34 results on '"Buzard, Daniel"'
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2. C–H activation reactions as useful tools for medicinal chemists
3. Discovery of a novel trans-1,4-dioxycyclohexane GPR119 agonist series
4. Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptor
5. ChemInform Abstract: C—H Activation Reactions as Useful Tools for Medicinal Chemists
6. Discovery and optimization of 5-fluoro-4,6-dialkoxypyrimidine GPR119 agonists
7. Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease
8. An Efficient Scale-Up Process for the Preparation of the APD334 Precursor 4-Chloromethyl-1-cyclopentyl-2-(trifluoromethyl)benzene
9. Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P 1 agonists
10. Agonist/antagonist modulation in a series of 2-aryl benzimidazole H4 receptor ligands
11. (7-Benzyloxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic Acids as S1P1 Functional Antagonists
12. Discovery of APD334: Design of a Clinical Stage Functional Antagonist of the Sphingosine-1-phosphate-1 Receptor
13. Kinetics of 5-HT2BReceptor Signaling: Profound Agonist-Dependent Effects on Signaling Onset and Duration
14. Therapeutic Utility of Cannabinoid Receptor Type 2 (CB2) Selective Agonists
15. Complementary Asymmetric Routes to (R)-2-(7-Hydroxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetate
16. GPR119 agonists 2009–2011
17. Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P1 agonists
18. ChemInform Abstract: Synthesis of a Broad Array of Highly Functionalized, Enantiomerically Pure Cyclohexanecarboxylic Acid Derivatives by Microbial Dihydroxylation of Benzoic Acid and Subsequent Oxidative and Rearrangement Reactions.
19. GPR119 agonists for the treatment of type 2 diabetes
20. Recent progress in the development of selective S1P1 receptor agonists for the treatment of inflammatory and autoimmune disorders
21. Identification of 2-arylbenzimidazoles as potent human histamine H4 receptor ligands
22. Identification of 2-arylbenzimidazoles as potent human histamine H 4 receptor ligands
23. Synthesis of a Broad Array of Highly Functionalized, Enantiomerically Pure Cyclohexanecarboxylic Acid Derivatives by Microbial Dihydroxylation of Benzoic Acid and Subsequent Oxidative and Rearrangement Reactions
24. Alkylations of Functionalized Organozinc Reagents with Allylic EpoxidesCatalyzedby A Cyanocuprate
25. Cuprate-catalyzedThree-Component Couplings of Functionalized Organozinc Reagents
26. TherapeuticUtility of Cannabinoid Receptor Type 2 (CB2) SelectiveAgonists.
27. Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease
28. Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P1 agonists
29. ChemInform Abstract: Diazonaphthoquinones: Synthesis, Reactions and Applications.
30. Alkylations of Functionalized Organozinc Reagents with Allylic Epoxides Catalyzed by A Cyanocuprate.
31. ChemInform Abstract: Synthesis of a Broad Array of Highly Functionalized, Enantiomerically Pure Cyclohexanecarboxylic Acid Derivatives by Microbial Dihydroxylation of Benzoic Acid and Subsequent Oxidative and Rearrangement Reactions.
32. Identification of 2-arylbenzimidazoles as potent human histamine H4 receptor ligands
33. Agonist/antagonist modulation in a series of 2-aryl benzimidazole H4 receptor ligands
34. Kinetics of 5-HT2B receptor signaling: profound agonist-dependent effects on signaling onset and duration.
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