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Volumn 20, Issue 7-8, 2001, Pages 667-680

Synthesis of imino-C-disaccharides related to sucrose

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Indexed keywords


EID: 0035527799     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1081/CAR-100108281     Document Type: Article
Times cited : (5)

References (14)
  • 1
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    • note
    • Dedicated to Prof. Joachim Thiem on the occasion of his 60th birthday.
  • 3
    • 0001925108 scopus 로고    scopus 로고
    • Modified carbohydrates and carbohydrate analogues
    • Boons, G.-J. Ed.; Blackie Academic & Professional: London
    • Nicotra, F. Modified Carbohydrates and Carbohydrate Analogues. In Carbohydrate Chemistry, Boons, G.-J. Ed.; Blackie Academic & Professional: London, 1998; 384.
    • (1998) Carbohydrate Chemistry , pp. 384
    • Nicotra, F.1
  • 4
    • 33845278374 scopus 로고
    • Synthesis of C-sucrose
    • Dyer, U. C.; Kishi, Y. Synthesis of C-Sucrose. J. Org. Chem. 1988, 53 (14), 3383-3384.
    • (1988) J. Org. Chem. , vol.53 , Issue.14 , pp. 3383-3384
    • Dyer, U.C.1    Kishi, Y.2
  • 5
    • 0001522011 scopus 로고
    • Preferred conformation of C-glycosides. 11. C-sucrose: New practical synthesis, structural reassignment, and solid-state and solution conformation of its octaacetate
    • O’Leary, D. J.; Kishi, Y. Preferred Conformation of C-Glycosides. 11. C-Sucrose: New Practical Synthesis, Structural Reassignment, and SoliD-State and Solution Conformation of Its Octaacetate. J. Org. Chem. 1993, 58 (2), 304-306.
    • (1993) J. Org. Chem. , vol.58 , Issue.2 , pp. 304-306
    • O’Leary, D.J.1    Kishi, Y.2
  • 6
    • 37049078759 scopus 로고
    • Synthesis of 1-(α-D-glucopyranosyl)-1-deoxy-D-fructose a non-metabolisable analogue of sucrose
    • Carcano, M; Nicotra, F.; Panza, L.; Russo, G. Synthesis of 1-(α-D-Glucopyranosyl)-1-deoxy-D-fructose a Non-metabolisable Analogue of Sucrose. J. Chem. Soc., Chem. Commun. 1989, 10, 642-643.
    • (1989) J. Chem. Soc., Chem. Commun. , vol.10 , pp. 642-643
    • Carcano, M.1    Nicotra, F.2    Panza, L.3    Russo, G.4
  • 9
    • 85021037731 scopus 로고    scopus 로고
    • note
    • As expected, the Wittig reaction afforded selectively the product with E stereochemistry, no Z isomer was detected by NMR.
  • 10
    • 33748632563 scopus 로고
    • On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical rule
    • Cha, J. K.; Christ, W. J.; Kishi, Y. On Stereochemistry of Osmium Tetraoxide Oxidation of Allylic Alcohol Systems. Empirical Rule. Tetrahedron 1984, 40 (12), 2247-2256.
    • (1984) Tetrahedron , vol.40 , Issue.12 , pp. 2247-2256
    • Cha, J.K.1    Christ, W.J.2    Kishi, Y.3
  • 11
    • 0002557146 scopus 로고
    • Anhydrous iron(III) chloride dispersed on silica gel; III. A convenient and mild reagent for deacetalization in dry medium
    • Fadel, A.; Yefsah, R.; Salaün, J. Anhydrous Iron(III) Chloride Dispersed on Silica Gel; III. A Convenient and Mild Reagent for Deacetalization in Dry Medium. Synthesis 1987, 37-40.
    • (1987) Synthesis , pp. 37-40
    • Fadel, A.1    Yefsah, R.2    Salaün, J.3
  • 12
    • 0000040193 scopus 로고
    • Double asymmetric induction in the osmylation of γ-alkoxy α,β-unsaturated esters
    • Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L. Double Asymmetric Induction in the Osmylation of γ-Alkoxy α,β-Unsaturated Esters. Tetrahedron 1988, 44 (22), 6897-6902.
    • (1988) Tetrahedron , vol.44 , Issue.22 , pp. 6897-6902
    • Annunziata, R.1    Cinquini, M.2    Cozzi, F.3    Raimondi, L.4
  • 14
    • 0001320196 scopus 로고
    • Stereoselective synthesis of α-C-allyl-glycopyranosides
    • Giannis, A.; Sandhoff, K. Stereoselective Synthesis of α-C-Allyl-Glycopyranosides. Tetrahedron Lett. 1985, 26 (12), 1479-1482.
    • (1985) Tetrahedron Lett. , vol.26 , Issue.12 , pp. 1479-1482
    • Giannis, A.1    Sandhoff, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.