@article{taid.holmes.at:journals/tetasy/Alzheimer,
  title     = {Synthesis of anti-Alzheimer (R)-arundic acid},
  author    = {Béatrice Pelotier and
               Ta'id Holmes and
               Olivier Piva},
  journal   = {Tetrahedron: Asymmetry},
  publisher = {Elsevier Science},
  year      = {18 April 2005},
  volume    = {16},
  number    = {8},
  pages     = {1513-1520},
  issn      = {0957-4166},
  doi       = {10.1016/j.tetasy.2005.02.011},
  ee        = {http://dx.doi.org/10.1016/j.tetasy.2005.02.011},
  abstract  = {The asymmetric synthesis of the anti-Alzheimer agent (R)-arundic acid has been performed via a diastereoselective photodeconjugation reaction as the key-step. The synthetic approach involves a readily available chiral auxiliary, diacetone-d-glucose, and allows access to either enantiomer as illustrated by the synthesis of (S)-arundic acid. Both enantiomers were obtained in 88% ee using the same chiral auxiliary.},
  bibsource = {http://research.taid.holmes.at/publications/journals/tetasy/Alzheimer.bib},
}