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Volumn 7, Issue 23, 2005, Pages 5215-5218

Electrophilic behavior of the π delocalized azepinium ion: Friedel-Crafts reactions with benzenes and five-membered aromatic heterocycles

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EID: 28344444686     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol052049l     Document Type: Article
Times cited : (12)

References (40)
  • 17
    • 33947566686 scopus 로고
    • For reviews on Friedel-Crafts reactions, see: (a) Gore, P. Chem. Rev. 1955, 55, 229.
    • (1955) Chem. Rev. , vol.55 , pp. 229
    • Gore, P.1
  • 18
    • 0013343237 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, UK
    • (b) Eyley, S. C. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, UK, 1991; Vol. 2, p 707.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 707
    • Eyley, S.C.1
  • 37
    • 28344436206 scopus 로고    scopus 로고
    • note
    • 4 and phenolic oxygen.
  • 38
    • 28344432228 scopus 로고    scopus 로고
    • note
    • 3 caused the ring-opening reaction of 2-methoxy-2H-azepine 1. Details are described in the Supporting Information.
  • 39
    • 28344452792 scopus 로고    scopus 로고
    • note
    • 3 by the NMR spectrum was unsuccessful due to the paramagnetism of Fe.
  • 40
    • 28344443992 scopus 로고    scopus 로고
    • note
    • 3. Details are described in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.