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Volumn 3, Issue 26, 2001, Pages 4201-4203

Thioglycosides protected as trans-2,3-cyclic carbonates in chemoselective glycosylations

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[No Author keywords available]

Indexed keywords

ARTICLE;

EID: 0043264789     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016869j     Document Type: Article
Times cited : (59)

References (26)
  • 1
    • 0030058793 scopus 로고    scopus 로고
    • For a review on strategies in oligosaccharides synthesis, see: Boons, G.-J. Tetrahedron 1996, 52, 1095.
    • (1996) Tetrahedron , vol.52 , pp. 1095
    • Boons, G.-J.1
  • 13
    • 0035955202 scopus 로고    scopus 로고
    • During the preparation of this manuscript, Kerns et al. reported the use of oxazolidinone protected glucosamine derivatives for the synthesis of α-linked 2-amino glycosides. Benakli, K.; Zha, C.; Kerns, R. J. J. Am. Chem. Soc. 2001, 123, 9461. For examples of using 2,3-cyclic carbonates as glycosyl donors, see: (a) Gorin, P. A.; Perlin, A. S. Can. J. Chem. 1961, 39, 2474.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9461
    • Benakli, K.1    Zha, C.2    Kerns, R.J.3
  • 14
    • 0001023062 scopus 로고
    • During the preparation of this manuscript, Kerns et al. reported the use of oxazolidinone protected glucosamine derivatives for the synthesis of α-linked 2-amino glycosides. Benakli, K.; Zha, C.; Kerns, R. J. J. Am. Chem. Soc. 2001, 123, 9461. For examples of using 2,3-cyclic carbonates as glycosyl donors, see: (a) Gorin, P. A.; Perlin, A. S. Can. J. Chem. 1961, 39, 2474.
    • (1961) Can. J. Chem. , vol.39 , pp. 2474
    • Gorin, P.A.1    Perlin, A.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.