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Volumn 52, Issue 33, 2013, Pages 8736-8741

Total synthesis and structural revision of viridicatumtoxin B

Author keywords

antibiotics; natural products; structural revision; tetracyclines; total synthesis

Indexed keywords

BIOLOGICAL EVALUATION; NATURAL PRODUCTS; STRUCTURAL REVISION; TETRACYCLINES; TOTAL SYNTHESIS;

EID: 84882433588     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201304691     Document Type: Article
Times cited : (27)

References (62)
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    • (2004) Nature , vol.431 , pp. 899-902
    • Nathan, C.1
  • 26
    • 0015590169 scopus 로고
    • We propose that viridicatumtoxin be renamed "viridicatumtoxin A." It has been suggested that viridicatumtoxin A was isolated from Penicillium aethiopicum and not the originally reported Penicillium viridicatum; see
    • R. D. Hutchison, P. S. Steyn, S. J. Van Rensburg, Toxicol. Appl. Pharmacol. 1973, 24, 507-509. We propose that viridicatumtoxin be renamed "viridicatumtoxin A." It has been suggested that viridicatumtoxin A was isolated from Penicillium aethiopicum and not the originally reported Penicillium viridicatum; see
    • (1973) Toxicol. Appl. Pharmacol. , vol.24 , pp. 507-509
    • Hutchison, R.D.1    Steyn, P.S.2    Van Rensburg, S.J.3
  • 46
  • 48
    • 84882382474 scopus 로고    scopus 로고
    • CCDC 941202, 941203, and 945867 contain the supplementary crystallographic data for compounds 23, 29, and 38, respectively for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via. Compounds 23 and 29 were prepared by similar routes to those described herein and will be reported in the full account of this work
    • CCDC 941202, 941203, and 945867 contain the supplementary crystallographic data for compounds 23, 29, and 38, respectively 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. Compounds 23 and 29 were prepared by similar routes to those described herein and will be reported in the full account of this work.
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    • 34249823646 scopus 로고    scopus 로고
    • Electron-rich α-methoxystyrenes are known to be very labile, even at near-neutral pH values; see, for example
    • Electron-rich α-methoxystyrenes are known to be very labile, even at near-neutral pH values; see, for example:, J. P. Richard, K. B. Williams, J. Am. Chem. Soc. 2007, 129, 6952-6961.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 6952-6961
    • Richard, J.P.1    Williams, K.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.