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Volumn 8, Issue 11, 2006, Pages 2365-2367

Synthesis of electron deficient 5,6-aryloxy spiroketals

Author keywords

[No Author keywords available]

Indexed keywords

BETA RUBRAMYCIN; BETA-RUBROMYCIN; QUINONE DERIVATIVE; SPIRO COMPOUND;

EID: 33745725806     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0606886     Document Type: Article
Times cited : (57)

References (22)
  • 13
    • 0035905342 scopus 로고    scopus 로고
    • The strategy, which delivered the aglycon of heliquinomycin [Siu, T.; Qin, D. H.; Danishefsky, S. J. Angew. Chem., Int. Ed. 2001, 40, 4713], employs a naphthafuran-3-one nucleus in the spiroketalization. Without the carbonyl, this related system undergoes elimination to the naphthafuran and therefore this strategy is not well suited for the rubromycins that exist in a lower oxidation state.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4713
    • Siu, T.1    Qin, D.H.2    Danishefsky, S.J.3
  • 15
    • 33745730280 scopus 로고    scopus 로고
    • Ph.D. Thesis, University of Pennsylvannia, Philadelphia, PA
    • Waters, S. P. Ph.D. Thesis, University of Pennsylvannia, Philadelphia, PA, 2004.
    • (2004)
    • Waters, S.P.1
  • 22
    • 37049071717 scopus 로고
    • While the rearrangement reported herein seems to resemble the conversion of β-lapachone into α-lapachone, the latter rearrangement requires elevated temperature and harsh contions and results in a loss of optical activity. Bock, K.; Jacobsen, N.; Terem, B. J. Chem. Soc., Perkin Trans, 1 1986, 659-664.
    • (1986) J. Chem. Soc., Perkin Trans, 1 , pp. 659-664
    • Bock, K.1    Jacobsen, N.2    Terem, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.