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http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_1/101021jm990436t/authorship/9
http://hub.abes.fr/acs/periodical/inocaj/2006/volume_45/issue_8/101021ic052104m/authorship/5
http://hub.abes.fr/acs/periodical/inocaj/2007/volume_46/issue_24/101021ic701608x/authorship/5
http://hub.abes.fr/acs/periodical/inocaj/2008/volume_47/issue_16/101021ic800789x/authorship/6
http://hub.abes.fr/acs/periodical/orgnd7/2007/volume_26/issue_12/101021om070200k/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_26/101021jm0708228/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_22/101021jo981150j/authorship/8
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_4/101021jo0352629/authorship/4
http://hub.abes.fr/acs/periodical/orgnd7/2008/volume_27/issue_23/101021om800738r/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_4/101021jm001035c/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_21/101021jo9812375/authorship/3
http://hub.abes.fr/acs/periodical/orgnd7/2007/volume_26/issue_16/101021om070083t/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_1/101021jm9504969/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_7/101021jm950893j/authorship/1
http://hub.abes.fr/acs/periodical/orgnd7/2008/volume_27/issue_15/101021om800299j/authorship/7
http://hub.abes.fr/acs/periodical/orgnd7/2008/volume_27/issue_4/101021om7011198/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_7/101021jo001167d/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_12/101021jo991932s/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_7/101021jo0525985/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_18/101021jm00018a010/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37/issue_20/101021jm00046a011/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_23/101021jm00075a021/authorship/1
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The Squalestatins: Synthesis and Biological Activity of Some C3-Modified Analogs; Replacement of a Carboxylic Acid or Methyl Ester with an Isoelectronic Heterocyclic Functionality
The Squalestatins: Novel Inhibitors of Squalene Synthase. Enzyme Inhibitory Activities and in vivo Evaluation of C1-Modified Analogs
Selective Plasma Hydrolysis ofGlucocorticoid γ-Lactones and CyclicCarbonates by the Enzyme Paraoxonase:An Ideal Plasma Inactivation Mechanism
Synthesis and Characterization of Coronanes: Multicyclopropane-Fused Macrocyclic Arrays
Helical Structure of Tercyclopropanedimethanol in Solution
Heavier Group 2 Element Catalyzed Hydrophosphination of Carbodiimides
The Squalestatins: Inhibitors of Squalene Synthase. Enzyme InhibitoryActivities and inVivo Evaluation of C3-Modified Analogues
Synthesis, Characterization, and Solution Lability of N-Heterocyclic Carbene Adducts of the Heavier Group 2 Bis(trimethylsilyl)amides
4-Acyl-1-(4-aminoalkoxyphenyl)-2-ketopiperazines as a Novel Class of Non-Brain-Penetrant Histamine H3 Receptor Antagonists
Rapid Entry into Mono-, Bi-, and Tricyclic β-Lactam Arrays viaAlkene Metathesis
Bis(diphenylphosphido) Derivatives of the Heavier Group 2 Elements
Reactions of β-Diketiminate-Stabilized Calcium Amides with9-Borabicyclo[3.3.1]nonane (9-BBN)
Rearrangement of a16α,17α-Epoxy-16β-methylandrostane-17β-carbothioic Acid to a17β-Mercapto-16β-methylandrostane-17α,16α-carbolactone
Novel Glucocorticoid Antedrugs Possessing a 17β-(γ-Lactone) Ring
The Squalestatins: Decarboxy and 4-Deoxy Analogues as Potent SqualeneSynthase Inhibitors
Imino Sulfinamidines: Synthesis and Coordination Chemistry of a NovelClass of Chiral Bidentate Ligands
Tandem Ireland−Claisen Rearrangement Ring-Closing AlkeneMetathesis in the Construction of Bicyclic β-Lactam CarboxylicEsters
Calcium-Catalyzed Intermolecular Hydrophosphination
β-Diketiminato Calcium Acetylides: Synthesis, Solution Dimerization, and Catalytic Carbon−Carbon Bond Formation
Synthesis of Diverse Macrocyclic Peptidomimetics UtilizingRing-Closing Metathesis and Solid-Phase Synthesis
Triazenide Complexes of the Heavier Alkaline Earths: Synthesis, Characterization, And Suitability for Hydroamination Catalysis
Inhibitors of cholesterol biosynthesis. 2. 3,5-Dihydroxy-7-(N-pyrrolyl)-6-heptenoates, a novel series of HMG-CoA reductase inhibitors
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