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Volumn 51, Issue 52, 2010, Pages 6890-6892

Efficient oxidation-Wittig olefination-Diels-Alder multicomponent reactions of α-hydroxyketones

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE DERIVATIVE; KETOL;

EID: 78650677199     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.10.121     Document Type: Article
Times cited : (18)

References (67)
  • 24
    • 0012815011 scopus 로고    scopus 로고
    • For the application of intermolecular hetero Diels-Alder reactions in MCR sequences
    • (g) Powell, D. A.; Batey, R. A. Org. Lett. 2002, 4, 2913-2916
    • (2002) Org. Lett. , vol.4 , pp. 2913-2916
    • Powell, D.A.1    Batey, R.A.2
  • 59
    • 85030578129 scopus 로고    scopus 로고
    • note
    • + 143.0704.
  • 60
    • 61349084801 scopus 로고    scopus 로고
    • 2 cannot at this time be ruled out. Studies to clarify this point and to assess the potential of Lewis acid catalysis of the cycloaddition step are ongoing. For studies on the beneficial role of silica on Diels-Alder reactions
    • 2 cannot at this time be ruled out. Studies to clarify this point and to assess the potential of Lewis acid catalysis of the cycloaddition step are ongoing. For studies on the beneficial role of silica on Diels-Alder reactions, see: (a) Cunningham, I. D.; Crawley, V. J. Mol. Catal. A 2009, 301, 47-51;
    • (2009) J. Mol. Catal. A , vol.301 , pp. 47-51
    • Cunningham, I.D.1    Crawley, V.2
  • 63
    • 25144436523 scopus 로고    scopus 로고
    • For Cr(III) and Mn(II) catalysed Diels-Alder cycloadditions see
    • For Cr(III) and Mn(II) catalysed Diels-Alder cycloadditions see: (d) Jarvo, E. R.; Lawrence, B. M.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2005, 44, 6043-6046;
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6043-6046
    • Jarvo, E.R.1    Lawrence, B.M.2    Jacobsen, E.N.3
  • 65
    • 85030587412 scopus 로고    scopus 로고
    • note
    • + 225.1484.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.