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1. Structural basis for CCR6 modulation by allosteric antagonists

2. Visible Light Photoredox-Catalyzed Decarboxylative Alkylation of 3‑Aryl-Oxetanes and Azetidines via Benzylic Tertiary Radicals and Implications of Benzylic Radical Stability

5. Extended finite-size scaling of synchronized coupled oscillators

6. Nonlinear stability of phase-locked states for the Kuramoto model with finite inertia

11. Visible Light Photoredox-Catalyzed Decarboxylative Alkylation of 3-Aryl-Oxetanes and Azetidines via Benzylic Tertiary Radicals and Implications of Benzylic Radical Stability

12. Modular Synchronization in Complex Network with a Gauge Kuramoto Model

14. Correction to “Automated Nanomole-Scale Reaction Screening toward Benzoate Bioisosteres: A Photocatalyzed Approach to Highly Elaborated Bicyclo[1.1.1]Pentanes”

16. Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin-1

17. Automated Nanomole-Scale Reaction Screening toward Benzoate Bioisosteres: A Photocatalyzed Approach to Highly Elaborated Bicyclo[1.1.1]Pentanes

22. PF-07059013: A Noncovalent Modulator of Hemoglobin for Treatment of Sickle Cell Disease

24. Lithium‐Catalyzed Thiol Alkylation with Tertiary and Secondary Alcohols: Synthesis of 3‐Sulfanyl‐Oxetanes as Bioisosteres

27. Catalytic Friedel‐Crafts Reactions on Saturated Heterocycles and Small Rings for sp3‐sp2 Coupling of Medicinally Relevant Fragments

29. PF-07059013: A Noncovalent Modulator of Hemoglobin for Treatment of Sickle Cell Disease.

31. Discovery of 3-Cyano-N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist

32. Investigating 3,3-diaryloxetanes as potential bioisosteres through matched molecular pair analysisElectronic supplementary information (ESI) available: Spectroscopic data of synthesized compounds, and experimental procedures for ADME data, and table of log Ddata. See DOI: 10.1039/d1md00248a

33. Visible-Light-Initiated Manganese Catalysis for C−H Alkylation of Heteroarenes: Applications and Mechanistic Studies

35. Structure-Based Approach To Identify 5-[4-Hydroxyphenyl]pyrrole-2-carbonitrile Derivatives as Potent and Tissue Selective Androgen Receptor Modulators

36. Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based Drug Design

37. Catalytic Friedel‐Crafts Reactions on Saturated Heterocycles and Small Rings for sp3‐sp2 Coupling of Medicinally Relevant Fragments.

38. Harnessing Oxetane and Azetidine Sulfonyl Fluorides for Opportunities in Drug Discovery

39. Covalent Enzyme Inhibition through Fluorosulfate Modification of a Noncatalytic Serine Residue

47. Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors

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