179 results on '"Maligres, Peter"'
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2. Selective Synthesis of N6,3′,5′-Tripivaloyladenosine via Dynamic Kinetic Crystallization and Regioselective Preparation of Pivalated 2′-Deoxy-2′-fluoroarabinoadenosines
3. A multifunctional catalyst that stereoselectively assembles prodrugs
4. An approach to heterodiarylmethanes via sp2–sp3 Suzuki−Miyaura cross-coupling
5. Manufacturing Process Development for Uprifosbuvir (MK-3682): A Green and Sustainable Process for Preparing Penultimate 2′-Deoxy-α-2′-Chloro-β-2′-Methyluridine
6. Gasometric titration for dimethylaluminum chloride analysis
7. Diverse Catalytic Reactions for the Stereoselective Synthesis of Cyclic Dinucleotide MK-1454
8. Engineered Ribosyl-1-Kinase Enables Concise Synthesis of Molnupiravir, an Antiviral for COVID-19
9. Discovery and Development of an Unusual Organocatalyst for the Conversion of Thymidine to Furanoid Glycal
10. Organocatalytic Conversion of Nucleosides to Furanoid Glycals
11. Stereocontrolled preparation of a nonpeptidal (-)-spirobicyclic NK-1 receptor antagonist
12. Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods
13. Synthesis of a muscarinic receptor antagonist via a diastereoselective Michael reaction, selective deoxyfluorination and aromatic metal-halogen exchange reaction
14. Evolving to an Ideal Synthesis of Molnupiravir, an Investigational Treatment for COVID-19
15. Preparation of (S)-3-carbethoxy-3-benzylpiperidine and the growth hormone secretagogue L-163,540
16. Discovery and Development of an Unusual Organocatalyst for the Conversion of Thymidine to Furanoid Glycal.
17. Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376
18. Preparation of 2-(2H-Tetrazol-2-yl)benzoic Acids via Regioselective Cu(I) Catalyzed N2 Arylation of Tetrazole
19. A highly catalytic robust palladium catalyzed cyanation of aryl bromides
20. Synthesis of a beta-amino acid pharmacophore via a beta-lactam intermediate
21. ChemInform Abstract: An Approach to Heterodiarylmethanes via sp2—sp3 Suzuki—Miyaura Cross‐Coupling.
22. A Robust Kilo-Scale Synthesis of Doravirine
23. ChemInform Abstract: Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di‐ and Triborylated Indoles.
24. Development of a Kilogram-Scale Asymmetric Synthesis of a Potent DP Receptor Antagonist
25. Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles
26. A Synthesis of a Spirocyclic Macrocyclic Protease Inhibitor for the Treatment of Hepatitis C
27. Enantioselective Synthesis of α-Methyl-β-cyclopropyldihydrocinnamates
28. ChemInform Abstract: Silyl Phosphorus and Nitrogen Donor Chelates for Homogeneous ortho Borylation Catalysis.
29. ChemInform Abstract: Asymmetric Synthesis of Cyclic Indole Aminals via 1,3‐Stereoinduction.
30. Silyl Phosphorus and Nitrogen Donor Chelates for Homogeneous Ortho Borylation Catalysis
31. Asymmetric Synthesis of Cyclic Indole Aminals via 1,3-Stereoinduction
32. ChemInform Abstract: A Traceless Directing Group for C-H Borylation.
33. Enantioselective Synthesis of an HCV NS5a Antagonist
34. A Traceless Directing Group for CH Borylation
35. High-Throughput Optimization of Ir-Catalyzed C–H Borylation: A Tutorial for Practical Applications
36. Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles.
37. ChemInform Abstract: C—O Cross‐Coupling of Activated Aryl and Heteroaryl Halides with Aliphatic Alcohols.
38. ChemInform Abstract: A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper‐Catalyzed C—X Couplings.
39. A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings
40. CO Cross-Coupling of Activated Aryl and Heteroaryl Halides with Aliphatic Alcohols
41. Development of a Second-Generation, Highly Efficient Manufacturing Route for the HIV Integrase Inhibitor Raltegravir Potassium
42. ChemInform Abstract: Preparation of (S)-3-Carbethoxy-3-benzylpiperidine and the Growth Hormone Secretagogue L-163,540.
43. ChemInform Abstract: Thiol Addition to Aryl Propargyl Alcohols under Mild Conditions: An Accelerating Neighboring Group Effect.
44. Development of a Kilogram-Scale Asymmetric Synthesis of a Potent DP Receptor Antagonist
45. Practical, Highly Convergent, Asymmetric Synthesis of a Selective PPARγ Modulator
46. A Synthesis of a Spirocyclic Macrocyclic Protease Inhibitor for the Treatment of Hepatitis C.
47. Highly Regioselective DABCO-Catalyzed Nucleophilic Aromatic Substitution (SNAr) Reaction of Methyl 2,6-Dichloronicotinate with Phenols.
48. Synthesis of a β-Amino Acid Pharmacophore via a β-Lactam Intermediate
49. Enantioselective Hydrogenation of α-Aryloxy α,β-Unsaturated Acids. Asymmetric Synthesis of α-Aryloxycarboxylic Acids.
50. 1‐Hydroxy‐3‐Phenyl‐2‐Propanone
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