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Volumn 44, Issue 27, 2003, Pages 5109-5113

Oxidative dearomatization of resorcinol derivatives: Useful conditions leading to valuable cyclohexa-2,5-dienones

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE; CYCLOHEXA 2,5 DIENONE; RESORCINOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0038796986     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01118-3     Document Type: Article
Times cited : (44)

References (35)
  • 15
    • 0038018116 scopus 로고
    • Schultz A.G., Harrington R.E., Holoboski M.A. J. Org. Chem. 57:1992;2973-2976 Whiting, D. A. In Comprehesive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 3, Chapter 3.5, pp. 803-820.
    • (1992) J. Org. Chem. , vol.57 , pp. 2973-2976
    • Schultz, A.G.1    Harrington, R.E.2    Holoboski, M.A.3
  • 22
    • 85031168894 scopus 로고    scopus 로고
    • Additional studies detailing (a) the selection of this particular amide tether, (b) substitiution patterns around the aromatic ring, and (c) enantioselective lactonizations are forthcoming
    • Additional studies detailing (a) the selection of this particular amide tether, (b) substitiution patterns around the aromatic ring, and (c) enantioselective lactonizations are forthcoming.
  • 25
  • 29
    • 85031166311 scopus 로고    scopus 로고
    • 6 was found to be the minor product, formed in a 1:2 ratio with a cyclohexadienone which we were unable to isolate. However, due to the relatively high yield of 6, we believe the cylcohexadienone to be compound which can undergo a [3,3]-sigmatropic rearrangement and tautomerization thereby producing 6 upon chromatography.
    • 6 was found to be the minor product, formed in a 1:2 ratio with a cyclohexadienone which we were unable to isolate. However, due to the relatively high yield of 6, we believe the cylcohexadienone to be compound i which can undergo a [3,3]-sigmatropic rearrangement and tautomerization thereby producing 6 upon chromatography.
  • 33
    • 85031167721 scopus 로고    scopus 로고
    • 1H NMR spectra with only trace amounts of the alcohol 14 present. However, upon chromatography significant amounts of 14 are isolated.
    • 1H NMR spectra with only trace amounts of the alcohol 14 present. However, upon chromatography significant amounts of 14 are isolated.
  • 35
    • 85031169179 scopus 로고    scopus 로고
    • note
    • abstract


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.