@article{SchmidtNave2006,
  author    = {Schmidt, Bernd and Nave, Stefan},
  title     = {Stereoselective syntheses of enantiomerically pure 2,5-disubstituted dihydropyrans based on olefin metathesis},
  series = {The journal of organic chemistry},
  volume    = {71},
  journal   = {The journal of organic chemistry},
  number    = {19},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/jo061190k},
  pages     = {7364 -- 7369},
  year      = {2006},
  abstract  = {A short synthesis of 2,5-disubstituted dihydropyrans starting from D-mannitol as a chiral building block is described. Our synthetic approach combines ruthenium-catalyzed ring closing olefin metathesis and palladium-catalyzed nucleophilic substitution.},
  language  = {en}
}
@article{SchmidtNave2006,
  author    = {Schmidt, Bernd and Nave, Stefan},
  title     = {Palladium-catalyzed O-allylation of alpha-hydroxy carbonyl compounds},
  doi       = {10.1002/adsc.200505361},
  year      = {2006},
  abstract  = {alpha-Hydroxy carbonyl compounds undergo smooth O-allylation using allylic carbonates and Pd(0) catalysts. This method has significant advantages over other O-allylation methods as it provides a solution to several problems previously observed for this synthetic transformation},
  language  = {en}
}
@article{SchmidtNave2006,
  author    = {Schmidt, Bernd and Nave, Stefan},
  title     = {Control of ring size selectivity by substrate directable RCM},
  doi       = {10.1039/B604359c},
  year      = {2006},
  abstract  = {Hydroxy groups may exert strong catalyst-directing effects in olefin metathesis reactions, which are exploited for a ring size-selective RCM reaction},
  language  = {en}
}