메뉴 건너뛰기




Volumn , Issue 4, 2009, Pages 463-465

The asymmetric total synthesis of (-)-securinine

Author keywords

[No Author keywords available]

Indexed keywords


EID: 58149464323     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b816576a     Document Type: Article
Times cited : (37)

References (39)
  • 2
    • 0011311913 scopus 로고
    • R. H. F. Manske, Academic Press, New York, 425-503, and references therein For a recent review of the biological properties of 1, see:
    • V. Snieckus, in The Alkaloids, ed., R. H. F. Manske,, Academic Press, New York, 1973, vol. 14, pp. 425-503, and references therein
    • (1973) The Alkaloids, Ed. , vol.14
    • Snieckus In, V.1
  • 5
    • 0742278884 scopus 로고
    • Ministry of Health of the USSR, 10th edn, Moscow, 612-614
    • Russian Pharmacopeia, Ministry of Health of the USSR, 10th edn, Moscow, 1968, pp. 612-614
    • (1968) Russian Pharmacopeia
  • 6
    • 0023549451 scopus 로고
    • For a general review of various synthetic strategies to the Securinega alkaloids, see:
    • J. A. Beutler A. N. Brubaker Drugs Future 1987 12 957
    • (1987) Drugs Future , vol.12 , pp. 957
    • Beutler, J.A.1    Brubaker, A.N.2
  • 24
    • 2942589152 scopus 로고    scopus 로고
    • For reviews on N-acyl iminium ion chemistry, see:
    • A. Deiters S. F. Martin Chem. Rev. 2004 104 2199 2238
    • (2004) Chem. Rev. , vol.104 , pp. 2199-2238
    • Deiters, A.1    Martin, S.F.2
  • 25
    • 58149465335 scopus 로고    scopus 로고
    • A. Padwa, Georg Thieme Verlag, Stuttgart, 375-439
    • R. A. Pilli and G. B. Rossi, in Science of Synthesis, ed., A. Padwa,, Georg Thieme Verlag, Stuttgart, 2004, vol. 27, pp. 375-439
    • (2004) Science of Synthesis, Ed. , vol.27
    • Pilli, R.A.1    Rossi In, G.B.2
  • 28
    • 0001647908 scopus 로고
    • For a general synthesis of alkynes from aldehydes via the dehydrohalogenation of (Z)-1-iodo-1-alkenes with TBAF, see:
    • G. Stork K. Zhao Tetrahedron Lett. 1989 30 2173 2174
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2173-2174
    • Stork, G.1    Zhao, K.2
  • 38
    • 0742304181 scopus 로고    scopus 로고
    • The previous synthesis of 1 by de March et al. was accomplished in 13 steps and 2.5% overall yield from d-pipecolinic acid; see:
    • T. Honda H. Namiki K. Kaneda H. Mizutani Org. Lett. 2004 6 87 89
    • (2004) Org. Lett. , vol.6 , pp. 87-89
    • Honda, T.1    Namiki, H.2    Kaneda, K.3    Mizutani, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.