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Volumn 12, Issue 22, 2010, Pages 5346-5349

Cu(II)-catalyzed acylation by thiol esters under neutral conditions: Tandem acylation-wittig reaction leading to a one-pot synthesis of butenolides

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; BUTENOLIDE; COPPER; DRUG DERIVATIVE; ESTER; GAMMA BUTYROLACTONE; THIOL DERIVATIVE;

EID: 78449275169     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102407k     Document Type: Article
Times cited : (72)

References (21)
  • 1
    • 78449303032 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 11
    • 78449300798 scopus 로고    scopus 로고
    • One-pot lactonizations
    • One-pot lactonizations
  • 13
    • 84980140265 scopus 로고
    • Selected multistep-lactonaization using acylation and the Wittig reaction or the Horner-Wadsworth-Emmons reaction under basic conditions, see:;; Tetrahedron 2009, 65, 8091-8098
    • Bestmann, H. J. Angew. Chem., Int. Ed. 1977, 16, 349-364 Selected multistep-lactonaization using acylation and the Wittig reaction or the Horner-Wadsworth-Emmons reaction under basic conditions, see: N. Villalobos, J. L.; Wood, S.; Jeong, C. L.; Benson, S. M.; Zeman, C.; McCarty, M.; Weiss, M. M.; Salcedo, A.; Jenkins, J. Tetrahedron 2009, 65, 8091-8098
    • (1977) Angew. Chem., Int. Ed. , vol.16 , pp. 349-364
    • Bestmann, H.J.1    Villalobos J L, N.2    Wood, S.3    Jeong, C.L.4    Benson, S.M.5    Zeman, C.6    McCarty, M.7    Weiss, M.M.8    Salcedo, A.9    Jenkins, J.10
  • 15
    • 34548410437 scopus 로고    scopus 로고
    • references cited therein For a selected review on synthesis of butenolides:; J. Chem. Soc., Perkin Trans. 1 2002, 2324-2342
    • Krawczyk, E.; Koprowski, M.; Luczak, J. Tetrahedron: Asymmetry 2007, 18, 1780-1787 and references cited therein For a selected review on synthesis of butenolides: Carter, N. B.; Nadany, A. E.; Sweeney, J. B. J. Chem. Soc., Perkin Trans. 1 2002, 2324-2342
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 1780-1787
    • Krawczyk, E.1    Koprowski, M.2    Luczak, J.3    Carter, N.B.4    Nadany, A.E.5    Sweeney, J.B.6
  • 17
    • 50849108562 scopus 로고    scopus 로고
    • Witt, D. Synthesis 2008, 16, 2491-2509
    • (2008) Synthesis , vol.16 , pp. 2491-2509
    • Witt, D.1
  • 18
    • 78449280059 scopus 로고    scopus 로고
    • For X-ray crystal structure analysis of 6, see Supporting Information
    • For X-ray crystal structure analysis of 6, see Supporting Information.
  • 19
    • 78449275294 scopus 로고    scopus 로고
    • Toluene is safer than THF under oxidative conditions. Furthermore, the catalyst turnover number in toluene was fairly better than in THF
    • Toluene is safer than THF under oxidative conditions. Furthermore, the catalyst turnover number in toluene was fairly better than in THF.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.