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Volumn 70, Issue 2, 2005, Pages 713-716

Stereoselective synthesis of the naturally occurring styryllactones (+)-goniofufurone and (+)-cardiobutanolide

Author keywords

[No Author keywords available]

Indexed keywords

BORON; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 12344252564     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0483116     Document Type: Article
Times cited : (48)

References (42)
  • 5
  • 6
    • 0035568886 scopus 로고    scopus 로고
    • Fang, X. P.; Anderson, J. E.; Chang, C. J.; Fanwick, P. E.; McLaughlin, J. L. J. Chem. Soc., Perkin Trans. 1 1990, 1655-1661. For some compounds, these cytotoxic properties have been related to damage of topoisomerase I: López-Lázaro, M.; Martín-Cordero, C.; Bermejo, A.; Cortés, D.; Ayuso, M. J. Anticancer Res. 2001, 21, 3493-3497.
    • (2001) Anticancer Res. , vol.21 , pp. 3493-3497
    • López-Lázaro, M.1    Martín-Cordero, C.2    Bermejo, A.3    Cortés, D.4    Ayuso, M.J.5
  • 7
    • 83155168633 scopus 로고    scopus 로고
    • The 8-acetate (Zhang, Y. J.; Zhou, G. X.; Chen, R. Y.; Yu, D. Q. J. Asian Nat. Prod. Res. 1999, 1, 189-197) and the 7-epimer of goniofufurone (Fang, X. P.; Anderson, J. E.; Chang, C. J.; McLaughlin, J. L.; Fanwick, P. E. J. Nat. Prod. 1991, 54, 1034-1043) are the only other reported natural representatives of the rare furanofurone class within styryllactones. Due to differences in numbering system, the latter compound is named as 7-epi-goniofufurone in some cases (see above), as 8-epi-goniofufurone in others (see ref 2), and even with both forms in others (see ref 5p).
    • (1999) J. Asian Nat. Prod. Res. , vol.1 , pp. 189-197
    • Zhang, Y.J.1    Zhou, G.X.2    Chen, R.Y.3    Yu, D.Q.4
  • 8
    • 0025886241 scopus 로고
    • The 8-acetate (Zhang, Y. J.; Zhou, G. X.; Chen, R. Y.; Yu, D. Q. J. Asian Nat. Prod. Res. 1999, 1, 189-197) and the 7-epimer of goniofufurone (Fang, X. P.; Anderson, J. E.; Chang, C. J.; McLaughlin, J. L.; Fanwick, P. E. J. Nat. Prod. 1991, 54, 1034-1043) are the only other reported natural representatives of the rare furanofurone class within styryllactones. Due to differences in numbering system, the latter compound is named as 7-epi-goniofufurone in some cases (see above), as 8-epi-goniofufurone in others (see ref 2), and even with both forms in others (see ref 5p).
    • (1991) J. Nat. Prod. , vol.54 , pp. 1034-1043
    • Fang, X.P.1    Anderson, J.E.2    Chang, C.J.3    McLaughlin, J.L.4    Fanwick, P.E.5
  • 34
    • 12344316293 scopus 로고    scopus 로고
    • note
    • Acetonide 4 corresponds to compound 9b in ref 7d.
  • 37
    • 0037000811 scopus 로고    scopus 로고
    • (b) For a recent review on asymmetric allylborations, see: Ramachandran, P. V. Aldrichimica Acta 2002, 35, 23-35.
    • (2002) Aldrichimica Acta , vol.35 , pp. 23-35
    • Ramachandran, P.V.1
  • 40
    • 0019119461 scopus 로고
    • Naito, H.; Kawahara, E.; Manila, K.; Maeda, M.; Sasaki, S. J. Org. Chem. 1995, 60, 4419-4427. See also: Fuji, K.; Kawabata, T.; Fujita, E. Chem. Pharm. Bull. 1980, 28, 3662-3664.
    • (1980) Chem. Pharm. Bull. , vol.28 , pp. 3662-3664
    • Fuji, K.1    Kawabata, T.2    Fujita, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.