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@ARTICLE{Bode:52117,
      author       = {Bode, S. and Wolberg, M. and Müller, M.},
      title        = {{S}tereoselective {S}ynthesis of 1,3-diols},
      journal      = {Synthesis},
      issn         = {0039-7881},
      address      = {Stuttgart [u.a.]},
      publisher    = {Thieme},
      reportid     = {PreJuSER-52117},
      pages        = {557 - 588},
      year         = {2006},
      note         = {Record converted from VDB: 12.11.2012},
      abstract     = {Many polyketide-derived natural products contain a synor
                      anti-1,3-diol unit. No general and simple approach exists
                      for the flexible synthesis of polyols and other
                      polyketide-derived structural units, therefore a multitude
                      of methods for the stereoselective synthesis of 1,3-diols
                      has been developed. Asymmetric homogeneous and heterogeneous
                      hydrogenation and diastereoselective reduction, chain
                      elongation, enzymatic and nonenzymatic desymmetrization, or
                      dynamic kinetic resolution are some of these methods. The
                      development of different methods to synthesize these
                      1,3-diols stereoselectively is important, as often small
                      structural changes in a molecule result in low yields or low
                      stereoselectivity with a known method. This review article
                      highlights some of the recent developments in this field.},
      keywords     = {J (WoSType)},
      cin          = {IBT-2},
      ddc          = {540},
      cid          = {I:(DE-Juel1)VDB56},
      pnm          = {Biotechnologie},
      pid          = {G:(DE-Juel1)FUEK410},
      shelfmark    = {Chemistry, Organic},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000235670600001},
      doi          = {10.1055/s-2006-926315},
      url          = {https://juser.fz-juelich.de/record/52117},
}