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Volumn 1, Issue 2, 2003, Pages 296-305

Total synthesis of (±)-rhazinal, an alkaloidal spindle toxin from Kopsia teoi

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ALCOHOLS; HYDROGENATION; MOLECULAR STRUCTURE; NEGATIVE IONS; OLEFINS; SINGLE CRYSTALS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); X RAY ANALYSIS;

EID: 0037601344     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b209992f     Document Type: Article
Times cited : (72)

References (50)
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    • A. H. Ratcliffe, PhD Thesis, University of Manchester, 1973.
    • (1973)
    • Ratcliffe, A.H.1
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    • In contrast, intermolecular variants are well known - see for example: R. Lueoend and R. Neier, Helv. Chim. Acta, 1991, 74, 91 and references cited there-in.
    • (1991) Helv. Chim. Acta , vol.74 , pp. 91
    • Lueoend, R.1    Neier, R.2
  • 25
    • 0003288118 scopus 로고    scopus 로고
    • Pyrroles and their benzo derivatives: Reactivity
    • ed. C. W. Bird, Elsevier, Oxford, UK
    • For a recent and comprehensive review of pyrrole chemistry which covers this aspect see: D. St. C. Black, Pyrroles and their benzo derivatives: reactivity, in Comprehensive Heterocyclic Chemistry II, ed. C. W. Bird, Elsevier, Oxford, UK, 1996, vol. 2, pp. 39-117.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 39-117
    • Black, D.St.C.1
  • 26
    • 0034741518 scopus 로고    scopus 로고
    • For related work involving hetero-atom centered nucleophilic capture of π-allylcations generated by electrocyclic ring-opening of gem-dibromocyclopropanes see: M. G. Banwell, J. E. Harvey and K. A. Jolliffe, J. Chem. Soc., Perkin Trans. 1, 2001, 2002 and references cited there-in.
    • (2001) J. Chem. Soc., Perkin Trans. 1 , pp. 2002
    • Banwell, M.G.1    Harvey, J.E.2    Jolliffe, K.A.3
  • 39
    • 0037038994 scopus 로고    scopus 로고
    • The synthesis of compound 31 has been detailed previously (M. G. Banwell and J. A. Smith, J. Chem. Soc., Perkin Trans. 1, 2002, 2613) but is outlined here for the sake of coherence and completeness.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2613
    • Banwell, M.G.1    Smith, J.A.2
  • 44
    • 0037038994 scopus 로고    scopus 로고
    • The synthesis of the acid precursor to compound 38 has been detailed previously (M. G. Banwell and J. A. Smith, J. Chem. Soc., Perkin Trans. 1, 2002, 2613) but is outlined here for the sake of coherence and completeness.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2613
    • Banwell, M.G.1    Smith, J.A.2
  • 46
    • 0041485855 scopus 로고    scopus 로고
    • Aldrich Chemical Company, Cat. No. 12,664-0
    • Aldrich Chemical Company, Cat. No. 12,664-0.
  • 47
    • 0042988492 scopus 로고    scopus 로고
    • Collect data collection software, Nonius B. V.
    • Collect data collection software, Nonius B. V., 1998.
    • (1998)
  • 48
    • 0031059866 scopus 로고    scopus 로고
    • Processing of X-ray diffraction data collected in oscillation mode
    • DENZO-SMN; eds. C. W. Carter, Jr. and R. M. Sweet, Academic Press
    • DENZO-SMN: Z. Otwinowski and W. Minor, Processing of X-ray Diffraction Data Collected in Oscillation Mode, in Methods in Enzymology, Volume 276: Macromolecular Crystallography, Part A, eds. C. W. Carter, Jr. and R. M. Sweet, Academic Press, 1997, pp. 307-326.
    • (1997) Methods in Enzymology, Volume 276: Macromolecular Crystallography, Part A , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.