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Volumn 1, Issue 1, 1999, Pages 79-81

An enantioselective total synthesis of (+)-geissoschizine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; CARBOLINE DERIVATIVE; GEISSOSCHIZINE; MANNICH BASE;

EID: 0033564999     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990554a     Document Type: Article
Times cited : (102)

References (56)
  • 3
    • 0041610625 scopus 로고
    • Saxton, J. E., Ed.; Wiley-Interscience: New York, Part Four (The Monoterpenoid Indole Alkaloids), Chapter 3
    • For general reviews of the structure and synthesis of indole alkaloids of the Corynantheine-Heteroyohimbine group, see: (a) Brown, R. T. In Indoles; Saxton, J. E., Ed.; Wiley-Interscience: New York, 1983; Part Four (The Monoterpenoid Indole Alkaloids), Chapter 3.
    • (1983) Indoles
    • Brown, R.T.1
  • 5
    • 0003540638 scopus 로고
    • Saxton, J. E., Ed.; Wiley-Interscience: New York, Supplement to Chapter 3
    • (c) Lounasmaa, M.; Tolvanen, A. In Monoterpenoid Indole Alkaloids; Saxton, J. E., Ed.; Wiley-Interscience: New York, 1994; Supplement to Vol. 25, Part 4, Chapter 3.
    • (1994) Monoterpenoid Indole Alkaloids , vol.25 , Issue.4 PART
    • Lounasmaa, M.1    Tolvanen, A.2
  • 7
    • 0043113425 scopus 로고
    • Saxton, J. E., Ed.; Wiley-Interscience: New York, Part Four (The Monoterpenoid Indole Alkaloids). Chapter 1
    • (b) Herbert, R. B. In Indoles; Saxton, J. E., Ed.; Wiley-Interscience: New York, 1983; Part Four (The Monoterpenoid Indole Alkaloids). Chapter 1.
    • (1983) Indoles
    • Herbert, R.B.1
  • 9
    • 11844275743 scopus 로고
    • Saxton, J. E., Ed.; Wiley-Interscience: New York, Supplement to Chapter 1
    • (d) Herbert, R. B. In Monoterpenoid Indole Alkaloids; Saxton, J. E., Ed.; Wiley-Interscience: New York, 1994; Supplement to Vol. 25, Part 4, Chapter 1.
    • (1994) Monoterpenoid Indole Alkaloids , vol.25 , Issue.4 PART
    • Herbert, R.B.1
  • 31
    • 0027130840 scopus 로고
    • For other recent applications of vinylogous Mannich reactions to alkaloid synthesis, see: (a) Martin, S. F.; Liras, S. J. Am. Chem. Soc. 1993, 115, 10450.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10450
    • Martin, S.F.1    Liras, S.2
  • 40
    • 0042612529 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR, MS) characteristics. Analytical samples of all new compounds were obtained by distillation, recrystallization, or preparative HPLC or TLC and gave satisfactory combustion analysis (C, H) and/or identification by high-resolution mass spectrometry. All yields are based on isolated, purified materials.
  • 56
    • 85088669817 scopus 로고    scopus 로고
    • note
    • 6b


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