2.76 ppm. However, an attempt to isolate it as solids has been unsuccessful so far.
  • 26
    • 66149148406 scopus 로고    scopus 로고
    • 3 gave a complex mixture.
    • 3 gave a complex mixture.
  • 27
    • 66149093180 scopus 로고    scopus 로고
    • Burgdorf, L. T, Bruge, D, Greiner, H, Kordowicz, M, Sirrenberg, C, Zenke, F, Merck Patent GmbH, WO2006131186 Al, December 14, 2006
    • Burgdorf, L. T.; Bruge, D.; Greiner, H.; Kordowicz, M.; Sirrenberg, C.; Zenke, F. (Merck Patent GmbH). WO2006131186 Al, December 14, 2006.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.