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Volumn 47, Issue 35, 2008, Pages 6579-6582

Total syntheses and structural revision of α- and β-diversonolic esters and total syntheses of diversonol and blennolide C

Author keywords

Natural products; Structural reassignment total synthesis; Xanthones

Indexed keywords

CHEMICAL REACTIONS; ESTERIFICATION; ESTERS;

EID: 52449083569     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802632     Document Type: Article
Times cited : (90)

References (17)
  • 8
    • 0037087571 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 996-1000.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 996-1000
  • 9
    • 0027944121 scopus 로고    scopus 로고
    • P. H. Ducrot, J . Y. Lallemand, M. L. Milat, J. P. Blen, Tetrahedron Lett. 1994, 35, 8797-8800. The spectra of 1 and 2 also showed great similarity to those of 18 and 17, respectively.
    • P. H. Ducrot, J . Y. Lallemand, M. L. Milat, J. P. Blen, Tetrahedron Lett. 1994, 35, 8797-8800. The spectra of 1 and 2 also showed great similarity to those of 18 and 17, respectively.
  • 10
    • 53249083471 scopus 로고    scopus 로고
    • CDCC 689919 (2), CDCC 689920 (3), CDCC 689921 (18), and CDCC 689922 (22) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
    • CDCC 689919 (2), CDCC 689920 (3), CDCC 689921 (18), and CDCC 689922 (22) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 12
    • 33748330168 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 307-309.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 307-309
  • 13
    • 53849142171 scopus 로고    scopus 로고
    • W. Zhang, K. Krohn, Z. Ullah, U. Flörke, G. Pescitelli, L. Di Bari, S. Antus, T. Kurtán, J. Rheinheimer, S. Draeger, B. Schulz, Chem. Eur. J. 2008, 14, 4913-4923. These authors recognized that the structure of the diversonoic ester needed to be revised. The spectroscopic data of the synthesized compound 2 were identical to those reported for natural blennolide C.
    • W. Zhang, K. Krohn, Z. Ullah, U. Flörke, G. Pescitelli, L. Di Bari, S. Antus, T. Kurtán, J. Rheinheimer, S. Draeger, B. Schulz, Chem. Eur. J. 2008, 14, 4913-4923. These authors recognized that the structure of the diversonoic ester needed to be revised. The spectroscopic data of the synthesized compound 2 were identical to those reported for natural blennolide C.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.