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Volumn , Issue 6, 2004, Pages 944-950

Gold-catalyzed conjugate addition type reaction of indoles with α,β-enones

Author keywords

Conjugated addition; Gold catalysis; Indoles; , enones

Indexed keywords

BENZYLIDENEACETONE; GOLD; INDOLE DERIVATIVE; KETONE DERIVATIVE;

EID: 3142682149     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-822903     Document Type: Article
Times cited : (129)

References (52)
  • 1
    • 0010653530 scopus 로고    scopus 로고
    • Thomas, E. J., Ed.; Thieme: Stuttgart
    • (a) Joule, J. A. In Science of Synthesis, Vol. 10; Thomas, E. J., Ed.; Thieme: Stuttgart, 2000, 361-652.
    • (2000) Science of Synthesis , vol.10 , pp. 361-652
    • Joule, J.A.1
  • 21
    • 0034605865 scopus 로고    scopus 로고
    • For a recent review on gold catalysis, see: Dyker, G. Angew. Chem. Int. Ed. 2000, 39, 4237.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 4237
    • Dyker, G.1
  • 42
    • 3142752867 scopus 로고    scopus 로고
    • note
    • 2O (5 mol%). The resulting mixture was allotted to react under stirring at r.t. or at 30°C and the reaction was monitored by TLC or GC-MS. After completion, the solvent was removed by evaporation. To the residue, acetone (few mL) was added to precipitate the catalyst, which was separated by filtration. The filtrate was concentrated and the crude products were purified by chromatography on silica gel (230-400 mesh) eluting with n-hexane/EtOAc mixtures.
  • 43
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press: London
    • Sundberg, R. J. In Indoles; Academic Press: London, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 44
    • 3142692753 scopus 로고    scopus 로고
    • note
    • Temperatures are reported as bath temperature.
  • 47
    • 3142670701 scopus 로고    scopus 로고
    • note
    • +], 219 (47).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.