VIAF

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Leader 00000nz a2200037n 45 0
001 WKP|Q84109238 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000345.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q84109238‏
024 ‎‡a 0000-0002-6144-4022‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q84109238‏
100 0 ‎‡a Zhong Wang‏ ‎‡c researcher (ORCID 0000-0002-6144-4022)‏ ‎‡9 en‏
670 ‎‡a Author's A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy‏
670 ‎‡a Author's An unexpected and significantly lower hydrogen-bond-donating capacity of fluorohydrins compared to nonfluorinated alcohols.‏
670 ‎‡a Author's Design of fluorinated 5-HT‏
670 ‎‡a Author's Design of fluorinated 5-HT(4)R antagonists: influence of the basicity and lipophilicity toward the 5-HT(4)R binding affinities‏
670 ‎‡a Author's Intramolecular OH⋅⋅⋅Fluorine Hydrogen Bonding in Saturated, Acyclic Fluorohydrins: The γ-Fluoropropanol Motif.‏
670 ‎‡a Author's Reducing the lipophilicity of perfluoroalkyl groups by CF2-F/CF2-Me or CF3/CH3 exchange‏
670 ‎‡a Author's Synthesis of 2,3,4-Trideoxy-2,3,4-trifluoroglucose‏
670 ‎‡a Author's Systematic Investigation of Lipophilicity Modulation by Aliphatic Fluorination Motifs‏
909 ‎‡a (orcid) 0000000261444022‏ ‎‡9 1‏
919 ‎‡a systematicinvestigationoflipophilicitymodulationbyaliphaticfluorinationmotifs‏ ‎‡A Systematic Investigation of Lipophilicity Modulation by Aliphatic Fluorination Motifs‏ ‎‡9 1‏
919 ‎‡a newstraightforwardmethodforlipophilicitylogpmeasurementusing19fnmrspectroscopy‏ ‎‡A A New Straightforward Method for Lipophilicity (logP) Measurement using 19F NMR Spectroscopy‏ ‎‡9 1‏
919 ‎‡a unexpectedandsignificantlylowerhydrogenbonddonatingcapacityoffluorohydrinscomparedtononfluorinatedalcohols‏ ‎‡A An unexpected and significantly lower hydrogen-bond-donating capacity of fluorohydrins compared to nonfluorinated alcohols.‏ ‎‡9 1‏
919 ‎‡a designoffluorinated5ht‏ ‎‡A Design of fluorinated 5-HT‏ ‎‡9 1‏
919 ‎‡a designoffluorinated5ht4rantagonistsinfluenceofthebasicityandlipophilicitytowardthe5ht4rbindingaffinities‏ ‎‡A Design of fluorinated 5-HT(4)R antagonists: influence of the basicity and lipophilicity toward the 5-HT(4)R binding affinities‏ ‎‡9 1‏
919 ‎‡a intramolecular5fluorinehydrogenbondinginsaturatedacyclicfluorohydrinstheγfluoropropanolmotif‏ ‎‡A Intramolecular OH⋅⋅⋅Fluorine Hydrogen Bonding in Saturated, Acyclic Fluorohydrins: The γ-Fluoropropanol Motif.‏ ‎‡9 1‏
919 ‎‡a reducingthelipophilicityofperfluoroalkylgroupsbycf2fcf2meorcf3ch3exchange‏ ‎‡A Reducing the lipophilicity of perfluoroalkyl groups by CF2-F/CF2-Me or CF3/CH3 exchange‏ ‎‡9 1‏
919 ‎‡a synthesisof234trideoxy234trifluoroglucose‏ ‎‡A Synthesis of 2,3,4-Trideoxy-2,3,4-trifluoroglucose‏ ‎‡9 1‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏