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Volumn 2, Issue 18, 2000, Pages 2913-2915

Intramolecular 4 + 3 cycloadditions. Aspects of stereocontrol in the synthesis of cyclooctanoids. A synthesis of (+)-dactylol

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Indexed keywords


EID: 0001444322     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006390b     Document Type: Article
Times cited : (39)

References (36)
  • 1
    • 0030938853 scopus 로고    scopus 로고
    • For recent reviews of 4 + 3 cycloaddition chemistry, see: (a) Harmata, M. Tetrahedron 1997, 53, 6235.
    • (1997) Tetrahedron , vol.53 , pp. 6235
    • Harmata, M.1
  • 2
    • 0001974559 scopus 로고    scopus 로고
    • Lautens, M., Ed.; JAI: Greenwich
    • (b) Harmata, M. In Advances in Cycloaddition; Lautens, M., Ed.; JAI: Greenwich, 1997; Vol. 4, pp 41-86.
    • (1997) Advances in Cycloaddition , vol.4 , pp. 41-86
    • Harmata, M.1
  • 24
    • 0040340191 scopus 로고    scopus 로고
    • note
    • Diene 11 was prepared using Evans' oxazolidinone chemistry. Details will be reported elsewhere.
  • 29
    • 0039155689 scopus 로고    scopus 로고
    • note
    • The ratio was determined by integration of the olefinic region of a crude reaction mixture containing 8 and what appeared to be a single additional cycloadduct (500 MHz). This minor product has not been isolated or characterized.
  • 30
    • 0039748100 scopus 로고    scopus 로고
    • note
    • 2, 0 °C-rt, 48 h, 53%; (d) peracetic acid/NaOAc, 9:1, AcOH, rt, 48 h, 31%; (e) MMPP, 4:1, DMF, rt, 48 h, 84%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.