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Volumn 11, Issue 12, 2013, Pages 1929-1932

Constructions of tetrahydro-γ-carboline skeletons via intramolecular oxidative carbon-carbon bond formation of enamines

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; POSITIVE IONS;

EID: 84876715808     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob00039g     Document Type: Article
Times cited : (15)

References (43)
  • 8
    • 84876699189 scopus 로고
    • WO1994003455, PCT/US1993/006823
    • Rajagopalan and Parthasarathi, WO1994003455, PCT/US1993/006823, 1994
    • (1994)
    • Rajagopalan1    Parthasarathi2
  • 38
    • 84863366903 scopus 로고    scopus 로고
    • For an intramolecular SN2′-type cyclization mechanism for this PhI(OAc)2-mediated oxidative cyclization of N-aryl enamines, see ref. 12
    • M. Zhao F. Wang X. Li Org. Lett. 2012 14 1412
    • (2012) Org. Lett. , vol.14 , pp. 1412
    • Zhao, M.1    Wang, F.2    Li, X.3
  • 42
    • 84943008897 scopus 로고    scopus 로고
    • WO2010057121, PCT/US2009/064637, For our previous work describing the reactions of ArI(OAc)2 with the cyclic N-substituted 3-aminocyclohex-2-enones, analogs of enamine, which afforded the N-arylated α-iodo β-enaminones, see
    • J. R. Allen, M. P. Bourbeau, N. Chen, E. Hu, R. Kunz and S. Rumfelt, WO2010057121, PCT/US2009/064637, 2010
    • (2010) , vol.15
    • Allen, J.R.1    Bourbeau, M.P.2    Chen, N.3    Hu, E.4    Kunz, R.5    Rumfelt, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.