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Veschambre Henri
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http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_22/101021jo00231a013/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_1/101021jo00201a025/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_7/101021jo001480f/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_22/101021jo00257a004/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_11/101021jo00037a044/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1994/volume_59/issue_26/101021jo00105a060/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_2/101021jo00378a017/authorship/5
http://hub.abes.fr/springer/periodical/11224/1995/volume_6/issue_3/B937B7D09FAF5EAFE053120B220A9FCB/authorship/6
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Enantioselective Synthesis of Both Enantiomers of Cathinone via the Microbiological Reduction of 2-Azido-1-phenyl-1-propanone
Use of biological systems for the preparation of chiral molecules. 3. Application in pheromone synthesis: preparation of sulcatol enantiomers
Inducibility of an enone reductase system in the fungus Beauveria sulfurescens: application in enantioselective organic synthesis
Use of biological catalysts for the preparation of chiral molecules. 8. Preparation of propargylic alcohols. Application in the total synthesis of leukotriene B4
Deoxysugars via Microbial Reduction of 5-Acyl-isoxazolines:Application to the Synthesis of 3-Deoxy-d-fructose and Derivatives
Synthesis and structural characterization of camphanates of (−)-(2S3S,3S) and (+)-(2S,3R)-4-Phenyl-3-bromo-2-butanol diastereoisomers
(2R,5R)-(-)-2,5-Dimethylcyclopentanone and (5S)-(+)-2,5-dimethyl-2-cyclopenten-1-one by microbiological reduction of racemic 2,5-dimethyl-2-cyclopenten-1-one
Use of biological systems for the synthesis of chiral molecules. 5. Microbiological reduction of acyclic .beta.-diketones
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