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Volumn 46, Issue 23, 2010, Pages 4076-4078

Synthesis of reaction-ready 6,6′-biindole and 6,6′-biisatin via palladium(ii)-catalysed intramolecular C-H functionalisation

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; INDOLE DERIVATIVE; ISATIN DERIVATIVE; PALLADIUM;

EID: 77953197269     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c002098b     Document Type: Article
Times cited : (14)

References (25)
  • 11
    • 84970546447 scopus 로고
    • 2 in acetic acid resulted in multiple products requiring significant efforts to isolate the components. Our protection/deprotection strategy was high yielding, straightforward, and required no chromatography. Using an isopropyl protecting group gave a 94% yield for bromination after recrystallisation For recent high yielding e.g. in chlorinated solvent see:
    • D. St. C. Black N. Kumar L. C. H. Wong Aust. J. Chem. 1986 39 15 20
    • (1986) Aust. J. Chem. , vol.39 , pp. 15-20
    • St, C.1    Black, C.2    Kumar, N.3    Wong, L.C.H.4
  • 24
    • 0000328509 scopus 로고
    • The synthesis of 6,6′-biindole under a Bischler-type cyclisation was unsuccessful. This acid-catalysed cyclisation was more successful with electron-rich arene such as 3,5-dimethoxyaniline 9
    • V. Gutmann Coord. Chem. Rev. 1976 18 225 255
    • (1976) Coord. Chem. Rev. , vol.18 , pp. 225-255
    • Gutmann, V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.