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Volumn 18, Issue 8, 2007, Pages 931-948

The exo-deoxoanomeric effect in the conformational preferences of C-glycosides

Author keywords

[No Author keywords available]

Indexed keywords

AGLYCONE; CARBON 13; GLYCOSIDE; HYDROGEN; HYDROXYL GROUP; METHYL GROUP;

EID: 34248682389     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.04.007     Document Type: Article
Times cited : (15)

References (63)
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    • Montreuil J., Vliegenthart J.F.G., and Schachter H. (Eds), Elsevier, Amsterdam
    • In: Montreuil J., Vliegenthart J.F.G., and Schachter H. (Eds). Glycoproteins and Disease (1996), Elsevier, Amsterdam
    • (1996) Glycoproteins and Disease
  • 7
    • 34248665119 scopus 로고    scopus 로고
    • Sas, B.; Van der Eycken, J.; Van Hemel, J.; Blom, P.; Vandenkerckhove, J.; Ruttens, B. PCT Int. WO03032905, 2003.
  • 12
    • 0001698493 scopus 로고
    • and references cited therein
    • Kishi Y. Pure Appl. Chem. 65 (1993) 771-778 and references cited therein
    • (1993) Pure Appl. Chem. , vol.65 , pp. 771-778
    • Kishi, Y.1
  • 16
    • 0037025963 scopus 로고    scopus 로고
    • and references cited therein
    • Kishi Y. Tetrahedron 58 (2002) 6239-6258 and references cited therein
    • (2002) Tetrahedron , vol.58 , pp. 6239-6258
    • Kishi, Y.1
  • 28
    • 34248637738 scopus 로고    scopus 로고
    • note
    • The first descriptor indicates the torsional relationship between O6 and O5, and the second that between O6 and C4.
  • 43
    • 34248681705 scopus 로고    scopus 로고
    • note
    • For easier discussion, C-glycosides are numbered here according to semisystematic names generally accepted for this class of compounds.
  • 49
    • 34248633878 scopus 로고    scopus 로고
    • note
    • Note that the R/S descriptors for the prochiral protons at C1′ of the model compounds 11, 13, 14, 18, and 19 have changed, as a consequence of applying the priority rules of the R-S system.
  • 52
    • 34248676148 scopus 로고    scopus 로고
    • note
    • H1,H1′S = 0) was assumed.
  • 53
    • 34248683772 scopus 로고    scopus 로고
    • note
    • The axial configuration at C4 in alkyl galactopyranosides makes the gt and tg more stable rotamers.
  • 57
    • 34248634997 scopus 로고    scopus 로고
    • note
    • 2 are the intensities of the first and second Cotton effects.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.