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2. Preface

4. Discovery of hydroxy pyrimidine Factor IXa inhibitors

6. Direct plasma analysis of drug compounds using monolithic column liquid chromatography and tandem mass spectrometry

8. Synthesis of mono- and difluoronaphthoic acids

9. Stereochemistry of the oxidation of imines derived from substtituted cyclohexanones: axial vs equatorial attack and evidence for delivery by an adjacent hydroxyl group

10. Total synthesis of (+)-himbacine and (+)-himbeline

11. Discovery of MK-8282 as a Potent G-Protein-Coupled Receptor 119 Agonist for the Treatment of Type 2 Diabetes

12. Asymmetric synthesis of substituted 2-azaspiro(3.5)nonan-1-ones: an enantioselective synthesis of the cholesterol absorption inhibitor (+)-SCH 54016

14. Total synthesis of (-)-himgaline

15. Design and Synthesis of P2–P4 Macrocycles Containing a Unique Spirocyclic Proline: A New Class of HCV NS3/4A Inhibitors

18. Discovery of MK-8831, A Novel Spiro-Proline Macrocycle as a Pan-Genotypic HCV-NS3/4a Protease Inhibitor

21. Diaryl piperidines as CB 1 receptor antagonists

23. A highly efficient total synthesis of (+)-himbacine

25. Novel Quinoline-Based P2–P4 Macrocyclic Derivatives As Pan-Genotypic HCV NS3/4a Protease Inhibitors

29. Discovery of a vorapaxar analog with increased aqueous solubility

36. Diaryl piperidines as CB1 receptor antagonists

40. Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonists

41. Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonists

42. Discovery of a Novel, Orally Active Himbacine-Based Thrombin Receptor Antagonist (SCH 530348) with Potent Antiplatelet Activity

44. Heterotricyclic Himbacine Analogs as Potent, Orally Active Thrombin Receptor (Protease Activated Receptor-1) Antagonists

45. Total Synthesis of (‐)‐Himgaline (I).

46. Metabolism-Based Identification of a Potent Thrombin Receptor Antagonist

48. Total Synthesis of (−)-Himgaline

49. Himbacine derived thrombin receptor (PAR-1) antagonists: Structure–activity relationship of the lactone ring

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