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Volumn 11, Issue 21, 2009, Pages 4998-5001

Enantioselective synthesis of 5-epi-citreoviral using ruthenium-catalyzed asymmetric ring-closing metathesis

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EID: 70350660793     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901853t     Document Type: Article
Times cited : (19)

References (38)
  • 3
    • 70350683743 scopus 로고    scopus 로고
    • Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, Germany, Chapter 2.3
    • (b) Hoveyda, A. H. In Handbook of Metathesis; Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, Germany, 2003; Chapter 2.3.
    • (2003) Handbook of Metathesis
    • Hoveyda, A.H.1
  • 32
    • 0001502234 scopus 로고    scopus 로고
    • Yao, Q. Org. Lett. 2001, 3, 2069-2072.
    • (2001) Org. Lett. , vol.3 , pp. 2069-2072
    • Yao, Q.1
  • 36
    • 70350664627 scopus 로고    scopus 로고
    • 1H NMR spectrum, see the Supporting Information
    • 1H NMR spectrum, see the Supporting Information.
  • 37
    • 0026628175 scopus 로고
    • For another example of an acid-catalyzed ring-opening of a bisepoxide in the synthesis of citreoviral and its stereoisomers see: Ebenezer, W.; Pattenden, G. Tetrahedron Lett. 1992, 33, 4053-4056.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4053-4056
    • Ebenezer, W.1    Pattenden, G.2
  • 38
    • 70350668800 scopus 로고    scopus 로고
    • Attempts to improve the yield of the last step by using procedures known to selectively oxidize a primary alcohol in the presence of a secondary alcohol were unsuccessful
    • Attempts to improve the yield of the last step by using procedures known to selectively oxidize a primary alcohol in the presence of a secondary alcohol were unsuccessful.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.