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Volumn 37, Issue 12, 1996, Pages 1991-1994

An efficient synthetic approach to aza-C-glycosyl compounds. Application to the synthesis of an aza-C-disaccharide

Author keywords

[No Author keywords available]

Indexed keywords

DISACCHARIDE; GLYCOSIDE; PIPERIDINE DERIVATIVE;

EID: 0029914515     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00226-2     Document Type: Article
Times cited : (65)

References (33)
  • 4
    • 0040922395 scopus 로고
    • Benjamin: New York
    • Smith, P. A. S. The Chemistry of Open-chain Organic Nitrogen Compounds, Benjamin: New York, 1965. In most α-alkoxyamino compounds, the nitrogen atom is part of an amide, carbamate, or equivalent function. See: Houben-Weyl, Methoden der Organischen Chemie, Bd. E14a/2 (O/N-Acetale), Thieme Verlag: Stuttgart, 1991. For an example derived from an azasugar: Johnson, C. R.; Golebiowski, A.; Sundram, H.; Miller, M. W.; Dwaihy, R. L. Tetrahedron Lett. 1995, 36, 653-654.
    • (1965) The Chemistry of Open-chain Organic Nitrogen Compounds
    • Smith, P.A.S.1
  • 5
    • 0042056844 scopus 로고
    • (O/N-Acetale), Thieme Verlag: Stuttgart
    • Smith, P. A. S. The Chemistry of Open-chain Organic Nitrogen Compounds, Benjamin: New York, 1965. In most α-alkoxyamino compounds, the nitrogen atom is part of an amide, carbamate, or equivalent function. See: Houben-Weyl, Methoden der Organischen Chemie, Bd. E14a/2 (O/N-Acetale), Thieme Verlag: Stuttgart, 1991. For an example derived from an azasugar: Johnson, C. R.; Golebiowski, A.; Sundram, H.; Miller, M. W.; Dwaihy, R. L. Tetrahedron Lett. 1995, 36, 653-654.
    • (1991) Methoden der Organischen Chemie , vol.E14A , Issue.2
    • Houben-Weyl1
  • 6
    • 0028831989 scopus 로고
    • Smith, P. A. S. The Chemistry of Open-chain Organic Nitrogen Compounds, Benjamin: New York, 1965. In most α-alkoxyamino compounds, the nitrogen atom is part of an amide, carbamate, or equivalent function. See: Houben-Weyl, Methoden der Organischen Chemie, Bd. E14a/2 (O/N-Acetale), Thieme Verlag: Stuttgart, 1991. For an example derived from an azasugar: Johnson, C. R.; Golebiowski, A.; Sundram, H.; Miller, M. W.; Dwaihy, R. L. Tetrahedron Lett. 1995, 36, 653-654.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 653-654
    • Johnson, C.R.1    Golebiowski, A.2    Sundram, H.3    Miller, M.W.4    Dwaihy, R.L.5
  • 7
    • 0028242129 scopus 로고
    • An example of azasugar thioglycoside has been reported: Suzuki, K.; Hashimoto, H. Tetrahedron Lett. 1994, 35, 4119-4122.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4119-4122
    • Suzuki, K.1    Hashimoto, H.2
  • 18
    • 85029974097 scopus 로고    scopus 로고
    • note
    • All new compounds were fully characterized by spectral data and microanalysis or mass spectrometry. The configuration of 5-8 was inferred from the structure of the cyclized products 9-12.
  • 20
    • 0023656051 scopus 로고
    • (b) Bernotas, R. C.; Pezzone, M. A.; Ganem, B. Carbohydr. Res. 1987, 167, 305-311. See also: Roussel, P.; Perie, J. J.; Laval, J. P.; Lattes, A. Tetrahedron 1972, 28, 701-716.
    • (1987) Carbohydr. Res. , vol.167 , pp. 305-311
    • Bernotas, R.C.1    Pezzone, M.A.2    Ganem, B.3
  • 21
    • 0041555644 scopus 로고
    • (b) Bernotas, R. C.; Pezzone, M. A.; Ganem, B. Carbohydr. Res. 1987, 167, 305-311. See also: Roussel, P.; Perie, J. J.; Laval, J. P.; Lattes, A. Tetrahedron 1972, 28, 701-716.
    • (1972) Tetrahedron , vol.28 , pp. 701-716
    • Roussel, P.1    Perie, J.J.2    Laval, J.P.3    Lattes, A.4
  • 22
    • 85029985966 scopus 로고    scopus 로고
    • note
    • The alternate epimer could not be detected by NMR spectroscopy.
  • 23
    • 85029980894 scopus 로고    scopus 로고
    • note
    • This is by analogy with the stereochemistry of the internal alkoxymercuration of heptenitols.
  • 26
    • 85029976372 scopus 로고    scopus 로고
    • note
    • 3,4 7.4, H-3).
  • 27
    • 85029976816 scopus 로고    scopus 로고
    • note
    • 4,5 9.5, H-4).
  • 28
    • 85029978597 scopus 로고    scopus 로고
    • note
    • +, 100%).
  • 31
    • 85029996425 scopus 로고    scopus 로고
    • note
    • +, 100%).
  • 33
    • 85029997751 scopus 로고    scopus 로고
    • note
    • 1pro-S,3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.