메뉴 건너뛰기




Volumn 8, Issue 25, 2006, Pages 5905-5908

Gold-catalyzed synthesis of substituted tetrahydronaphthalenes

Author keywords

[No Author keywords available]

Indexed keywords

DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; GOLD; TETRALIN DERIVATIVE;

EID: 33846307425     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol062582g     Document Type: Article
Times cited : (64)

References (32)
  • 1
    • 0032474559 scopus 로고    scopus 로고
    • Selected examples: (a) Cimetiere, B.; Dubuffet, T.; Landras, C.; Descombes, J.-J.; Simonet, S.; Verbeuren, T. J.; Lavielle, G. Bioorg. Med. Chem. Lett. 1998, 8, 1381.
    • Selected examples: (a) Cimetiere, B.; Dubuffet, T.; Landras, C.; Descombes, J.-J.; Simonet, S.; Verbeuren, T. J.; Lavielle, G. Bioorg. Med. Chem. Lett. 1998, 8, 1381.
  • 7
    • 14244263496 scopus 로고    scopus 로고
    • Recent reviews on gold-catalyzed reactions: a
    • Recent reviews on gold-catalyzed reactions: (a) Hoffmann-Röder, A.; Krause, N. Org. Biomol. Chem. 2005, 3, 387.
    • (2005) Org. Biomol. Chem , vol.3 , pp. 387
    • Hoffmann-Röder, A.1    Krause, N.2
  • 11
    • 29544447401 scopus 로고    scopus 로고
    • Cycloisomerization of enynes. For recent reviews, see
    • Cycloisomerization of enynes. For recent reviews, see: Ma, S.; Yu, S.; Gu, Z. Angew. Chem., Int. Ed. 2006, 45, 200.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 200
    • Ma, S.1    Yu, S.2    Gu, Z.3
  • 12
    • 33748792796 scopus 로고    scopus 로고
    • Other recent papers: (a) Lopez, S.; Herrero-Gomez, E.; Perez-Galan, P.; Nieto-Oberhuber, C.; Echavarren, A. M. Angew. Chem., Int. Ed. 2006, 45, 6029.
    • Other recent papers: (a) Lopez, S.; Herrero-Gomez, E.; Perez-Galan, P.; Nieto-Oberhuber, C.; Echavarren, A. M. Angew. Chem., Int. Ed. 2006, 45, 6029.
  • 14
    • 33746299738 scopus 로고    scopus 로고
    • (b) Asao, N. Synlett 2006, 11, 1645.
    • (2006) Synlett , vol.11 , pp. 1645
    • Asao, N.1
  • 19
    • 3242713858 scopus 로고    scopus 로고
    • 2: Harrack, Y.; Blaszykowski, C.; Bernard, M.; Cariou, K.; Mainetti, E.; Mouriès, V.; Dhimane, A.-L.; Fensterbank, L.; Malacria, M. J. Am. Chem. Soc. 2004, 126, 8656.
    • 2: Harrack, Y.; Blaszykowski, C.; Bernard, M.; Cariou, K.; Mainetti, E.; Mouriès, V.; Dhimane, A.-L.; Fensterbank, L.; Malacria, M. J. Am. Chem. Soc. 2004, 126, 8656.
  • 20
    • 33646454721 scopus 로고    scopus 로고
    • 2: Fehr, C.; Farris, I.; Sommer, H. Org. Lett. 2006, 8, 1839.
    • 2: Fehr, C.; Farris, I.; Sommer, H. Org. Lett. 2006, 8, 1839.
  • 22
    • 3242691284 scopus 로고    scopus 로고
    • 2 and Au salts: Mamane, V.; Gress, T.; Krause, H.; Fürstner, A. J. Am. Chem. Soc. 2004, 126, 8654.
    • 2 and Au salts: Mamane, V.; Gress, T.; Krause, H.; Fürstner, A. J. Am. Chem. Soc. 2004, 126, 8654.
  • 23
    • 33746216354 scopus 로고    scopus 로고
    • Pt, Cu, and Au salts: Fehr, C.; Galindo, J. Angew. Chem., Int. Ed. 2006, 45, 2901.
    • (e) Pt, Cu, and Au salts: Fehr, C.; Galindo, J. Angew. Chem., Int. Ed. 2006, 45, 2901.
  • 24
    • 33645688330 scopus 로고    scopus 로고
    • Pt and Au salts: Fürstner, A.; Hannen, P. Chem.-Eur. J. 2006, 12, 3006.
    • (f) Pt and Au salts: Fürstner, A.; Hannen, P. Chem.-Eur. J. 2006, 12, 3006.
  • 30
    • 33846322016 scopus 로고    scopus 로고
    • 1H NMR.
    • 1H NMR.
  • 31
    • 33846279553 scopus 로고    scopus 로고
    • 1H NMR of the crude mixture. Compound 2 was exposed to TfOH (1 equiv) for 2.5 h at 23 °C. and no degradation products were observed.
    • 1H NMR of the crude mixture. Compound 2 was exposed to TfOH (1 equiv) for 2.5 h at 23 °C. and no degradation products were observed.
  • 32
    • 0032486218 scopus 로고    scopus 로고
    • 3)Me is treated with an acid. See: Teles, J. H.; Brode, S.; Chabanas, M. Angew. Chem., Int. Ed. 1998, 37, 1415.
    • 3)Me is treated with an acid. See: Teles, J. H.; Brode, S.; Chabanas, M. Angew. Chem., Int. Ed. 1998, 37, 1415.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.