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Volumn 52, Issue 31, 1996, Pages 10347-10362

Synthesis of a cancer growth-inhibiting diterpene-stereoselective formal synthesis of (+)-aphidicolin

Author keywords

[No Author keywords available]

Indexed keywords

APHIDICOLIN;

EID: 0030605909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00575-3     Document Type: Article
Times cited : (21)

References (51)
  • 6
    • 0003027336 scopus 로고
    • Elsevier
    • 6. The terms topology and topography are defined as follows. Thus, the relationship between hirsutene and capnellene is a topographical one (i.e. identical ring system, but different disposition of substituents). While, the relationship between pentalenene and hirsutene is a topological one (i.e. different ring system, but similar disposition of identical substituents). Hudlicky, T.; Rulin, F.; Lovelace, T. C.; Reed, J. W. Studies in Natural Products Chemistry, Elsevier, 1989, 3, pp 3-72.
    • (1989) Studies in Natural Products Chemistry , vol.3 , pp. 3-72
    • Hudlicky, T.1    Rulin, F.2    Lovelace, T.C.3    Reed, J.W.4
  • 10
    • 85030202193 scopus 로고    scopus 로고
    • Personal information from Dr. Anthony B. Mauger (National Cancer Institute)
    • 10. Personal information from Dr. Anthony B. Mauger (National Cancer Institute).
  • 11
    • 85030206630 scopus 로고    scopus 로고
    • (Nippon Mektron Ltd.). Japan Patent Kokai Tokkyo Koho JP 5-310621
    • 11. Hiramitsu, T.; Mouri, A.; Suzuki, H. (Nippon Mektron Ltd.). Japan Patent Kokai Tokkyo Koho JP 5-310621.
    • Hiramitsu, T.1    Mouri, A.2    Suzuki, H.3
  • 20
    • 0023879655 scopus 로고
    • (f) Bettolo, R. M.; Tagliatesta, P.; Lupi, A.; Bravetti, D. Helv. Chim. Acta 1983, 66, 1922-1928; Lupi, A.; Patamia, M.; Bettolo, R. M. ibid. 1988, 71, 872-875.
    • (1988) Helv. Chim. Acta , vol.71 , pp. 872-875
    • Lupi, A.1    Patamia, M.2    Bettolo, R.M.3
  • 24
    • 0023687356 scopus 로고
    • Formal Syntheses of Aphidicolin: (i) Tanis, S. P.; Chuang, Y.-H.; Head, D. B. Tetrahedron Lett. 1985, 26, 6147-6150; idem J. Org. Chem. 1988, 53, 4929-4938.
    • (1988) J. Org. Chem. , vol.53 , pp. 4929-4938
    • Tanis, S.P.1    Chuang, Y.-H.2    Head, D.B.3
  • 29
    • 85047671779 scopus 로고
    • (m) Toyota, M.; Nishikawa, Y.; Fukumoto, K. Tetrahedron Lett. 1995, 36, 5379-5382. Recent Synthetic Approaches to Stemodane Diterpenes: (n) White, J. D.; Somers, T. C. J. Am. Chem. Soc. 1994, 116, 9912-9920, and references cited therein.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5379-5382
    • Toyota, M.1    Nishikawa, Y.2    Fukumoto, K.3
  • 30
    • 0028007329 scopus 로고
    • and references cited therein
    • (m) Toyota, M.; Nishikawa, Y.; Fukumoto, K. Tetrahedron Lett. 1995, 36, 5379-5382. Recent Synthetic Approaches to Stemodane Diterpenes: (n) White, J. D.; Somers, T. C. J. Am. Chem. Soc. 1994, 116, 9912-9920, and references cited therein.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 9912-9920
    • White, J.D.1    Somers, T.C.2
  • 36
  • 45
    • 0001314041 scopus 로고
    • 22. Taber, D. F.; Saleh, S. A. J. Am. Chem. Soc. 1980, 102, 5085-5088; Taber, D. F.; Campbell, C.; Gunn, B. P.; Chiu, I-C. Tetrahdron Lett. 1981, 22, 5141-5144.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5085-5088
    • Taber, D.F.1    Saleh, S.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.