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Volumn 8, Issue 1, 2006, Pages 95-98

Sequential pericyclic reaction of ene-diallenes: An efficient approach to the steroid skeleton

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EID: 30944443819     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0525720     Document Type: Article
Times cited : (30)

References (35)
  • 15
    • 85033621680 scopus 로고
    • The tandem formation and intramolecular [4 + 2] cycloaddition of 1-sulfinyl-1-vinylallenes, triggered by [2,3]-sigmatropic rearrangement of the corresponding propargyl sulfenates, has been reported: (a) Okamura, W. H.; Curtin, M. L. Synlett 1990, 1-9.
    • (1990) Synlett , pp. 1-9
    • Okamura, W.H.1    Curtin, M.L.2
  • 22
    • 0030005845 scopus 로고    scopus 로고
    • The intermolecular cycloaddition reaction of the o-quinodimethane, derived from cis-4-octene-2,6-diyne-1,8-diol and benzenesulfenyl chloride, was described in the review article by Grissom (Grissom, J. W.; Gunawardena, G. U.; Klingberg, D.; Huang, D. Tetrahedron 1996, 52, 6453-6518). However, no original manuscript dealing with the details of this reaction is available.
    • (1996) Tetrahedron , vol.52 , pp. 6453-6518
    • Grissom, J.W.1    Gunawardena, G.U.2    Klingberg, D.3    Huang, D.4
  • 33
    • 30944467778 scopus 로고    scopus 로고
    • note
    • In this case, the styrene derivative, a 1,5-hydrogen-shifted product, underwent epoxidation with mCPBA to give 15b.
  • 34
    • 30944457163 scopus 로고    scopus 로고
    • note
    • For determination of the product ratio and the stereochemistries of the cycloadducts, see Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.