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Volumn , Issue 2, 2007, Pages 225-236

Synthetic approaches to α,β-unsaturated δ-lactones and lactols

Author keywords

Lactones; Natural products; Total synthesis

Indexed keywords


EID: 33846423513     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600570     Document Type: Short Survey
Times cited : (131)

References (128)
  • 24
    • 0001704941 scopus 로고
    • Diastereoselective HDA reactions between chiral aldehydes and Brassard's diene in the presence of europium Lewis acids have also been described, see
    • Diastereoselective HDA reactions between chiral aldehydes and Brassard's diene in the presence of europium Lewis acids have also been described, see: M. M. Midland, S. R. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296.
    • (1984) J. Am. Chem. Soc , vol.106 , pp. 4294-4296
    • Midland, M.M.1    Graham, S.R.2
  • 27
    • 0029980787 scopus 로고    scopus 로고
    • 3 (2%) and giving a good yield and good diastereoselectivity has also been described, see: T. Bauer, C. Chapuis, A. Jezewski, J. Kozak, J. Jurczak, Tetrahedron: Asymmetry 1996, 1391-1404;
    • 3 (2%) and giving a good yield and good diastereoselectivity has also been described, see: T. Bauer, C. Chapuis, A. Jezewski, J. Kozak, J. Jurczak, Tetrahedron: Asymmetry 1996, 1391-1404;
  • 28
    • 0000948384 scopus 로고
    • For a racemic approach, see
    • b) For a racemic approach, see: M. Chmielewski, J. Jurczak, J. Org. Chem. 1981, 46, 2230-2233.
    • (1981) J. Org. Chem , vol.46 , pp. 2230-2233
    • Chmielewski, M.1    Jurczak, J.2
  • 36
    • 23044486219 scopus 로고    scopus 로고
    • For recent excellent reviews on vinylogous Mukaiyama reactions, see: a
    • For recent excellent reviews on vinylogous Mukaiyama reactions, see: a) S. E. Denmark, J. R. Heemstra, G. L. Beutner, Angew. Chem. Int. Ed. 2005, 44, 4682;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 4682
    • Denmark, S.E.1    Heemstra, J.R.2    Beutner, G.L.3
  • 115
    • 0041529886 scopus 로고    scopus 로고
    • For an alternative Baeyer-Villiger approach affording enantiomerically pure six-membered saturated lactones, see: S. Wang, M. M. Kayser, V. Jurkauskas, J. Org. Chem. 2003, 68, 6222-6228
    • b) For an alternative Baeyer-Villiger approach affording enantiomerically pure six-membered saturated lactones, see: S. Wang, M. M. Kayser, V. Jurkauskas, J. Org. Chem. 2003, 68, 6222-6228.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.