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Volumn 8, Issue 9, 2006, Pages 1889-1891

Epoxysilane rearrangement induced by a carbanion generated by conjugate addition of enolates of chloroacetate and α-chloroacetamides: Formation of functionalized cyclopropane derivatives

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EID: 33646446917     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol060469k     Document Type: Article
Times cited : (21)

References (26)
  • 10
    • 0035835953 scopus 로고    scopus 로고
    • For the use of Brook rearrangement in tandem bond formation strategies, see: (d) Moser, W. H. Tetrahedron 2001, 57, 2065-2084.
    • (2001) Tetrahedron , vol.57 , pp. 2065-2084
    • Moser, W.H.1
  • 13
    • 0003152616 scopus 로고
    • Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Moody, C. J., Eds.; Pergamon: Oxford
    • (g) Qi, H.; Curran, D. P. In Comprehensive Organic Functional Group Transformations; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Moody, C. J., Eds.; Pergamon: Oxford, 1995; pp 409-431.
    • (1995) Comprehensive Organic Functional Group Transformations , pp. 409-431
    • Qi, H.1    Curran, D.P.2
  • 16
    • 0035828834 scopus 로고    scopus 로고
    • For a review on the synthesis of cyclopropane-containing natural products, see: Donaldson, W. A. Tetrahedron 2001, 57, 8589-8627.
    • (2001) Tetrahedron , vol.57 , pp. 8589-8627
    • Donaldson, W.A.1
  • 17
    • 0037884930 scopus 로고    scopus 로고
    • For reviews on the synthesis of cyclopropane derivatives, see: (a) Reissig, H.-U.; Zimmer, R. Chem. Rev. 2003, 103, 1151-1196.
    • (2003) Chem. Rev. , vol.103 , pp. 1151-1196
    • Reissig, H.-U.1    Zimmer, R.2
  • 24
    • 33646451758 scopus 로고    scopus 로고
    • note
    • The use of lithium and sodium enolates resulted in recovery of the starting material and a lower yield of 14, respectively.
  • 26
    • 33646458460 scopus 로고    scopus 로고
    • note
    • The relative stereochemistry was not determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.