23 results on '"Flegel, Jana"'
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2. The Pseudo‐Natural Product Tafbromin Selectively Targets the TAF1 Bromodomain 2.
3. A highly enantioselective intramolecular 1,3-dipolar cycloaddition yields novel pseudo-natural product inhibitors of the Hedgehog signalling pathway
4. The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation
5. Phenotypic Discovery of Triazolo[1,5-c]quinazolines as a First-In-Class Bone Morphogenetic Protein Amplifier Chemotype
6. Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone
7. The Pseudo‐Natural Product Rhonin Targets RHOGDI
8. Identification and characterization of inhibitors of hedgehog-induced osteoblast differentiation
9. Combination of Pseudo‐Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo‐Sesquiterpenoid Alkaloids
10. Corrigendum: Rh III ‐Catalyzed C−H Activation of Aryl Hydroxamates for the Synthesis of Isoindolinones
11. Asymmetric Synthesis of 3,3′-Piperidinoyl Spirooxindoles and Discovery of Stereospecific Cycloadducts as Novel Hedgehog Pathway Modulators
12. Rh III ‐Catalyzed C−H Activation of Aryl Hydroxamates for the Synthesis of Isoindolinones
13. Discovery of the Hedgehog Pathway Inhibitor Pipinib that Targets PI4KIIIß
14. Unravelling the Synthesis and Chemistry of Stable, Acyclic, and Double‐Deficient 1,3‐Butadienes: An endo ‐Selective Diels–Alder Route to Hedgehog Pathway Inhibitors
15. Furo[3,2‐b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway
16. Asymmetric Synthesis of 3,3′-Piperidinoyl Spirooxindoles and Discovery of Stereospecific Cycloadducts as Novel Hedgehog Pathway Modulators.
17. RhIII‐Catalyzed C−H Activation of Aryl Hydroxamates for the Synthesis of Isoindolinones.
18. Furo[3,2‐b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway
19. Enantioselective Formal C(sp3 )−H Bond Activation in the Synthesis of Bioactive Spiropyrazolone Derivatives
20. C−H Bond Activation for the Synthesis of Heterocyclic Atropisomers Yields Hedgehog Pathway Inhibitors
21. Enantioselective Formal C(sp3)−H Bond Activation in the Synthesis of Bioactive Spiropyrazolone Derivatives.
22. Phenotypic Discovery of Triazolo[1,5-c]quinazolines as a First-In- Class Bone Morphogenetic Protein Amplifier Chemotype
23. Phenotypic Discovery of Triazolo[1,5- c ]quinazolines as a First-In-Class Bone Morphogenetic Protein Amplifier Chemotype.
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