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Volumn 64, Issue 5, 2008, Pages 797-808

Gold(I)-catalyzed benzannulation of 3-hydroxy-1,5-enynes: an efficient synthesis of substituted tetrahydronaphthalenes and related compounds

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXY 1,5 ENYNE; DICHLOROMETHANE; GOLD; HYDROXYL GROUP; SILVER DERIVATIVE; TETRALIN DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 37249006898     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.10.084     Document Type: Article
Times cited : (54)

References (76)
  • 1
    • 37249067215 scopus 로고    scopus 로고
    • Selected examples: Dötz benzannulation:
  • 5
    • 37249017089 scopus 로고    scopus 로고
    • Acid-promoted:
  • 8
    • 37249062296 scopus 로고    scopus 로고
    • Anionic cyclization:
  • 12
    • 37249010738 scopus 로고    scopus 로고
    • Metal-catalyzed:
  • 15
    • 37249066341 scopus 로고    scopus 로고
    • Recent reviews on gold-catalyzed reactions:
  • 38
    • 37249045130 scopus 로고    scopus 로고
    • Selected examples:
  • 41
    • 37249082653 scopus 로고    scopus 로고
    • Selected examples:
  • 44
    • 37249001974 scopus 로고    scopus 로고
    • Selected examples:
  • 49
    • 25444517094 scopus 로고    scopus 로고
    • Au salts:
    • Au salts:. Gagosz F. Org. Lett. 7 (2005) 4129
    • (2005) Org. Lett. , vol.7 , pp. 4129
    • Gagosz, F.1
  • 59
    • 37249052935 scopus 로고    scopus 로고
    • 3PAuCl gave low yields.
  • 60
    • 37249031082 scopus 로고    scopus 로고
    • note
    • 3)Cl.
  • 62
    • 37249039629 scopus 로고    scopus 로고
    • Some examples of 6-endo cyclizations of enynes:
  • 66
    • 27144543775 scopus 로고    scopus 로고
    • This product was obtained from 16 via a tandem oxy-Cope/ene reaction. See:
    • This product was obtained from 16 via a tandem oxy-Cope/ene reaction. See:. Warrington J.M., and Barriault L. Org. Lett. 7 (2005) 4589
    • (2005) Org. Lett. , vol.7 , pp. 4589
    • Warrington, J.M.1    Barriault, L.2
  • 67
    • 37249032066 scopus 로고    scopus 로고
    • 1H NMR of the crude mixture.
  • 69
    • 37249033334 scopus 로고    scopus 로고
    • note
    • 1H NMR of the crude mixture. Compound 17 was exposed to TfOH (1 equiv) for 2.5 h at 23 °C, and no degradation products were observed.
  • 70
    • 37249003419 scopus 로고    scopus 로고
    • note
    • 1H NMR. In entry 6, only starting material was recovered.
  • 71
    • 37249023023 scopus 로고    scopus 로고
    • No products from a gold-catalyzed Meyers-Schuster rearrangement were observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.