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Volumn 9, Issue 22, 2007, Pages 4487-4490

Stereoselective synthesis of 2-deoxy-furanosides from 2,3-anhydro-furanosyl thioglycosides

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EID: 35949004351     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7019108     Document Type: Article
Times cited : (25)

References (41)
  • 2
    • 4143083511 scopus 로고    scopus 로고
    • Antitumor and Antimicrobial Glycoconjugates
    • Fraser-Reid, B, Tatsuta, K, Thiem, J, Eds, Springer-Verlag: Berlin
    • (b) Lindhorst, T. K. Antitumor and Antimicrobial Glycoconjugates. In Glycoscience: Chemistry and Chemical Biology; Fraser-Reid, B., Tatsuta, K., Thiem, J., Eds.; Springer-Verlag: Berlin, 2001; p 2393.
    • (2001) Glycoscience: Chemistry and Chemical Biology , pp. 2393
    • Lindhorst, T.K.1
  • 4
    • 33747036462 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Toshima, K. Carbohydr. Res. 2006, 341, 1282.
    • (2006) Carbohydr. Res , vol.341 , pp. 1282
    • Toshima, K.1
  • 6
    • 84961386963 scopus 로고    scopus 로고
    • Special Problems in Glycosylation Reactions: 2-Deoxy Sugars
    • Ernst, B, Hart, G. W, Sinay, P, Eds, Wiley-VCH Verlag GmbH: Weinheim, Germany
    • (c) Veyrières, A. Special Problems in Glycosylation Reactions: 2-Deoxy Sugars. In Carbohydrates in Chemistry and Biology; Ernst, B., Hart, G. W., Sinay, P., Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany, 2000; p 367.
    • (2000) Carbohydrates in Chemistry and Biology , pp. 367
    • Veyrières, A.1
  • 19
    • 0026543527 scopus 로고    scopus 로고
    • Selected examples: (a) Mereyala, H. B.; Kulkarni, V. R.; Ravi, D.; Sharma, G. V. M.; Rao, B. V.; Reddy, G. B. Tetrahedron 1992, 48, 545.
    • Selected examples: (a) Mereyala, H. B.; Kulkarni, V. R.; Ravi, D.; Sharma, G. V. M.; Rao, B. V.; Reddy, G. B. Tetrahedron 1992, 48, 545.
  • 36
    • 35949001757 scopus 로고    scopus 로고
    • In all cases, J1,2 was less than 2.0 Hz, indicating a trans relationship between the substituents at C1 and C2
    • 1,2 was less than 2.0 Hz, indicating a trans relationship between the substituents at C1 and C2.
  • 37
    • 35948949563 scopus 로고    scopus 로고
    • When the β-thioglycoside was used, no reaction was observed, thus demonstrating the need for a trans relationship between the sulfur and the epoxide moiety
    • When the β-thioglycoside was used, no reaction was observed, thus demonstrating the need for a trans relationship between the sulfur and the epoxide moiety.
  • 41
    • 35948962421 scopus 로고    scopus 로고
    • f's, and separation required acetylation of the mixture followed by chromatography.
    • f's, and separation required acetylation of the mixture followed by chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.