293 results on '"Qiao, Jennifer X."'
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2. Palladium (II)‐Catalyzed C−H Activation with Bifunctional Ligands: From Curiosity to Industrialization
3. Versatile Copper-Catalyzed γ‑C(sp3)–H Lactonization of Aliphatic Acids.
4. Site-selective tyrosine bioconjugation via photoredox catalysis for native-to-bioorthogonal protein transformation
5. Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)
6. Remote C–H Olefination of Heterocyclic Biaryls Enabled by Reversibly Bound Templates
7. Synthesis of 1,3-Dienes via Ligand-Enabled Sequential Dehydrogenation of Aliphatic Acids
8. Oral Delivery of Highly Lipophilic, Poorly Water-Soluble Drugs: Self-Emulsifying Drug Delivery Systems to Improve Oral Absorption and Enable High-Dose Toxicology Studies of a Cholesteryl Ester Transfer Protein Inhibitor in Preclinical Species
9. Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)
10. Formation of a-chiral centers by asymmetric β-C(sp³)–H arylation, alkenylation, and alkynylation
11. Discovery of N–X anomeric amides as electrophilic halogenation reagents
12. Remote C−H Olefination of Heterocyclic Biaryls Enabled by Reversibly Bound Templates.
13. Ligand-accelerated non-directed CH functionalization of arenes
14. Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials
15. Ligand-Enabled C–H Hydroxylation with Aqueous H2O2 at Room Temperature
16. Ligand‐Enabled β‐C(sp 3 )−H Lactamization of Tosyl‐Protected Aliphatic Amides Using a Practical Oxidant
17. One-Step Synthesis of β-Alkylidene-γ-lactones via Ligand-Enabled β,γ-Dehydrogenation of Aliphatic Acids
18. Ligand-accelerated non-directed C–H functionalization of arenes
19. ASYMMETRIC CATALYSIS: Formation of α-chiral centers by asymmetric β-C(sp3)-H arylation, alkenylation, and alkynylation
20. Synthesis of tertiary carbinamines
21. Ligand Enabled Pd(II)-Catalyzed γ-C(sp3)–H Lactamization of Native Amides
22. Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C–H activation
23. A tautomeric ligand enables directed C‒H hydroxylation with molecular oxygen
24. Ligand‐Enabled β‐C(sp3)−H Lactamization of Tosyl‐Protected Aliphatic Amides Using a Practical Oxidant.
25. Ni-electrocatalytic Csp3–Csp3 doubly decarboxylative coupling.
26. Ligand-Enabled C–H Hydroxylation with Aqueous H2O2at Room Temperature
27. Site-Selective Functionalization of Methionine Residues via Photoredox Catalysis
28. Serine-Selective Bioconjugation
29. Ligand Enabled Pd(II)-Catalyzed γ‑C(sp3)–H Lactamization of Native Amides.
30. Identification of substituted benzothiazole sulfones as potent and selective inhibitors of endothelial lipase
31. meta ‐Selective C−H Arylation of Fluoroarenes and Simple Arenes
32. Pd-Catalyzed γ-C(sp3)–H Fluorination of Free Amines
33. Transient Directing Group Enabled Pd-Catalyzed γ-C(sp3)–H Oxygenation of Alkyl Amines
34. Ligand-Enabled Pd(II)-Catalyzed C(sp3)–H Lactonization Using Molecular Oxygen as Oxidant
35. Iridium(I)-Catalyzed α-C(sp3)–H Alkylation of Saturated Azacycles
36. β ‐Selective C−H Arylation of Electron‐Deficient Thiophenes, Pyrroles, and Furans
37. Corrigendum to “Identification of substituted benzothiazole sulfones as potent and selective inhibitors of endothelial lipase” [Bioorg. Med. Chem. Lett. 29 (2019) 1918–1921]
38. Ni-electrocatalytic Csp3–Csp3doubly decarboxylative coupling
39. meta C–H Arylation of Electron-Rich Arenes: Reversing the Conventional Site Selectivity
40. Discovery of a Lead Triphenylethanamine Cholesterol Ester Transfer Protein (CETP) Inhibitor
41. Pd II ‐Catalyzed Enantioselective C(sp 3 )−H Activation/Cross‐Coupling Reactions of Free Carboxylic Acids
42. Pd(II)‐Catalyzed Enantioselective C(sp3)–H Activation/Cross‐Coupling Reactions of Free Carboxylic Acids
43. Discovery and synthesis of tetrahydropyrimidinedione-4-carboxamides as endothelial lipase inhibitors
44. Overcoming the Limitations of γ- and δ-C–H Arylation of Amines through Ligand Development
45. A General Amino Acid Synthesis Enabled by Innate Radical Cross-Coupling
46. Versatile Copper-Catalyzed γ-C(sp3)–H Lactonization of Aliphatic Acids
47. Leveraging a “Catch–Release” Logic Gate Process for the Synthesis and Nonchromatographic Purification of Thioether- or Amine-Bridged Macrocyclic Peptides
48. Transient Directing Group Enabled Pd-Catalyzed γ‑C(sp3)–H Oxygenation of Alkyl Amines.
49. Microwave-assisted transamidation of ureas
50. Ligand-Enabled β-C(sp3)–H Olefination of Free Carboxylic Acids
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