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Volumn , Issue 22, 2000, Pages 3763-3770

Synthesis of 1-substituted 7-cyano-2,3-diphenylindolizines and evaluation of antioxidant properties

Author keywords

Antioxidants; Biaryls; Cross coupling; Indolizine; Lithiation

Indexed keywords

7 CYANO 2,3 DIPHENYLINDOLIZIN 1 YL ACETATE; 7 CYANO 2,3 DIPHENYLINDOLIZIN 1 YL TRIFLATE; 7 CYANO 2,3 DIPHENYLINDOLIZINE; ANTIOXIDANT; ASCORBIC ACID; FERRIC SULFATE; INDOLIZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033678403     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200011)2000:22<3763::AID-EJOC3763>3.0.CO;2-S     Document Type: Article
Times cited : (130)

References (24)
  • 1
    • 0025940277 scopus 로고
    • [1a] B. Halliwell, Drugs 1991, 42, 569-605. -
    • (1991) Drugs , vol.42 , pp. 569-605
    • Halliwell, B.1
  • 15
    • 0000418343 scopus 로고    scopus 로고
    • For other recent examples of cleavage of aryl triflates to phenols under Pd-catalysed coupling conditions, see for instance: [8a] J. P. Wolfe, S. L. Buchwald, J. Org. Chem. 1997, 62, 1264-1267. -
    • (1997) J. Org. Chem. , vol.62 , pp. 1264-1267
    • Wolfe, J.P.1    Buchwald, S.L.2
  • 24
    • 0007052248 scopus 로고    scopus 로고
    • note
    • Lown and Matsumoto actually reported the synthesis of 3-chloro-5-azaindolizine from 5-azaindolizin-3-ol (ref. [5]), but Weidner et al. later showed that the hydroxy group must have been situated in the indolizine 1-position, see ref. [2d].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.