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Humpf Hans-Ulrich
Humpf H.-U.
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http://hub.abes.fr/acs/periodical/jafcau/2003/volume_51/issue_18/101021jf0344338/authorship/3
http://hub.abes.fr/acs/periodical/jafcau/2003/volume_51/issue_18/101021jf030213i/authorship/3
http://hub.abes.fr/bmj/periodical/gut/2010/volume_60/issue_1/B356DBB03805045AE053120B220A35DA/authorship/11
http://hub.abes.fr/acs/periodical/jafcau/2002/volume_50/issue_10/101021jf0115037/authorship/3
http://hub.abes.fr/acs/periodical/jafcau/2005/volume_53/issue_23/101021jf051501c/authorship/4
http://hub.abes.fr/acs/periodical/jafcau/1999/volume_47/issue_12/101021jf990046f/authorship/2
http://hub.abes.fr/acs/periodical/jafcau/2001/volume_49/issue_5/101021jf001429c/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_11/101021jo0000630/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_16/101021jo0003089/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1998/volume_120/issue_43/101021ja981252r/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_1/101021jo991424i/authorship/4
http://hub.abes.fr/acs/periodical/jafcau/2008/volume_56/issue_14/101021jf801296z/authorship/3
http://hub.abes.fr/acs/periodical/jafcau/2007/volume_55/issue_21/101021jf0717283/authorship/3
http://hub.abes.fr/acs/periodical/jafcau/2008/volume_56/issue_13/101021jf800316m/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_17/101021jo010350j/authorship/2
http://hub.abes.fr/acs/periodical/jafcau/2002/volume_50/issue_14/101021jf020023s/authorship/3
http://hub.abes.fr/acs/periodical/jafcau/2008/volume_56/issue_6/101021jf073444o/authorship/5
http://hub.abes.fr/acs/periodical/jafcau/2006/volume_54/issue_17/101021jf061008g/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_24/101021jo010768h/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1995/volume_60/issue_11/101021jo00116a048/authorship/1
http://hub.abes.fr/acs/periodical/jnprdf/1994/volume_57/issue_12/101021np50114a027/authorship/1
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New Monascus Metabolite Isolated from Red Yeast Rice(Angkak, Red Koji)
α Hydroxylation of Carboxylic Acids with Molecular OxygenCatalyzed by the α Oxidase of Peas (Pisum sativum): A NovelBiocatalytic Synthesis of Enantiomerically Pure (R)-2-Hydroxy Acids
Combined Synthetic/CD Strategy for the StereochemicalAssignment of the Tricarballylic Acid Side Chains of Fumonisin B1
Stable Isotope Dilution Analysis of the Fusarium Mycotoxin Zearalenone
Simultaneous Determination of Fumonisin B1 and HydrolyzedFumonisin B1 in Corn Products by Liquid Chromatography/Electrospray Ionization Mass Spectrometry
Determination of N-(Carboxymethyl)fumonisin B1 in CornProducts by Liquid Chromatography/ElectrosprayIonization-Mass Spectrometry
A New One-Step Strategy for the Stereochemical Assignment ofAcyclic 2- and 3-Sulfanyl-1-alkanols Using the CD ExcitonChirality Method
Analysis of Fumonisin B1 in Fusarium proliferatum-InfectedAsparagus Spears and Garlic Bulbs from Germany by LiquidChromatography−Electrospray Ionization Mass Spectrometry
Determination of 12 Type A and B Trichothecenes in Cerealsby Liquid Chromatography−Electrospray Ionization TandemMass Spectrometry
Thermal Degradation of the Fusarium MycotoxinDeoxynivalenol
Deconjugation and Degradation of Flavonol Glycosides by Pig Cecal Microbiota Characterized by Fluorescence in Situ Hybridization (FISH)
Microscale Determination of the Absolute Configuration ofα-Aryl-Substituted Alcohols by the CD Exciton Chirality Method
New Monascus Metabolites with a Pyridine Structure in RedFermented Rice
Enantioselective Epoxidation with Chiral MnIII(salen) Catalysts: Kinetic Resolution of Aryl-Substituted Allylic Alcohols
Bound Fumonisin B1: Analysis of Fumonisin-B1 Glyco andAmino Acid Conjugates by LiquidChromatography−Electrospray Ionization−Tandem MassSpectrometry
Synthesis of Optically Active α-Methylene β-Lactams throughLipase-Catalyzed Kinetic Resolution
Determination of T-2 and HT-2 Toxins in Cereals Including Oats after Immunoaffinity Cleanup by Liquid Chromatography and Fluorescence Detection
Identification and in Vitro Cytotoxicity of Ochratoxin A Degradation Products Formed during Coffee Roasting
Absolute Stereochemistry of Natural 3,4-Dihydroxy-β-ionone Glycosides by the Cd Exciton Chirality Method
Allylic and Homoallylic CD Exciton Chirality: A Sensitive Method for Determining the Absolute Stereochemistry of Natural Products
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