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Volumn 44, Issue 9, 2003, Pages 1859-1862

First formal synthesis of (+)-nimbidiol. Synthesis, X-ray structure and anticancer activity of a novel ring C aromatic diterpene: Dimethyl (+)-podocarpa-8,11,13-triene-12,13-dicarboxylate

Author keywords

Diterpene; Nimbidiol; Podocarpa

Indexed keywords

7 DEOXONIMBIDIOL DIMETHYL ETHER; ANTINEOPLASTIC AGENT; AROMATIC COMPOUND; DIMETHYLPODOCARPA 8,11,13 TRIENE 12,13 DICARBOXYLATE; UNCLASSIFIED DRUG;

EID: 0037463518     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00105-9     Document Type: Article
Times cited : (15)

References (43)
  • 8
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    • Sutherland, J. K. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds. Polyene cyclizations. Pergamon Press: Oxford, 1991; Vol. 3, pp. 341-377.
  • 14
    • 0013077339 scopus 로고    scopus 로고
    • Purchased from Westchem Industries Ltd, Dunedin, New Zealand.
    • Purchased from Westchem Industries Ltd, Dunedin, New Zealand.
  • 18
    • 34147111172 scopus 로고
    • Compound 2: Do Khac Manh, D.; Fetizon, M.; Flament, J. P. Tetrahedron 1975, 31, 1897-1902. Compound 3: Ohloff, G.; Vial, C.; Wolf, H. R.; Jeger, O. Helv. Chim. Acta 1976, 59, 75-81.
    • (1975) Tetrahedron , vol.31 , pp. 1897-1902
    • Do Khac Manh, D.1    Fetizon, M.2    Flament, J.P.3
  • 19
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    • Compound 2: Do Khac Manh, D.; Fetizon, M.; Flament, J. P. Tetrahedron 1975, 31, 1897-1902. Compound 3: Ohloff, G.; Vial, C.; Wolf, H. R.; Jeger, O. Helv. Chim. Acta 1976, 59, 75-81.
    • (1976) Helv. Chim. Acta , vol.59 , pp. 75-81
    • Ohloff, G.1    Vial, C.2    Wolf, H.R.3    Jeger, O.4
  • 23
    • 0013164567 scopus 로고    scopus 로고
    • note
    • 4: C, 73.23; H, 8.19. Found: C, 73.09; H, 7.98.
  • 27
    • 0013123764 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structures in this paper, have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 194600. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk).
  • 31
    • 0000784625 scopus 로고
    • For previous racemic syntheses of 10, see: Harring, S. R.; Livinghouse, T. Tetrahedron Lett. 1989, 30, 1499-1502. Banik, B. K.; Ghosh, S.; Ghatak, U. R. Tetrahedron 1988, 44, 6947-6955.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1499-1502
    • Harring, S.R.1    Livinghouse, T.2
  • 32
    • 0001269674 scopus 로고
    • For previous racemic syntheses of 10, see: Harring, S. R.; Livinghouse, T. Tetrahedron Lett. 1989, 30, 1499-1502. Banik, B. K.; Ghosh, S.; Ghatak, U. R. Tetrahedron 1988, 44, 6947-6955.
    • (1988) Tetrahedron , vol.44 , pp. 6947-6955
    • Banik, B.K.1    Ghosh, S.2    Ghatak, U.R.3
  • 40
    • 0013076032 scopus 로고    scopus 로고
    • 7-Deoxo nimbidiol was rapidly derivatized due to its instability.
    • 7-Deoxo nimbidiol was rapidly derivatized due to its instability.
  • 41
    • 0013075215 scopus 로고    scopus 로고
    • 2=288.2): 288 (35), 245 (100), 273 (32), 191 (33).
    • 2=288.2): 288 (35), 245 (100), 273 (32), 191 (33).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.