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Volumn 37, Issue 21, 1996, Pages 3627-3630

A serendipitous synthesis of cyclokojibiose

Author keywords

anomeric effect; cyclooligosaccharide; internal glycosylation; kojibiose; trichloroacetimidate

Indexed keywords

CYCLOKOJIBIOSE; OLIGOSACCHARIDE; UNCLASSIFIED DRUG;

EID: 15844401379     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00653-3     Document Type: Article
Times cited : (9)

References (29)
  • 9
    • 84894519158 scopus 로고
    • These references also contain a uniform nomenclature of cyclic oligosaccharides
    • (b) Immel, S.; Brickmann, J.; Lichtenthaler, F. W. Liebigs Ann. 1995, 929-942. These references also contain a uniform nomenclature of cyclic oligosaccharides.
    • (1995) Liebigs Ann. , pp. 929-942
    • Immel, S.1    Brickmann, J.2    Lichtenthaler, F.W.3
  • 11
    • 0000492601 scopus 로고
    • Houdier, S.; Vottero, P. J. A. Angew. Chem. 1994, 106, 365; Angew. Chem. Int. Ed. Engl. 1994, 33, 355-356.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 355-356
  • 15
    • 85030200708 scopus 로고    scopus 로고
    • note
    • C 91.2 (C-1), 76.4 (C-2), 75.6 (C-5), 74.4 (C-3), 68.8 (C-4), 61.0 (C-6).
  • 18
    • 0001513404 scopus 로고
    • (a) Schmidt, R. R.; Michel, J. Angew. Chem. 1980, 92, 763-764; Angew. Chem. Int. Ed. Engl. 1980, 19, 731-732.
    • (1980) Angew. Chem. , vol.92 , pp. 763-764
    • Schmidt, R.R.1    Michel, J.2
  • 19
    • 84985624827 scopus 로고
    • (a) Schmidt, R. R.; Michel, J. Angew. Chem. 1980, 92, 763-764; Angew. Chem. Int. Ed. Engl. 1980, 19, 731-732.
    • (1980) Angew. Chem. Int. Ed. Engl. , vol.19 , pp. 731-732
  • 23
    • 85030209751 scopus 로고    scopus 로고
    • note
    • Atom numbering is defined in Ref. 11.
  • 24
    • 85030203420 scopus 로고    scopus 로고
    • note
    • This compound was obtained from 3 by successive hydrogenolysis, acetylation, followed by conversions b and c in Scheme 1.
  • 28
    • 85030207217 scopus 로고    scopus 로고
    • note
    • The exo-anomeric effect would require this angle to be ca. -60°. In methyl α-D-glucopyranoside the corresponding angle is, indeed, -54.4° (Ref. 20).
  • 29
    • 0026414072 scopus 로고
    • For a discussion of the stabilizing factors in a related tricyclic saccharide harboring a flexible dioxane moiety, see: Bock, K.; Pedersen, C.; Defaye, J.; Gadelle, A. K. Carbohydr. Res. 1991, 216, 141-148.
    • (1991) Carbohydr. Res. , vol.216 , pp. 141-148
    • Bock, K.1    Pedersen, C.2    Defaye, J.3    Gadelle, A.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.