000 01241 a2200349 4500
005 20250517123758.0
264 0 _c20170207
008 201702s 0 0 eng d
022 _a1873-426X
024 7 _a10.1016/j.carres.2016.10.013
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchalli, Michael
245 0 0 _aFrom secondary alcohols to tertiary fluoro substituents: A simple route to hydroxymethyl branched sugars with a fluorine substituent at the branching point.
_h[electronic resource]
260 _bCarbohydrate research
_cDec 2016
300 _a11-19 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAlcohols
_xchemistry
650 0 4 _aCarbohydrates
_xchemistry
650 0 4 _aFluorides
_xchemistry
650 0 4 _aFluorine
_xchemistry
650 0 4 _aMolecular Structure
650 0 4 _aOxidation-Reduction
650 0 4 _aStereoisomerism
700 1 _aThonhofer, Martin
700 1 _aWolfsgruber, Andreas
700 1 _aWeber, Hansjörg
700 1 _aFischer, Roland
700 1 _aSaf, Robert
700 1 _aStütz, Arnold E
773 0 _tCarbohydrate research
_gvol. 436
_gp. 11-19
856 4 0 _uhttps://doi.org/10.1016/j.carres.2016.10.013
_zAvailable from publisher's website
999 _c26590879
_d26590879