19 results on '"Yamazaki, Yukiyoshi"'
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2. A facile method for converting alcohol to thioether and its application in the synthesis of a novel GPR119 agonist
3. Synthesis of highly deuterium-labeled ( R)-K-13675, PPAR α agonist, for use as an internal standard for low-level quantification of drugs in plasma
4. A practical synthesis of the PPARα agonist, ( R)-K-13675, starting from ( S)-2-hydroxybutyrolactone
5. Multiorgan Systems Study Reveals Igfbp7 as a Suppressor of Gluconeogenesis after Gastric Bypass Surgery
6. A Study into the ADP-Ribosylome of IFN-γ-Stimulated THP-1 Human Macrophage-like Cells Identifies ARTD8/PARP14 and ARTD9/PARP9 ADP-Ribosylation
7. Multiorgan Systems Study Reveals Igfbp7 as a Suppressor of Gluconeogenesis after Gastric Bypass Surgery.
8. Abstract 175: Dynamin-Related Protein 1 Regulates Proteostasis and Proprotein Convertase Subtilisin/Kexin Type 9 Secretion
9. Abstract 19434: The Novel PPARalpha-Selective Agonist K-877 Improves Dyslipidemia, Enhances Reverse Cholesterol Transport and Decreases Inflammation and Atherosclerosis
10. Novel Synthesis of Butyl (S)-2-Hydroxybutanoate, the Key Intermediate of PPARα Agonist (R)-K-13675 from Butyl (2S,3R)-Epoxybutanoate and Butyl (S)-2,3-Epoxypropanoate
11. Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor α agonists
12. ChemInform Abstract: Enantioselective Synthesis of the PPARα Agonist (R)‐K‐13675 via (S)‐2‐Hydroxybutyrolactone.
13. Enantioselective Synthesis of the PPARα Agonist (R)-K-13675 via (S)-2-Hydroxybutyrolactone
14. Lipase-Catalyzed Enantioselective Hydrolysis of Bis(acyloxymethyl) 1,4-Dihydro-3,5-pyridinedicarboxylates Leading to Optically Active Medicines.
15. Asymmetric Synthesis of (R)-Nilvadipine and (S)-NB 818 via Regioselective Bromination of Chiral 1,4-Dihydropyridines as a Key Step and Enzymatic Resolution of Racemic 2-Hydroxymethyl-1,4-dihydropyridine Derivatives.
16. Lipase AH-Catalyzed Asymmetric Synthesis of (S)-(-)-NB 818
17. Lipase-catalyzed enantiosynthesis of (R)- and (S)-2-(Benzyl(phenyl)amino)ethyl 5-(5,5-Dimethyl-2-oxo-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-pyridinecarboxylate (NZ 105).
18. Determination of the Absolute Configuration of Biologically Active (S)-(-)-NB 818 and Its Structural Correlation with the Stereoselectivity of the Channel Blocking Action.
19. Novel Synthesis of Butyl (S)-2-Hydroxybutanoate, the Key Intermediate of PPARα Agonist (R)-K-13675 from Butyl (2S,3R)-Epoxybutanoate and Butyl (S)-2,3-Epoxypropanoate.
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