메뉴 건너뛰기




Volumn 48, Issue 22, 2007, Pages 3775-3778

An approach for quinolines via palladium-catalyzed Heck coupling followed by cyclization

Author keywords

Alkenes; Cyclization; Heck reaction; Palladium catalyst; Quinolines; Quinolones

Indexed keywords

2 IODOANILINE; ALPHA,BETA UNSATURATED CARBONYL DERIVATIVE; ANILINE DERIVATIVE; BASE; CARBONYL DERIVATIVE; PALLADIUM; QUINOLINE DERIVATIVE; QUINOLONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34247648053     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.04.001     Document Type: Article
Times cited : (37)

References (30)
  • 4
    • 1842740801 scopus 로고    scopus 로고
    • For reviews, see:
    • For reviews, see:. Hartwig J.P. Synlett (1997) 329
    • (1997) Synlett , pp. 329
    • Hartwig, J.P.1
  • 15
    • 24144462600 scopus 로고    scopus 로고
    • For our recent report on palladium catalysis:
    • For our recent report on palladium catalysis:. Cho C.S. J. Mol. Cat. A: Chem. 240 (2005) 55
    • (2005) J. Mol. Cat. A: Chem. , vol.240 , pp. 55
    • Cho, C.S.1
  • 17
    • 0033582781 scopus 로고    scopus 로고
    • For our recent report on transition metal-catalyzed synthesis of quinolines:
    • For our recent report on transition metal-catalyzed synthesis of quinolines:. Cho C.S., Oh B.H., and Shim S.C. Tetrahedron Lett. 40 (1999) 1499
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1499
    • Cho, C.S.1    Oh, B.H.2    Shim, S.C.3
  • 25
    • 34247619735 scopus 로고    scopus 로고
    • note
    • Similar treatment of 2-bromoaniline with 2a under the same conditions afforded 3a in only 15% yield.
  • 30
    • 34247603430 scopus 로고    scopus 로고
    • note
    • 3) δ 2.28 (s, 3H), 7.23 (s, 1H), 7.41-7.53 (m, 6H), 7.68 (t, J = 7.5 Hz, 1H), 7.86 (d, J = 8.0 Hz, 1H), 8.09 (d, J = 8.5 Hz, 1H);[...].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.