메뉴 건너뛰기




Volumn 49, Issue 48, 2008, Pages 6749-6751

An expedient synthesis of 3-substituted indoles via reductive alkylation with ketones

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE DERIVATIVE; KETONE DERIVATIVE;

EID: 53649083269     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.034     Document Type: Article
Times cited : (31)

References (12)
  • 4
    • 53649091771 scopus 로고    scopus 로고
    • Attaur, R.; Basha, A. Indole Alkaloids. 1997, p 336.
    • Attaur, R.; Basha, A. Indole Alkaloids. 1997, p 336.
  • 5
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press, New York
    • Sundberg R.J. Indoles (1996), Academic Press, New York
    • (1996) Indoles
    • Sundberg, R.J.1
  • 6
    • 53649097604 scopus 로고    scopus 로고
    • Indoles: The Monoterpenoid Indole Alkaloids, Saxton, J. E., Ed.; The Chemistry of Heterocyclic Compounds; 1983; Vol. 25, Pt. 4, p 886.
    • Indoles: The Monoterpenoid Indole Alkaloids, Saxton, J. E., Ed.; The Chemistry of Heterocyclic Compounds; 1983; Vol. 25, Pt. 4, p 886.
  • 8
    • 53649089123 scopus 로고    scopus 로고
    • Michalak, R. S.; Raveendranath, P. PCT Int. Appl., 2005, WO 2005058820, CA 143:97260.
    • Michalak, R. S.; Raveendranath, P. PCT Int. Appl., 2005, WO 2005058820, CA 143:97260.
  • 11
    • 53649100017 scopus 로고    scopus 로고
    • 3) 7.9 (1H, br s), 7.7 (1H, d), 7.4 (1H), 7.3 (1H, m), 7.2 (1H, m), 7.0 (1H, s), 3.3 (1H, m), 2.2 (2H, m), 1.9 (1H, m), 1.8 (3H, m), 1.0 (1H, m), 1.6 (1H, m)
    • 3) 7.9 (1H, br s), 7.7 (1H, d), 7.4 (1H), 7.3 (1H, m), 7.2 (1H, m), 7.0 (1H, s), 3.3 (1H, m), 2.2 (2H, m), 1.9 (1H, m), 1.8 (3H, m), 1.0 (1H, m), 1.6 (1H, m); HRMS theory 185.1204, found 185.1212.
  • 12
    • 53649102582 scopus 로고    scopus 로고
    • All products were isolated and characterized using NMR, IR, and HRMS.
    • All products were isolated and characterized using NMR, IR, and HRMS.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.