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Volumn 60, Issue 35, 2004, Pages 7629-7636

Inverse electron-demand aza-[4+2] cycloaddition reactions of allenamides

Author keywords

1 Azadiene; Allenamides; Aza glycoside; Cycloaddition; Diels Alder; Inverse Demand

Indexed keywords

AMIDE; GLYCOSIDE; HETEROCYCLIC COMPOUND; SOLVENT;

EID: 3843083073     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.05.117     Document Type: Article
Times cited : (48)

References (98)
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    • For earlier documentations of allenamides, see: (d)
    • For earlier documentations of allenamides, see: (d) Dickinson W.B., Lang P.C. Tetrahedron Lett. 8:1967;3035
    • (1967) Tetrahedron Lett. , vol.8 , pp. 3035
    • Dickinson, W.B.1    Lang, P.C.2
  • 9
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    • For recent chemistry using allenamides, see: (a)
    • For recent chemistry using allenamides, see: (a) Achmatowicz M., Hegedus L.S. J. Org. Chem. 69:2004;2229
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    • Achmatowicz, M.1    Hegedus, L.S.2
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    • For papers before 1997, see Ref. 1a.
    • (n) For papers before 1997, see Ref. 1a.
  • 23
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    • For stereoselective oxa-[4+2] cycloaddition reactions of chiral allenamides, see: (a)
    • For stereoselective oxa-[4+2] cycloaddition reactions of chiral allenamides, see: (a) Wei L.-L., Hsung R.P., Xiong H., Mulder J.A., Nkansah N.T. Org. Lett. 1:1999;2145
    • (1999) Org. Lett. , vol.1 , pp. 2145
    • Wei, L.-L.1    Hsung, R.P.2    Xiong, H.3    Mulder, J.A.4    Nkansah, N.T.5
  • 27
    • 1042265448 scopus 로고    scopus 로고
    • For our other studies using chiral allenamides, see: (a)
    • For our other studies using chiral allenamides, see: (a) Rameshkumar C., Hsung R.P. Angew Chem., Int. Ed. 43:2004;615
    • (2004) Angew Chem., Int. Ed. , vol.43 , pp. 615
    • Rameshkumar, C.1    Hsung, R.P.2
  • 46
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    • For cycloadditions using dienamides, see: (f)
    • For cycloadditions using dienamides, see: (f) Campbell A.L., Lenz G.R. Synthesis. 1987;421
    • (1987) Synthesis , pp. 421
    • Campbell, A.L.1    Lenz, G.R.2
  • 47
    • 0035909641 scopus 로고    scopus 로고
    • For recent studies involving enamides, see: (a)
    • For recent studies involving enamides, see: (a) Fuchs J.R., Funk R.L. Org. Lett. 3:2001;3349
    • (2001) Org. Lett. , vol.3 , pp. 3349
    • Fuchs, J.R.1    Funk, R.L.2
  • 51
    • 0028788175 scopus 로고
    • For the only study of epoxidation of achiral enamides, see: (e)
    • For the only study of epoxidation of achiral enamides, see: (e) Adam W., Reinhardt D., Reissig H.-U., Paulini K. Tetrahedron. 51:1995;12257
    • (1995) Tetrahedron , vol.51 , pp. 12257
    • Adam, W.1    Reinhardt, D.2    Reissig, H.-U.3    Paulini, K.4
  • 83
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    • 20, and MS
    • 20, and MS
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    • Sibi's dibenzylidene substituted oxazolidinone can be purchased from Aldrich. For synthesis see: (a)
    • Sibi's dibenzylidene substituted oxazolidinone can be purchased from Aldrich. For synthesis see: (a) Sibi M.P., Deshpande P.K., Ji J.G. Tetrahedron Lett. 1995;8965
    • (1995) Tetrahedron Lett. , pp. 8965
    • Sibi, M.P.1    Deshpande, P.K.2    Ji, J.G.3
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    • For some leading references, see: (a)
    • For some leading references, see: (a) Hintermann T., Seebach D. Helv. Chim. Acta. 81:1998;2093
    • (1998) Helv. Chim. Acta , vol.81 , pp. 2093
    • Hintermann, T.1    Seebach, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.