388 results on '"Yee, Nathan K."'
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2. The chemistry of Ru cyclopropylmethylidene complexes: Mechanistic studies and synthetic implications for the ring-closing metathesis reaction
3. Copper-catalyzed asymmetric hydrogenation of 2-substituted ketones via dynamic kinetic resolution† †Electronic supplementary information (ESI) available. CCDC 1816601 and 1816602. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8sc00434j
4. Activation of TMSCN by N-heterocyclic carbenes for facile cyanosilylation of carbonyl compounds
5. Olefin ring-closing metathesis as a powerful tool in drug discovery and development – potent macrocyclic inhibitors of the hepatitis C virus NS3 protease
6. A practical and improved synthesis of (3S,5S)-3-[(tert-butyloxycarbonyl)methyl]-5-[(methanesulfonyloxy)methyl]-2-pyrrolidinone
7. A concise synthesis of fusaric acid and (S)-(+)-fusarinolic acid
8. Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More—Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420
9. Nickel-Catalyzed Cross-Electrophile Reductive Couplings of Neopentyl Bromides with Aryl Bromides
10. Synthesis of stable isotope-labelled firocoxib
11. Rational Design of New Dihydrobenzooxophosphole-Based Lewis Base Organocatalysts
12. Synthesis of Cell Adhesion Inhibitors via Crystallization-Driven Dynamic Transformations
13. Practical synthesis of a enantiomerically pure trans-4,5-disubstituted 2-pyrrolidinone via enzymatic resolution. Preparation of the LTB4 inhibitor BIRZ-227
14. Practical synthesis of a cell adhesion inhibitor by self-regeneration of stereocenters
15. Application of a Preformed Pd-BIDIME Precatalyst to Suzuki–Miyaura Cross-Coupling Reaction in Flow
16. Early Development Scale-Up of a Structurally-Challenging 5-Lipoxygenase Activating Protein (FLAP) Inhibitor
17. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights
18. Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4‑Quinolinyl Ethers and MoreApplication to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420.
19. Abstract 960: Defined cell composition and precise control over JCAR017 dose enables identification of relationships between chimeric antigen receptor T cell product attributes, pharmacokinetics, and clinical endpoints in NHL
20. BABIPhos Family of Biaryl Dihydrobenzooxaphosphole Ligands for Asymmetric Hydrogenation
21. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights
22. Development of a Scalable, Chromatography-Free Synthesis of t-Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3-Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation
23. Copper catalyzed asymmetric propargylation of aldehydes
24. Copper-catalyzed annulation of 2-formylazoles with o-aminoiodoarenes
25. A facile and practical synthesis of N-acetyl enamides
26. Epimerization reaction of a substituted vinylcyclopropane catalyzed by ruthenium carbenes: Mechanistic analysis
27. Efficient large-scale synthesis of BILN 2061, a potent HCV protease inhibitor, by a convergent approach based on ring-closing metathesis
28. Early Development Scale-Up of a Structurally-Challenging 5-Lipoxygenase Activating Protein (FLAP) Inhibitor
29. Enantioselective Nickel-Catalyzed Mizoroki–Heck Cyclizations To Generate Quaternary Stereocenters
30. Synthesis of P-Chiral Dihydrobenzooxaphosphole Core for BI Ligands in Asymmetric Transformations
31. Effective BI-DIME Ligand for Suzuki-Miyaura Cross-Coupling Reactions in Water with 500 ppm Palladium Loading and Triton X
32. Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement
33. Sequential C–H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor
34. Enantioselective Arylation of Oxindoles Using Modified BI-DIME Ligands.
35. Modular Dihydrobenzoazaphosphole Ligands for Suzuki-Miyaura Cross-Coupling.
36. Reengineered BI‐DIME Ligand Core Based on Computer Modeling to Increase Selectivity in Asymmetric Suzuki–Miyaura Coupling for the Challenging Axially Chiral HIV Integrase Inhibitor
37. Synthesis of Enantioenriched 2-Alkyl Piperidine Derivatives through Asymmetric Reduction of Pyridinium Salts
38. Construction of Quaternary Stereocenters by Nickel‐Catalyzed Heck Cyclization Reactions
39. ChemInform Abstract: Efficient Iron-Catalyzed Kumada Cross-Coupling Reactions Utilizing Flow Technology under Low Catalyst Loadings.
40. Rhodium-Catalyzed Asymmetric Allenylation of Sulfonylimines and Application to the Stereospecific Allylic Allenylation
41. Development of a Practical Process for the Synthesis of PDE4 Inhibitors
42. ChemInform Abstract: Synthesis of P-Chiral Dihydrobenzooxaphospholes Through Negishi Cross-Coupling.
43. Efficient Iron-Catalyzed Kumada Cross-Coupling Reactions Utilizing Flow Technology under Low Catalyst Loadings
44. Ligand-Accelerated Stereoretentive Suzuki–Miyaura Coupling of Unprotected 3,3′-Dibromo-BINOL
45. Nickel-catalyzed C-3 direct arylation of pyridinium ions for the synthesis of 1-azafluorenes
46. Synthesis of P-Chiral Dihydrobenzooxaphospholes Through Negishi Cross-Coupling
47. Development of an Efficient Synthesis of (2-Aminopyrimidin-5-yl) Boronic Acid
48. BABIPhos Family of Biaryl Dihydrobenzooxaphosphole Ligands for Asymmetric Hydrogenation.
49. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights.
50. Development of a Practical Sequence for Difluoromethylation of 2-Bromopyridines via Copper-Mediated Reductive Coupling and Decarboxylation
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