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Volumn 44, Issue 41, 2005, Pages 6759-6763

1,5-Lactamized sialyl acceptors for various disialoside syntheses: Novel method for the synthesis of glycan portions of Hp-s6 and HLG-2 gangliosides

Author keywords

Gangliosides; Glycosylation; Lactams; Sialic acids

Indexed keywords

CARBOXYLIC ACIDS; COMPLEXATION; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 27444438620     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200501608     Document Type: Article
Times cited : (89)

References (30)
  • 3
    • 0035805264 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1576-1624;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1576-1624
  • 5
    • 0035901660 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1475-1480;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1475-1480
  • 20
    • 27444445889 scopus 로고    scopus 로고
    • See reference [7]
    • Schmidt's group first disclosed the idea of conformational change of the sialyl acceptor to enhance the reactivity of the C8-hydroxy group. They exploited the 1,7-lactonated sialyl acceptor for 8-O-sialylation but obtained mainly β-disialoside. See reference [7].
  • 22
    • 0033583457 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1131-1133.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1131-1133
  • 30
    • 0029588338 scopus 로고
    • Furuhata's group first reported the 8-O-sulfonylation of neuraminic acid. They also confirmed that no migration or cleavage of the sulfonyl group at the C8-hydroxy group had occurred during the full deacylation and saponification process: M. Tanaka, T. Kai, X.-L. Sun, H. Takayanagi, K. Furuhata, Chem. Pharm. Bull. 1995, 43, 2095-2098.
    • (1995) Chem. Pharm. Bull. , vol.43 , pp. 2095-2098
    • Tanaka, M.1    Kai, T.2    Sun, X.-L.3    Takayanagi, H.4    Furuhata, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.