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Volumn 3, Issue 8, 1997, Pages 1299-1314

Achiral cycledextrin analogues

Author keywords

Analogues; Carbohydrates; Cyclodextrin; Cyclooligomerizations; Glycosylations; Nan ostructures

Indexed keywords


EID: 0030794768     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.19970030818     Document Type: Article
Times cited : (38)

References (71)
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    • a) W. Saenger, in Inclusion Compounds, Vol. 2 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol), Academic Press, London, 1984, pp. 231-259;
    • (1984) Inclusion Compounds , vol.2 , pp. 231-259
    • Saenger, W.1
  • 2
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    • (Ed.: D. Duchêne), Editions de Santé, Paris
    • b) Cyclodextrins and Their Industrial Uses (Ed.: D. Duchêne), Editions de Santé, Paris, 1987;
    • (1987) Cyclodextrins and Their Industrial Uses
  • 33
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    • Toshima, K.1    Tatsuta, K.2
  • 37
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    • For a discussion of the CED method of glycosylation, see: N. K. Kochetkov, Tetrahedron 1987, 43, 2389-2436 and references cited therein.
    • (1987) Tetrahedron , vol.43 , pp. 2389-2436
    • Kochetkov, N.K.1
  • 51
    • 0000863666 scopus 로고
    • 4/collidine. See: a) N. K. Kochetkov, N. E. Byramova, Y. E. Tsvetkov, L. V. Backinowsky, Tetrahedron 1985, 41, 3363-3375; b) N. K. Kochetkov, N. E. Nifant'ev, L. V. Backinowsky, ibid. 1987, 43, 3109-3121; c) Y. E. Tsvetkov, L. V. Backinowsky, N. K. Kochetkov. Carbohydr. Res. 1989, 193, 75-90.
    • (1985) Tetrahedron , vol.41 , pp. 3363-3375
    • Kochetkov, N.K.1    Byramova, N.E.2    Tsvetkov, Y.E.3    Backinowsky, L.V.4
  • 52
    • 0000361816 scopus 로고
    • 4/collidine. See: a) N. K. Kochetkov, N. E. Byramova, Y. E. Tsvetkov, L. V. Backinowsky, Tetrahedron 1985, 41, 3363-3375; b) N. K. Kochetkov, N. E. Nifant'ev, L. V. Backinowsky, ibid. 1987, 43, 3109-3121; c) Y. E. Tsvetkov, L. V. Backinowsky, N. K. Kochetkov. Carbohydr. Res. 1989, 193, 75-90.
    • (1987) Tetrahedron , vol.43 , pp. 3109-3121
    • Kochetkov, N.K.1    Nifant'ev, N.E.2    Backinowsky, L.V.3
  • 53
    • 0024982115 scopus 로고
    • 4/collidine. See: a) N. K. Kochetkov, N. E. Byramova, Y. E. Tsvetkov, L. V. Backinowsky, Tetrahedron 1985, 41, 3363-3375; b) N. K. Kochetkov, N. E. Nifant'ev, L. V. Backinowsky, ibid. 1987, 43, 3109-3121; c) Y. E. Tsvetkov, L. V. Backinowsky, N. K. Kochetkov. Carbohydr. Res. 1989, 193, 75-90.
    • (1989) Carbohydr. Res. , vol.193 , pp. 75-90
    • Tsvetkov, Y.E.1    Backinowsky, L.V.2    Kochetkov, N.K.3
  • 59
    • 0343758427 scopus 로고    scopus 로고
    • note
    • Attempts to employ normal-phase preparative HPLC for separation of cyclic oligosaccharides larger than the octamer were unsuccessful.
  • 61
    • 0342453118 scopus 로고    scopus 로고
    • note
    • 4-catalyzed poly-condensation leading to acylated (1 → 4)-α-D-mannan and α-L-rhamnan respectively. See ref. [18].
  • 62
    • 0342453117 scopus 로고    scopus 로고
    • note
    • Each of the achiral molecules 20-24 and 28 incorporates 5n chiral centres, where n is the number of monosaccharide constituents.
  • 67
    • 0000046916 scopus 로고    scopus 로고
    • (Eds.: J. Szejtli, T. Osa), Elsevier, Oxford
    • The use of a number of mass spectrometric techniques for the characterization of CD inclusion complexes has been reported over the years. See: L. Szente, in Comprehensive Supramolecular Chemistry, Vol. 3 (Eds.: J. Szejtli, T. Osa), Elsevier, Oxford, 1996, pp. 253-278, and references cited therein.
    • (1996) Comprehensive Supramolecular Chemistry , vol.3 , pp. 253-278
    • Szente, L.1
  • 71
    • 0343758425 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100129. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: int. code +(1223)336-033; e-mail: deposit@chemcrys.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.