43 results on '"Maligres, Peter E."'
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2. Diverse Catalytic Reactions for the Stereoselective Synthesis of Cyclic Dinucleotide MK-1454
3. Engineered Ribosyl-1-Kinase Enables Concise Synthesis of Molnupiravir, an Antiviral for COVID-19
4. Discovery and Development of an Unusual Organocatalyst for the Conversion of Thymidine to Furanoid Glycal
5. Organocatalytic Conversion of Nucleosides to Furanoid Glycals
6. Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods
7. Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376
8. ChemInform Abstract: An Approach to Heterodiarylmethanes via sp2—sp3 Suzuki—Miyaura Cross‐Coupling.
9. ChemInform Abstract: Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di‐ and Triborylated Indoles.
10. Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles
11. A Synthesis of a Spirocyclic Macrocyclic Protease Inhibitor for the Treatment of Hepatitis C
12. Enantioselective Synthesis of α-Methyl-β-cyclopropyldihydrocinnamates
13. ChemInform Abstract: Silyl Phosphorus and Nitrogen Donor Chelates for Homogeneous ortho Borylation Catalysis.
14. ChemInform Abstract: Asymmetric Synthesis of Cyclic Indole Aminals via 1,3‐Stereoinduction.
15. Silyl Phosphorus and Nitrogen Donor Chelates for Homogeneous Ortho Borylation Catalysis
16. Asymmetric Synthesis of Cyclic Indole Aminals via 1,3-Stereoinduction
17. ChemInform Abstract: A Traceless Directing Group for C-H Borylation.
18. A Traceless Directing Group for CH Borylation
19. A Traceless Directing Group for CH Borylation
20. High-Throughput Optimization of Ir-Catalyzed C–H Borylation: A Tutorial for Practical Applications
21. ChemInform Abstract: C—O Cross‐Coupling of Activated Aryl and Heteroaryl Halides with Aliphatic Alcohols.
22. ChemInform Abstract: A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper‐Catalyzed C—X Couplings.
23. A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings
24. CO Cross-Coupling of Activated Aryl and Heteroaryl Halides with Aliphatic Alcohols
25. CO Cross-Coupling of Activated Aryl and Heteroaryl Halides with Aliphatic Alcohols
26. Development of a Second-Generation, Highly Efficient Manufacturing Route for the HIV Integrase Inhibitor Raltegravir Potassium
27. ChemInform Abstract: Preparation of (S)-3-Carbethoxy-3-benzylpiperidine and the Growth Hormone Secretagogue L-163,540.
28. ChemInform Abstract: Thiol Addition to Aryl Propargyl Alcohols under Mild Conditions: An Accelerating Neighboring Group Effect.
29. Practical, Highly Convergent, Asymmetric Synthesis of a Selective PPARγ Modulator
30. Highly Regioselective DABCO-Catalyzed Nucleophilic Aromatic Substitution (SNAr) Reaction of Methyl 2,6-Dichloronicotinate with Phenols.
31. Highly Regioselective DABCO-Catalyzed Nucleophilic Aromatic Substitution (SNAr) Reaction of Methyl 2,6-Dichloronicotinate with Phenols
32. Enantioselective Hydrogenation of α-Aryloxy α,β-Unsaturated Acids. Asymmetric Synthesis of α-Aryloxycarboxylic Acids.
33. Enantioselective Hydrogenation of α-Aryloxy α,β-Unsaturated Acids. Asymmetric Synthesis of α-Aryloxycarboxylic Acids
34. Preparation of a Clinically Investigated Ras Farnesyl Transferase Inhibitor.
35. Preparation of a clinically investigated ras farnesyl transferase inhibitor
36. ChemInform Abstract: Stereocontrolled Preparation of a Nonpeptidal (‐)‐Spirobicyclic NK‐1 Receptor Antagonist.
37. Stereocontrolled Preparation of a Nonpeptidal (−)-Spirobicyclic NK-1 Receptor Antagonist
38. ChemInform Abstract: A Highly Catalytic Robust Palladium‐Catalyzed Cyanation of Aryl Bromides.
39. Thiol addition to aryl propargyl alcohols under mild conditions: an accelerating neighboring group effect
40. A highly catalytic robust palladium catalyzed cyanation of aryl bromides
41. Preparation of (S)-3-Carbethoxy-3-benzylpiperidine and the Growth Hormone Secretagogue L-163,540
42. Synthesis of the orally active spiroindoline-based growth hormone secretagogue, MK-677
43. Nosylaziridines: Activated aziridine electrophiles
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