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Search for "AIDS" in Full Text gives 52 result(s) in Beilstein Journal of Organic Chemistry.

Vinylogous Mukaiyama aldol reactions with 4-oxy-2-trimethylsilyloxypyrroles: relevance to castanospermine synthesis

  • Roger Hunter,
  • Sophie C. M. Rees-Jones and
  • Hong Su

Beilstein J. Org. Chem. 2007, 3, No. 38, doi:10.1186/1860-5397-3-38

Graphical Abstract
  • (Figure 2). The latter is an indolizidine alkaloid that has received significant attention from the synthetic organic community in view of its potent biological activity as an α- and β-glycosidase inhibitor with promising anti-diabetic,[19] anti-cancer,[20] anti-viral [21] and anti-AIDS activity.[22] The
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Published 03 Nov 2007

Synthesis and glycosidase inhibitory activity of new hexa- substituted C8-glycomimetics

  • Olivia Andriuzzi,
  • Christine Gravier-Pelletier,
  • Gildas Bertho,
  • Thierry Prangé and
  • Yves Le Merrer

Beilstein J. Org. Chem. 2005, 1, No. 12, doi:10.1186/1860-5397-1-12

Graphical Abstract
  • as diabetes, cancer and viral infections including AIDS. Thus, inhibition of intestinal α-glucosidases can be used to treat diabetes through the lowering of blood glucose levels, and α-glucosidase inhibitors are being marketed against type 2 (non-insulinodependent mellitus) diabetes (i.e.: Glyset® or
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Published 07 Oct 2005
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