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Volumn 73, Issue 14, 2008, Pages 5536-5541

Synthesis of the common propellane core structure of the hasubanan alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CHEMICAL REACTIONS; DERIVATIVES; ESTERS; ORGANIC COMPOUNDS;

EID: 48249093797     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800793s     Document Type: Article
Times cited : (27)

References (46)
  • 16
    • 48249129911 scopus 로고    scopus 로고
    • Patent number WO2004000815, International publication date Dec 31, 2003
    • (e) Qin, G.-W.; Tang, X.-C.; Caignard, D.-H.; Renard, P.; Lestage, P. Patent number WO2004000815, International publication date Dec 31, 2003.
    • Qin, G.-W.1    Tang, X.-C.2    Caignard, D.-H.3    Renard, P.4    Lestage, P.5
  • 29
    • 9344260283 scopus 로고    scopus 로고
    • (a) Bernd, P. J. Org. Chem. 2004, 69, 8287-8296.
    • (2004) J. Org. Chem , vol.69 , pp. 8287-8296
    • Bernd, P.1
  • 32
    • 0042285952 scopus 로고    scopus 로고
    • (d) Bernd, P. J. Org. Chem. 2003, 68, 7123-7125.
    • (2003) J. Org. Chem , vol.68 , pp. 7123-7125
    • Bernd, P.1
  • 34
    • 48249146436 scopus 로고    scopus 로고
    • The reaction was accompanied by 10% yield of the O-alkylated product below. (Chemical Equation Presented)
    • The reaction was accompanied by 10% yield of the O-alkylated product below. (Chemical Equation Presented)
  • 39
    • 48249134226 scopus 로고    scopus 로고
    • Upon hydrocyanation of imine 13, the unstable aminonitrile intermediate was acetylated by using AcCl (10.0 equiv) and TEA (1.0 equiv) in DCM as a 0.04 M solution to provide 56% yield of the desired 14a over 4 steps from 11.
    • Upon hydrocyanation of imine 13, the unstable aminonitrile intermediate was acetylated by using AcCl (10.0 equiv) and TEA (1.0 equiv) in DCM as a 0.04 M solution to provide 56% yield of the desired 14a over 4 steps from 11.
  • 40
    • 48249086406 scopus 로고    scopus 로고
    • 3 in MeOH.
    • 3 in MeOH.
  • 42
    • 22244475751 scopus 로고    scopus 로고
    • For recent reviews on the application of N-acylbenzotriazole in organic synthesis, see:(a) Katritzky, A. R.; Suzuki, K.; Wang, Z. Synlett 2005, 11, 1656-1665.
    • For recent reviews on the application of N-acylbenzotriazole in organic synthesis, see:(a) Katritzky, A. R.; Suzuki, K.; Wang, Z. Synlett 2005, 11, 1656-1665.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.