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Volumn 9, Issue 10, 2007, Pages 1983-1986

2-Alkenoyl pyridine N-oxides, highly efficient dienophiles for the enantioselective Cu(II)-bis(oxazoline) catalyzed diels - Alder reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; CHALCONE; COPPER; CYCLOPENTANE DERIVATIVE; HETEROCYCLIC COMPOUND; OXAZOLE DERIVATIVE; OXAZOLIDINE; PYRIDINE 1 OXIDE; PYRIDINE DERIVATIVE; PYRIDINE N-OXIDE; UNCLASSIFIED DRUG;

EID: 34249331624     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0705752     Document Type: Article
Times cited : (56)

References (40)
  • 5
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    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin
    • (a) Evans, D. A.; Johnson, J. S. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 3.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3
    • Evans, D.A.1    Johnson, J.S.2
  • 6
    • 0003497902 scopus 로고    scopus 로고
    • Kobayashi, S, Jørgensen, K. A, Eds, Wiley-VCH: New York
    • (b) Cycloaddition Reactions in Organic Synthesis; Kobayashi, S., Jørgensen, K. A., Eds.; Wiley-VCH: New York, 2002.
    • (2002) Cycloaddition Reactions in Organic Synthesis
  • 7
    • 0003441992 scopus 로고    scopus 로고
    • Yamamoto, H, Ed, Wiley-VCH: New York, Vols, and 2
    • (c) Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: New York. 2000; Vols. 1 and 2.
    • (2000) Lewis Acids in Organic Synthesis , vol.1
  • 34
    • 33749828310 scopus 로고    scopus 로고
    • For a review on BOX-catalyzed reactions, see
    • For a review on BOX-catalyzed reactions, see: Desimoni, G.; Faita, G.; Jørgensen, K. A. Chem. Rev. 2006, 106, 3561-3651.
    • (2006) Chem. Rev , vol.106 , pp. 3561-3651
    • Desimoni, G.1    Faita, G.2    Jørgensen, K.A.3
  • 39
    • 34249326639 scopus 로고    scopus 로고
    • No DA reaction took place between the poorly reactive diene furan and compound 4a. Instead, a sluggish Michael addition of furan to enone 4a was observed at room temperature.
    • No DA reaction took place between the poorly reactive diene furan and compound 4a. Instead, a sluggish Michael addition of furan to enone 4a was observed at room temperature.
  • 40
    • 33845550434 scopus 로고
    • Fife, K. F. J. Org. Chem. 1983, 48, 1375-1377.
    • (1983) Org. Chem , vol.48 , pp. 1375-1377
    • Fife, K.F.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.