36 results on '"Kaldor, Stephen"'
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2. Discovery of CC-90011: A Potent and Selective Reversible Inhibitor of Lysine Specific Demethylase 1 (LSD1)
3. Design, synthesis and biological evaluation of novel 4-phenylisoquinolinone BET bromodomain inhibitors
4. Discovery of TAK-960: An orally available small molecule inhibitor of polo-like kinase 1 (PLK1)
5. Design and Synthesis of Pyrimidinone and Pyrimidinedione Inhibitors of Dipeptidyl Peptidase IV
6. Discovery of Alogliptin: A Potent, Selective, Bioavailable, and Efficacious Inhibitor of Dipeptidyl Peptidase IV
7. Discovery of Alogliptin: A Potent, Selective, Bioavailable, and Efficacious Inhibitor of Dipeptidyl Peptidase IV
8. Azetidinones as vasopressin V1a antagonists
9. ChemInform Abstract: Expedited Discovery of Second Generation NK‐1 Antagonists: Identification of a Nonbasic Aryloxy Substituent.
10. N-[3-(2-Dimethylaminoethyl)-2-methyl-1H- indol-5-yl]-4-fluorobenzamide: A Potent, Selective, and Orally Active 5-HT1F Receptor Agonist Potentially Useful for Migraine Therapy
11. Expedited discovery of second generation NK-1 antagonists: identification of a nonbasic aryloxy substituent
12. ChemInform Abstract: The Synthesis of Ethanolamine Libraries from Olefin Scaffolds.
13. Solution Phase Synthesis of Libraries of Variably Substituted Olefin Scaffolds: A Library of Allylic Amines
14. The synthesis of ethanolamine libraries from olefin scaffolds
15. Meet the Editorial Board
16. Preface
17. Solid phase synthesis of urea libraries using a diversifiable thiophenoxy carbonyl linker
18. Viracept (Nelfinavir Mesylate, AG1343): A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease
19. 5-HT1F receptor agonists inhibit neurogenic dural inflammation in guinea pigs
20. Synthesis of 2′,3′-dideoxy-3′-hydroxymethylcytidine; a unique antiviral nucleoside
21. Rapid purification of small molecule libraries by ion exchange chromatography
22. Synthesis of 2′,3′-dideoxy-3′-hydroxymethylcytidine: A novel hydroformylation route
23. Discovery of antirhinoviral leads by screening a combinatorial library of ureas prepared using covalent scavengers
24. Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries
25. Solid phase synthesis of hydantoins using a carbamate linker and a novel cyclization / cleavage step
26. Glutamine-derived aldehydes for the inhibition of human rhinovirus 3C protease
27. A Convenient, Large Scale Synthesis of N-CBZ-(S-Phenyl)-L-Cysteine
28. Structure-based drug design of nonpeptidic P2 substituents for HIV-1 protease inhibitors
29. Isophthalic acid derivatives: amino acid surrogates for the inhibition of HIV-1 protease
30. A systematic study of P1–P3 spanning sidechains for the inhibition of HIV-1 protease
31. ITERATIVE PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF HIV PROTEASE INHIBITORS
32. New dipeptide isosteres useful for the inhibition of HIV-1 protease
33. A mild, osmium tetraoxide-catalyzed method for the oxidation of sulfides to sulfones
34. Assignment of stereochemistry in the oligomycin/rutamycin/cytovaricin family of antibiotics. Asymmetric synthesis of the rutamycin spiroketal synthon
35. Total synthesis of the macrolide antibiotic cytovaricin
36. The stereoselective osmylation of 1,1-disubstituted olefins. Effect of allylic substituents on reaction diastereoselectivity
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