메뉴 건너뛰기




Volumn 50, Issue 40, 2009, Pages 5628-5630

A versatile synthetic route to 11H-indolo[3,2-c]isoquinolines

Author keywords

Acid catalyzed cyclization; Beckmann rearrangement; Indole; Indoloisoquinoline

Indexed keywords

11H INDOLO[3,2 C]ISOQUINOLINE DERIVATIVE; 2 PHENYLINDOL 3 OXIME DERIVATIVE; INDOLE DERIVATIVE; ISOQUINOLINE DERIVATIVE; OXIME DERIVATIVE; UNCLASSIFIED DRUG;

EID: 68749087217     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.07.107     Document Type: Article
Times cited : (20)

References (30)
  • 3
    • 0010653530 scopus 로고    scopus 로고
    • Thomas E.J. (Ed), Georg Thieme, Stuttgart, Germany
    • Joule J.A. In: Thomas E.J. (Ed). Science of Synthesis Vol. 10 (2000), Georg Thieme, Stuttgart, Germany 361
    • (2000) Science of Synthesis , vol.10 , pp. 361
    • Joule, J.A.1
  • 15
    • 33845452428 scopus 로고    scopus 로고
    • Black D.StC. (Ed), Georg Thieme, Stuttgart, Germany
    • Alvarez M., and Joule J.A. In: Black D.StC. (Ed). Science of Synthesis Vol. 15 (2005), Georg Thieme, Stuttgart, Germany 661
    • (2005) Science of Synthesis , vol.15 , pp. 661
    • Alvarez, M.1    Joule, J.A.2
  • 28
    • 68749107790 scopus 로고    scopus 로고
    • note
    • 2, requires 373.0335.
  • 30
    • 68749090524 scopus 로고    scopus 로고
    • note
    • Crystallographic data for the structure in this Letter have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 718540. X-ray crystal structures were obtained by Mohan Bhadbhade, Crystallography Laboratory, Analytical Centre, The University of New South Wales, Sydney, Australia.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.