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Volumn 62, Issue 52, 2006, Pages 12227-12236

1,3-Dipolar cycloaddition of α-alkoxycarbonylnitrones with vinyl ethers and allyl alcohols in the presence of Eu(fod)3: selective activation of (Z)-isomers of the nitrones

Author keywords

Alkoxycarbonylnitrones; 1,3 Dipolar cycloaddition; Europium; Stereoselective; Vinyl ethers

Indexed keywords

ALLYL ALCOHOL; ETHER DERIVATIVE; NITRONE DERIVATIVE; VINYL DERIVATIVE;

EID: 33750962025     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.10.014     Document Type: Article
Times cited : (19)

References (92)
  • 1
    • 33750930824 scopus 로고    scopus 로고
    • For general reviews on cycloadditions of nitrones, see:
  • 8
    • 33750959012 scopus 로고    scopus 로고
    • For recent examples on cycloadditions of α-alkoxycarbonylnitrones, see:
  • 20
    • 33750947272 scopus 로고    scopus 로고
    • For intermolecular cycloaddition of six-membered ring lactone-type nitrones, see:
  • 36
    • 33750937079 scopus 로고    scopus 로고
    • For cycloaddition of six-membered ring lactam-type nitrones, see:
  • 42
    • 33750956536 scopus 로고    scopus 로고
    • For cycloaddition of five-membered ring lactone-type nitrones, see:
  • 47
    • 33750953577 scopus 로고    scopus 로고
    • For five-membered ring lactam-type nitrones, see:
  • 52
    • 33750932909 scopus 로고    scopus 로고
    • note
    • The calculations were conducted by using Spartan'04 for Windows.
  • 53
    • 33750955402 scopus 로고    scopus 로고
    • For reviews on Lewis acid catalyzed cycloaddition of nitrones, see:
  • 56
    • 0038798333 scopus 로고    scopus 로고
    • Asymmetric Metal-catalyzed 1,3-Dipolar Cycloaddition Reactions
    • Kobayashi S., and Jørgensen K.A. (Eds), Wiley-VCH, Weinheim
    • Gothelf K.V. Asymmetric Metal-catalyzed 1,3-Dipolar Cycloaddition Reactions. In: Kobayashi S., and Jørgensen K.A. (Eds). Cycloaddition Reactions in Organic Synthesis (2002), Wiley-VCH, Weinheim 211-247
    • (2002) Cycloaddition Reactions in Organic Synthesis , pp. 211-247
    • Gothelf, K.V.1
  • 58
    • 33750951157 scopus 로고    scopus 로고
    • For recent examples on Lewis acid catalyzed cycloaddition of nitrones with vinyl ethers, see:
  • 68
    • 33750943965 scopus 로고    scopus 로고
    • Eu-shift reagents are known to catalyse aldol reaction of α-alkoxy aldehydes with ketene silyl acetals by forming chelate complexes, see:
  • 72
    • 33750939765 scopus 로고    scopus 로고
    • For Diels-Alder reaction using Eu-shift reagents, see:
  • 85
    • 33750955601 scopus 로고    scopus 로고
    • note
    • 3-induced epimerization of an acetal, see Ref. 16c.
  • 86
    • 33750942472 scopus 로고    scopus 로고
    • note
    • 2)=0.0644. Crystallographic data (excluding structural factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 618991. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (e-mail: deposit@ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.