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3. Using nature’s blueprint to expand catalysis with Earth-abundant metals

6. Streamlined Three-Step Telescope Enabled by a Nonaqueous Suzuki–Miyaura Cross-Coupling Reaction

7. Impact of ICH Q11 Questions and Answers on the Outcome of Active Pharmaceutical Ingredient Starting Material Proposal Acceptance by ICH Regulatory Members

9. Quinone-mediated hydrogen anode for non-aqueous reductive electrosynthesis

12. Coupling-Condensation Strategy for the Convergent Synthesis of an Imidazole-Fused 2-Aminoquinoline NLRP3 Agonist

16. High Bulk-Density Amorphous Dispersions to Enable Direct Compression of Reduced Tablet Size Amorphous Dosage Units

17. Kilo-Scale Electrochemical Oxidation of a Thioether to a Sulfone: A Workflow for Scaling up Electrosynthesis

19. Leveraging High-Throughput Experimentation to Drive Pharmaceutical Route Invention: A Four-Step Commercial Synthesis of Branebrutinib (BMS-986195)

20. Cesium Amide‐Catalyzed Selective Deuteration of Benzylic C‐H Bonds with D2 and Application for Tritiation of Pharmaceuticals.

25. Engineered Ribosyl-1-Kinase Enables Concise Synthesis of Molnupiravir, an Antiviral for COVID-19

30. Mechanism of cyclopropanol to cyclopropanol isomerization mediated by Ti(IV) and a Lewis acid (1)

34. Evolving to an Ideal Synthesis of Molnupiravir, an Investigational Treatment for COVID-19

38. Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376

41. Using nature’s blueprint to expand catalysis with Earth-abundant metals

47. A biochemical GC-MS application for the organic chemistry laboratory: determination of fatty acid composition of Arabidposis thaliana lipids

48. Concise Synthesis of Furo[2,3- b ]indolines via [3,3]-Sigmatropic Rearrangement of N -Alkenyloxyindoles.

49. Late‐Stage 18O Labeling of Primary Sulfonamides via a Degradation–Reconstruction Pathway.

50. C–H Arylation in the Formation of a Complex Pyrrolopyridine, the Commercial Synthesis of the Potent JAK2 Inhibitor, BMS-911543

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