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Volumn 40, Issue 5, 1999, Pages 965-968

Concise and efficient total syntheses of (±)-sarcophytols A and B, two antitumor cembrane diterpenoids, by an intramolecular Mcmurry olefination strategy

Author keywords

[No Author keywords available]

Indexed keywords

DITERPENOID; SARCOPHYTOL A; SARCOPHYTOL B;

EID: 0033613741     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02574-X     Document Type: Article
Times cited : (19)

References (41)
  • 5
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    • Japanese patent 81 61317 and 81 61318 to Mitsubishi Kasei Corporation
    • (a) Japanese patent 81 61317 and 81 61318 to Mitsubishi Kasei Corporation; Chem. Abstr. 1981, 95, 169547 and 169548;
  • 6
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    • (a) Japanese patent 81 61317 and 81 61318 to Mitsubishi Kasei Corporation; Chem. Abstr. 1981, 95, 169547 and 169548;
    • (1981) Chem. Abstr. , vol.95 , pp. 169547
  • 9
    • 0013521440 scopus 로고
    • (b) Fijiki, H.; Saganuma, M.; Takagi, K.; et al. In Anticarcinog. Radiat. Prot. 2, [Proc. Int. Conf.], 1989, 3rd, 357; Nygaard, O. F.; Upton, A. C., Ed.; Plenum: New York, 1991; Chem. Abstr. 1992, 117, 184363.
    • (1992) Chem. Abstr. , vol.117 , pp. 184363
  • 12
    • 0013534635 scopus 로고
    • Ph D. Thesis, University of Hawaii
    • For the synthetic studies on sarcophytol A, see: (a)Zou, X.-L; Ph D. Thesis, University of Hawaii, 1995;
    • (1995)
    • Zou, X.-L.1
  • 21
    • 0013521114 scopus 로고
    • Ph D. Thesis, Cornell University
    • (j) Shih, Y.-N.; Ph D. Thesis, Cornell University, 1987.
    • (1987)
    • Shih, Y.-N.1
  • 22
    • 85008140078 scopus 로고
    • For relative stereochemistry and absolute configuration of sarcophytol B, see: Kobayashi, M.; Iesaka, T.; Nakano, E. Chem. Pharm. Bull. 1989, 37, 2053; for the synthetic studies on sarcophytol B, see: (a) McMurry, J. E.; Rico, J. G.; Shih, Y.-N.; Tetrahedron Lett. 1989, 30, 1173;
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 2053
    • Kobayashi, M.1    Iesaka, T.2    Nakano, E.3
  • 23
    • 0024515754 scopus 로고
    • For relative stereochemistry and absolute configuration of sarcophytol B, see: Kobayashi, M.; Iesaka, T.; Nakano, E. Chem. Pharm. Bull. 1989, 37, 2053; for the synthetic studies on sarcophytol B, see: (a) McMurry, J. E.; Rico, J. G.; Shih, Y.-N.; Tetrahedron Lett. 1989, 30, 1173;
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1173
    • McMurry, J.E.1    Rico, J.G.2    Shih, Y.-N.3
  • 25
    • 0013556293 scopus 로고
    • (b) Li, Y.; Li, Y.-L. Gaodeng Xuexiao Huaxue Xuebao (Ch.) 1990, 11, 1218; Chem. Abstr. 1991, 114, 164550.
    • (1991) Chem. Abstr. , vol.114 , pp. 164550
  • 27
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    • For general reviews, see: (a) McMurry, J. E. Chem. Rev. 1989, 89, 1513;
    • (1989) Chem. Rev. , vol.89 , pp. 1513
    • McMurry, J.E.1
  • 32
    • 0013543044 scopus 로고    scopus 로고
    • 13 by silylation(TBSCI, imidazole, DMF, 23 °C, 100%)
    • 13 by silylation(TBSCI, imidazole, DMF, 23 °C, 100%).
  • 34
    • 0013517705 scopus 로고    scopus 로고
    • note
    • +, 1%).
  • 35
    • 0013558005 scopus 로고    scopus 로고
    • Authentic sample was not available for direct comparsion
    • Authentic sample was not available for direct comparsion.
  • 41
    • 0013556920 scopus 로고    scopus 로고
    • Financial support of this work was provided by the National Science Foundation of China (No. 29672015)
    • Financial support of this work was provided by the National Science Foundation of China (No. 29672015).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.