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Volumn 39, Issue 32, 1998, Pages 5875-5876

The intramolecular addition of an aryl radical to a pyridine provides a short entry to toddaquinoline

Author keywords

Cyclisation; Natural products; Polycyclic heterocyclic compounds; Pyridines; Quinolines; Radicals and radical reactions; Wittig reactions

Indexed keywords

ALKALOID; NATURAL PRODUCT; PYRIDINE; RADICAL; TODDAQUINOLINE; UNCLASSIFIED DRUG;

EID: 0032490963     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01187-3     Document Type: Article
Times cited : (42)

References (17)
  • 1
    • 0003622238 scopus 로고
    • National Research Institute of Chinese Medicine, Taiwan
    • 1 Kan, W.S. in Manual of Medicinal Plants in Taiwan, National Research Institute of Chinese Medicine, Taiwan, 1980, p.382.
    • (1980) Manual of Medicinal Plants in Taiwan , pp. 382
    • Kan, W.S.1
  • 4
    • 0010481081 scopus 로고
    • 3 Benzo[h)quinoline and two dimethylbenzo[h]quinolines have been isolated from crude oil: a. Kruber, O.; Raeithel, A. Chem. Ber., 1952, 85, 327;
    • (1952) Chem. Ber. , vol.85 , pp. 327
    • Kruber, O.1    Raeithel, A.2
  • 7
    • 85022940390 scopus 로고
    • Chem. Abstr., 1977, 86, 136297;
    • (1977) Chem. Abstr. , vol.86 , pp. 136297
  • 11
    • 0001216647 scopus 로고
    • 5 The Minisci reaction involves the addition of nucleophilic radicals to protonated pyridines. See a. Curran, D.P. Comp. Org. Synth., 1991, 4, 715. See also
    • (1991) Comp. Org. Synth. , vol.4 , pp. 715
    • Curran, D.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.