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Volumn , Issue 21, 2010, Pages 4062-4074

A urea-linked glucosamine dimer as a building block for the synthesis of linear and cyclic neosaccharides

Author keywords

Carbohydrates; Glycoconjugates; Macrocycles; Oligosaccharides; Reaction mechanisms

Indexed keywords


EID: 77954705978     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000292     Document Type: Article
Times cited : (4)

References (66)
  • 2
    • 35748936397 scopus 로고    scopus 로고
    • State of the art, see: (special issue on Glycomimetics)
    • State of the art, see: Carbohydr. Res. 2007, 342, 1537-1982 (special issue on Glycomimetics).
    • (2007) Carbohydr. Res. , vol.342 , pp. 1537-1982
  • 21
    • 35748933552 scopus 로고    scopus 로고
    • and references cited therein
    • T. Akhtar, I. Cumpstey, Tetrahedron Lett. 2007, 48, 8673-8677, and references cited therein.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 8673-8677
    • Akhtar, T.1    Cumpstey, I.2
  • 43
    • 77954710683 scopus 로고    scopus 로고
    • Compound 11 was obtained by reacting 3 with DMAP and excess NPCC in DMF at 5 °C
    • Compound 11 was obtained by reacting 3 with DMAP and excess NPCC in DMF at 5 °C
  • 65
    • 79960698472 scopus 로고
    • Water suppression was achieved by using excitation sculpting with gradients. For details, see
    • Water suppression was achieved by using excitation sculpting with gradients. For details, see: T. L. Hwang, A. J. Shaka, Magn. Res. A 1995, 112, 275-279.
    • (1995) Magn. Res. A , vol.112 , pp. 275-279
    • Hwang, T.L.1    Shaka, A.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.