Tomoya Yukawa
Takeda (Japan)(JP)
Publications by Year
Research Areas
Crystallization and Solubility Studies, X-ray Diffraction in Crystallography, Sulfur-Based Synthesis Techniques, Catalytic C–H Functionalization Methods, Chemical Synthesis and Reactions
Most-Cited Works
- → Nickel-Catalyzed Carbocyanation of Alkynes with Allyl Cyanides(2009)136 cited
- → Allylcyanation of Alkynes: Regio- and Stereoselective Access to Functionalized Di- or Trisubstituted Acrylonitriles(2006)131 cited
- → Nickel/AlMe2Cl-catalysed carbocyanation of alkynes using arylacetonitriles(2009)65 cited
- → Discovery of [cis-3-({(5R)-5-[(7-Fluoro-1,1-dimethyl-2,3-dihydro-1H-inden-5-yl)carbamoyl]-2-methoxy-7,8-dihydro-1,6-naphthyridin-6(5H)-yl}carbonyl)cyclobutyl]acetic Acid (TAK-828F) as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist(2018)62 cited
- → Nickel/Lewis Acid-Catalyzed Carbocyanation of Alkynes Using Acetonitrile and Substituted Acetonitriles(2010)52 cited
- → Utility of Physicochemical Properties for the Prediction of Toxicological Outcomes: Takeda Perspective(2020)51 cited
- → Stannylative Cycloaddition of Enynes Catalyzed by Palladium−Iminophosphine(2004)40 cited
- → Freshly isolated primary human proximal tubule cells as an in vitro model for the detection of renal tubular toxicity(2020)34 cited
- → Uptake of HMG-CoA reductase inhibitor ZD4522 into hepatocytes and distribution into liver and other tissues of the rat(2000)33 cited
- → Design, Synthesis, and Biological Evaluation of Retinoic Acid-Related Orphan Receptor γt (RORγt) Agonist Structure-Based Functionality Switching Approach from In House RORγt Inverse Agonist to RORγt Agonist(2019)24 cited