38 results on '"Corte, James R."'
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2. Methyl-2,2-difluoro-2-(fluorosulfonyl) acetate (MDFA)/copper (I) iodide mediated and tetrabutylammonium iodide promoted trifluoromethylation of 1-aryl-4-iodo-1,2,3-triazoles
3. Emerging Targets for the Treatment of Non-Alcoholic Steatohepatitis (NASH)
4. Orally bioavailable pyridine and pyrimidine-based Factor XIa inhibitors: Discovery of the methyl N-phenyl carbamate P2 prime group
5. Discovery of Milvexian, a High-Affinity, Orally Bioavailable Inhibitor of Factor XIa in Clinical Studies for Antithrombotic Therapy
6. Orally bioavailable amine-linked macrocyclic inhibitors of factor XIa
7. Structure based design of macrocyclic factor XIa inhibitors: Discovery of cyclic P1 linker moieties with improved oral bioavailability
8. Discovery of Milvexian, a High-Affinity, Orally Bioavailable Inhibitor of Factor XIa in Clinical Studies for Antithrombotic Therapy.
9. Discovery of a High Affinity, Orally Bioavailable Macrocyclic FXIa Inhibitor with Antithrombotic Activity in Preclinical Species
10. Potent, Orally Bioavailable, and Efficacious Macrocyclic Inhibitors of Factor XIa. Discovery of Pyridine-Based Macrocycles Possessing Phenylazole Carboxamide P1 Groups
11. Characterization of a new class of selective nonsteroidal progesterone receptor agonists
12. Macrocyclic factor XIa inhibitors
13. Macrocyclic inhibitors of Factor XIa: Discovery of alkyl-substituted macrocyclic amide linkers with improved potency
14. Novel phenylalanine derived diamides as Factor XIa inhibitors
15. Structure-based design of inhibitors of coagulation factor XIa with novel P1 moieties
16. Pyridine and pyridinone-based factor XIa inhibitors
17. Structure-Based Design of Macrocyclic Factor XIa Inhibitors: Discovery of the Macrocyclic Amide Linker
18. Potent, Orally Bioavailable, and Efficacious Macrocyclic Inhibitors of Factor XIa. Discovery of Pyridine-Based Macrocycles Possessing Phenylazole Carboxamide P1 Groups
19. Phenylimidazoles as Potent and Selective Inhibitors of Coagulation Factor XIa with in Vivo Antithrombotic Activity
20. Structure–activity relationships of anthranilamide-based factor Xa inhibitors containing piperidinone and pyridinone P4 moieties
21. ChemInform Abstract: Total Synthesis of (+)-Saponaceolide B
22. Phenylimidazoles as Potentand Selective Inhibitorsof Coagulation Factor XIa with in Vivo Antithrombotic Activity.
23. Discovery of novel 1-arylmethyl pyrrolidin-2-yl ethanol amines as calcium-sensing receptor antagonists
24. Efficient Synthesis of 2-Aryl-6-chloronicotinamides via PXPd2-Catalyzed Regioselective Suzuki Coupling.
25. ChemInform Abstract: Towards the Total Synthesis of Saponaceolides: Synthesis of cis‐2,4‐Disubstituted 3,3‐Dimethylmethylenecyclohexanes.
26. Towards the Total Synthesis of Saponaceolides: Synthesis ofcis-2,4-Disubstituted 3,3-Dimethylmethylenecyclohexanes
27. Total Synthesis of (+)-Saponaceolide B
28. Totalsynthese von (+)-Saponaceolid B
29. Untersuchungen zur Totalsynthese der Saponaceolide: Synthese voncis-2,4-disubstituierten 3,3-Dimethylmethylencyclohexanen
30. The dicobalt hexacarbonyl(alkyne) moiety as a stereocontrol element in intramolecular Friedel–Crafts alkylations1
31. Use of dicobalt hexacarbonyl-estabilized propargyl cations in intramolecular Friedel-Crafts alkylations
32. Towards the Total Synthesis of Saponaceolides: Synthesis of cis-2,4-Disubstituted 3,3-Dimethylmethylenecyclohexanes.
33. Triazole N-linked Carbamoyl Cyclohexyl Acids As Lpa Antagonists
34. Carbamoyloxymethyl Triazole Cyclohexyl Acids As Lpa Antagonists
35. Untersuchungen zur Totalsynthese der Saponaceolide: Synthese von cis-2,4-disubstituierten 3,3-Dimethylmethylencyclohexanen
36. ChemInform Abstract: Total Synthesis of (+)-Saponaceolide B.
37. Synthesis and characterization of 3-arylquinazolinone and 3-arylquinazolinethione derivatives as selective estrogen receptor beta modulators.
38. Efficient synthesis of 2-aryl-6-chloronicotinamides via PXPd2-catalyzed regioselective Suzuki coupling.
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