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Volumn 79, Issue 6, 2014, Pages 2473-2480

Catalytic enantioselective and divergent total synthesis of (+)-10-oxocylindrocarpidine, (+)-cylindrocarpidine, (-)- N - acetylcylindrocarpinol, and (+)-aspidospermine

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ANALYSIS; CATALYSIS; ENANTIOSELECTIVITY;

EID: 84896970595     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402741g     Document Type: Article
Times cited : (35)

References (57)
  • 2
    • 0004230722 scopus 로고    scopus 로고
    • Cordell, G. A. Academic Press: New York, Chapter 9
    • Saxton, J. E. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1998; Vol. 50, Chapter 9.
    • (1998) The Alkaloids , vol.50
    • Saxton, J.E.1
  • 8
    • 0347225187 scopus 로고    scopus 로고
    • Cordell, G. A. Academic Press: San Diego, CA
    • Saxton, J. E. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: San Diego, CA, 1998; Vol. 51, pp 2-1972.
    • (1998) The Alkaloids , vol.51 , pp. 2-1972
    • Saxton, J.E.1
  • 14
    • 37049136857 scopus 로고
    • For a semisynthesis of (+)- N -acetylcylindrocarpinol starting from cylindrocarine and of (-)-10-oxocylindrocarpidine beginning from cylindrocarpidine, see: Gebreyesus, T.; Djerassi, C. J. Chem. Soc., Perkin Trans. 1 1972, 849
    • (1972) J. Chem. Soc., Perkin Trans. 1 , pp. 849
    • Gebreyesus, T.1    Djerassi, C.2
  • 38
    • 84873960658 scopus 로고    scopus 로고
    • This remarkable methodology has been applied to the syntheses of many alkaloids. For a recent example, see: Xie, J.; Wolfe, A. L.; Boger, D. L. Org. Lett. 2013, 15, 868
    • (2013) Org. Lett. , vol.15 , pp. 868
    • Xie, J.1    Wolfe, A.L.2    Boger, D.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.