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Volumn , Issue 12, 1998, Pages 1420-1422

A highly stereoselective construction of glycosyl-β-(1→4)-galactoside linkages by reductive cleavage of cyclic orthoesters

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EID: 0003306743     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-1986     Document Type: Article
Times cited : (18)

References (34)
  • 20
    • 84990168709 scopus 로고
    • β-Mannoside formation via an inversion of configuration at C-2 by a nucleophilic substitution: (h) Kunz, H.; Günther, W. Angew. Chem., Int. Ed. Engl. 1988, 27, 1086.
    • (1988) Angew. Chem., Int. Ed. Engl. , vol.27 , pp. 1086
    • Kunz, H.1    Günther, W.2
  • 23
    • 0001694615 scopus 로고
    • β-Mannoside formation by stereoselective reductions of 2-keto-β-glucoside: (k) Liu, K. K.-C.; Danishefsky, S. J. J. Org. Chem. 1994, 59, 1892;
    • (1994) J. Org. Chem. , vol.59 , pp. 1892
    • Liu, K.K.-C.1    Danishefsky, S.J.2
  • 25
    • 0030978561 scopus 로고    scopus 로고
    • β-Mannoside formation using 1,2-O-cis-stannylene acetals: (m) Hodosi, G.; Kovác, P. J. Am. Chem. Soc. 1997, 119, 2335.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2335
    • Hodosi, G.1    Kovác, P.2
  • 26
  • 30
    • 0043162336 scopus 로고
    • Monte-Carlo conformational searches § were performed using MacroModel 4.5 † with the MM2 * derivative of the MM2 forcefield. § Cheng, G.; Guida, W. C.; Still, W. C. J. Am. Chem. Soc. 1989, 111, 4379.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4379
    • Cheng, G.1    Guida, W.C.2    Still, W.C.3
  • 33
    • 26844454715 scopus 로고    scopus 로고
    • note
    • 13C-Chemical shifts (δ in ppm relative to TMS) of anomeric carbons (C-1, C-1′): 3a: 98.1, 103.8, 3b: 98.3, 104.4.
  • 34
    • 26844467915 scopus 로고    scopus 로고
    • note
    • 13C-Chemical shifts (δ in ppm relative to TMS) of anomeric carbons (C-1, C-1′): 2c: 98.7, 100.8, 3c: 97.4, 101.8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.