메뉴 건너뛰기




Volumn 2, Issue 2, 2000, Pages 99-102

Total syntheses of (-)-haemanthidine, (+)-pretazettine, and (+)-tazettine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; AMARYLLIDACEAE ALKALOID; ANTINEOPLASTIC AGENT; HEMANTHIDINE; PHENANTHRIDINE DERIVATIVE; PLANT EXTRACT; PRETAZETTINE; TAZETTINE;

EID: 0034719244     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9911472     Document Type: Article
Times cited : (37)

References (41)
  • 2
    • 77956708370 scopus 로고    scopus 로고
    • Cordell, G. A., Ed., Academic Press: New York
    • (b) Hoshino, O. In The Alkaloids; Cordell, G. A., Ed., Academic Press: New York, 1998; Vol. 51, p 323.
    • (1998) The Alkaloids , vol.51 , pp. 323
    • Hoshino, O.1
  • 3
    • 77957033352 scopus 로고
    • Cordell, G. A., Ed., Academic Press: New York
    • (c) Martin, S. F. In The Alkaloids; Cordell, G. A., Ed., Academic Press: New York, 1987; Vol. 30, p 251.
    • (1987) The Alkaloids , vol.30 , pp. 251
    • Martin, S.F.1
  • 24
    • 0000582924 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Elmsford, NY
    • For pertinent reviews of nitrone-alkene cycloaddition reactions, see: (a) Wade, P. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Elmsford, NY, 1991; Vol. 4, pp 1111-1168.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1111-1168
    • Wade, P.A.1
  • 25
    • 0002108906 scopus 로고
    • Padwa, A., Ed.; Wiley-Interscience: New York
    • (b) Tufariello, J. J. In 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley-Interscience: New York, 1984; Vol. 2, pp 83-168.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.2 , pp. 83-168
    • Tufariello, J.J.1
  • 26
    • 0000058602 scopus 로고
    • Padwa, A., Ed.; Wiley-Interscience: New York
    • (c) Padwa, A. In 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley-Interscience: New York, 1984; Vol. 2, pp 277-406.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.2 , pp. 277-406
    • Padwa, A.1
  • 35
    • 0001071115 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Elmsford, NY
    • (b) For a review of Peterson-type olefination reactions, see: Kelly, S. E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Elmsford, NY, 1991; Vol. 1, pp 729-817.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 729-817
    • Kelly, S.E.1
  • 36
    • 0001706485 scopus 로고
    • This equilibration method, originally applied to disubstituted alkenes, has been applied to the trisubstituted analogues for the current work. Details will be provided in due course
    • Schwarz, M.; Graminski, G. F.; Waters, R. M. J. Org. Chem. 1986, 51, 260. This equilibration method, originally applied to disubstituted alkenes, has been applied to the trisubstituted analogues for the current work. Details will be provided in due course.
    • (1986) J. Org. Chem. , vol.51 , pp. 260
    • Schwarz, M.1    Graminski, G.F.2    Waters, R.M.3
  • 37
    • 0022403658 scopus 로고
    • An improved preparation of this material will be reported in the full paper
    • Wovkulich, P. M.; Uskokovic, M. R. Tetrahedron 1985, 41, 3455. An improved preparation of this material will be reported in the full paper.
    • (1985) Tetrahedron , vol.41 , pp. 3455
    • Wovkulich, P.M.1    Uskokovic, M.R.2
  • 38
    • 0013563207 scopus 로고
    • The original assignment of absolute configuration to these alkaloids was based on tenuous circular dichroism studies, eventually confirmed by the conversion of tazettine to (+)-3-methoxyadipic acid (known configuration). Highet, R. J.; Highet, P. F Tetrahedron Lett. 1966, 4099.
    • (1966) Tetrahedron Lett. , pp. 4099
    • Highet, R.J.1    Highet, P.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.