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Volumn 40, Issue 25, 1999, Pages 4665-4668

Syntheses of spacer-linked neodisaccharides derived from L-Daunosamine

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE DERIVATIVE; DAUNOSAMINE; DAUNOSAMINE DERIVATIVE; DISACCHARIDE;

EID: 0033580860     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00862-X     Document Type: Article
Times cited : (19)

References (35)
  • 8
    • 0026553306 scopus 로고
    • (c) Nicolaou, K. C.; Schreiner, E. P.; Iwabuchi, Y.; Suzuki, T., Angew. Chem. 1992, 104, 317-319; Angew. Chem. Int. Ed. Engl. 1992, 31, 340-341;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 340-341
  • 11
    • 0030502608 scopus 로고    scopus 로고
    • (e) Depew, K. M.; Zeman, S. M.; Boyer, S. H.; Denhart, D. J.; Ikemoto, N.; Danishefsky, S. J.; Crothers, D. M., Angew. Chem. 1996, 108, 2972-2975; Angew. Chem. Int. Ed Engl. 1996, 35, 2797-2801.
    • (1996) Angew. Chem. Int. Ed Engl. , vol.35 , pp. 2797-2801
  • 13
    • 0032556498 scopus 로고    scopus 로고
    • 4. For some examples on the preparation of spacer modified disaccharides refer to: (a) Dominique, R.; Das, S. K.; Roy, R., Chem. Comm. 1998, 2437-2438;
    • (1998) Chem. Comm. , pp. 2437-2438
    • Dominique, R.1    Das, S.K.2    Roy, R.3
  • 21
    • 0000063152 scopus 로고    scopus 로고
    • (c) Schuster, M.; Blechert, S., Angew. Chem. 1997, 108, 2124-2144; Angew. Chem. Int. Ed. Engl. 1997, 36, 2036-2055;
    • (1997) Angew. Chem. , vol.108 , pp. 2124-2144
    • Schuster, M.1    Blechert, S.2
  • 22
    • 0030771019 scopus 로고    scopus 로고
    • (c) Schuster, M.; Blechert, S., Angew. Chem. 1997, 108, 2124-2144; Angew. Chem. Int. Ed. Engl. 1997, 36, 2036-2055;
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 2036-2055
  • 29
    • 85069277320 scopus 로고    scopus 로고
    • note
    • 9. The sequence can be reversed with reduced overall yield by starting with the 4-O-acylation followed by acid promoted acetal hydrolysis and finally with 1-O-silylation.
  • 31
    • 85069275714 scopus 로고    scopus 로고
    • note
    • 11. 1,4-Butanediol was less useful as glycosyl acceptor in the glycosylation of 5.
  • 32
    • 85069284344 scopus 로고    scopus 로고
    • note
    • 13C NMR δ 170.5 (s), 96.7 (d), 68.7 (d), 66.8 (t), 65.8 (d), 45.3 (d), 29.4 (t), 26.2 (t), 22.4 (q), 16.3 (q).
  • 33
    • 85069280102 scopus 로고    scopus 로고
    • note
    • 13. The dimerizations commonly furnished small amounts of cross-metathesis products obtained from the initially released styrene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.