4.5 Article

Synthesis of β-(1→2)-Linked Oligomannosides

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2009, 期 6, 页码 870-888

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200801024

关键词

Carbohydrates; Asymmetric synthesis; Glycosylation; Oligosaccharides; NMR spectroscopy

资金

  1. Finnish Funding Agency for Technology and Innovation, TEKES [40134/06]
  2. Academy of Finland [121335, 122126]
  3. Magnus Ehrnrooth Foundation
  4. National Glycoscience Graduate School
  5. Academy of Finland (AKA) [122126, 121335, 121335, 122126] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

b-(1 -> 2)-Linked oligomannosides constitute an important class of carbohydrate structures located on the cell surface of several Candida species, including C. albicans. As a result of the immunostimulating properties of such compounds, the upscaling of their synthesis is relevant. In this paper, a highly stereoselective synthesis of beta-(1 -> 2)-linked oligomannosides was performed by further development of and modifications to the methodologies described earlier in the literature. In addition to the synthesis of fully deprotected beta-(1 -> 2)-linked mannobiose and mannotriose, some preliminary modifications to the oligosaccharide core, resulting in close analogues with biological potential, are presented. The fully deprotected products form potential targets for screening against C. albicans and may also result in new model structures for vaccine development. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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