49 results on '"Bo, Yunxin"'
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2. Synthesis and X-ray crystal structure of (−)-calicheamicinone
3. New, practical and effective sources of fluoride ion for desilylation to form carbon anions
4. The imidazo[1,2-a]pyridine ring system as a scaffold for potent dual phosphoinositide-3-kinase (PI3K)/mammalian target of rapamycin (mTOR) inhibitors
5. Synthesis and structure–activity relationships of dual PI3K/mTOR inhibitors based on a 4-amino-6-methyl-1,3,5-triazine sulfonamide scaffold
6. Small Molecule Disruptors of the Glucokinase–Glucokinase Regulatory Protein Interaction: 5. A Novel Aryl Sulfone Series, Optimization Through Conformational Analysis
7. Enantioselective total synthesis of asidophytine
8. Highly enantioselective phase transfer catalyzed alkylation of a 3-oxygenated propionic ester equivalent: applications and mechanism
9. Synthesis of (+ or -)-calicheamicinone by two related methods
10. Optimization of Potency and Pharmacokinetic Properties of Tetrahydroisoquinoline Transient Receptor Potential Melastatin 8 (TRPM8) Antagonists
11. Substituted aryl pyrimidines as potent and soluble TRPV1 antagonists
12. Correction to Selective Class I Phosphoinositide 3-Kinase Inhibitors: Optimization of a Series of Pyridyltriazines Leading to the Identification of a Clinical Candidate, AMG 511
13. Selective Class I Phosphoinositide 3-Kinase Inhibitors: Optimization of a Series of Pyridyltriazines Leading to the Identification of a Clinical Candidate, AMG 511
14. Structure-Based Design of a Novel Series of Potent, Selective Inhibitors of the Class I Phosphatidylinositol 3-Kinases
15. Fused Piperidines as a Novel Class of Potent and Orally Available Transient Receptor Potential Melastatin Type 8 (TRPM8) Antagonists
16. Phospshoinositide 3-Kinase (PI3K)/Mammalian Target of Rapamycin (mTOR) Dual Inhibitors: Discovery and Structure–Activity Relationships of a Series of Quinoline and Quinoxaline Derivatives
17. ChemInform Abstract: Synthesis and X-Ray Crystal Structure of (-)-Calicheamicinone.
18. ChemInform Abstract: New, Practical and Effective Sources of Fluoride Ion for Desilylation to Form Carbon Anions.
19. ChemInform Abstract: Enantioselective Total Synthesis of Aspidophytine (I).
20. Novel Vanilloid Receptor-1 Antagonists: 2. Structure−Activity Relationships of 4-Oxopyrimidines Leading to the Selection of a Clinical Candidate
21. Novel Vanilloid Receptor-1 Antagonists: 1. Conformationally Restricted Analogues of trans-Cinnamides
22. Design of Potent, Orally Available Antagonists of the Transient Receptor Potential Vanilloid 1. Structure−Activity Relationships of 2-Piperazin-1-yl-1H-benzimidazoles
23. Synthesis and evaluation of thiazole carboxamides as vanilloid receptor 1 (TRPV1) antagonists
24. Melanocortin subtype-4 receptor agonists containing a piperazine core with substituted aryl sulfonamides
25. Discovery of Potent, Orally Available Vanilloid Receptor-1 Antagonists. Structure−Activity Relationship of N-Aryl Cinnamides
26. ChemInform Abstract: Synthetic Studies on Calicheamicin γI1 — Synthesis of (‐)‐Calicheamicinone and Models Representing the Four Sugars and the Aromatic System
27. Synthetic studies on calicheamicin γ1I—synthesis of(−)-calicheamicinone and models representing the four sugars and the aromatic system
28. Optimization of Potency andPharmacokinetic Propertiesof Tetrahydroisoquinoline Transient Receptor Potential Melastatin8 (TRPM8) Antagonists.
29. ChemInform Abstract: Highly Enantioselective Phase Transfer Catalyzed Alkylation of a 3‐Oxygenated Propionic Ester Equivalent: Applications and Mechanism.
30. Synthesis and X-ray crystal structure of (?)-calicheamicinone
31. Synthesis of (±)-Calicheamicinone by Two Methods
32. Synthesis of (±)-Calicheamicinone by Two Related Methods
33. Selective Class I Phosphoinositide3-KinaseInhibitors: Optimization of a Series of Pyridyltriazines Leading tothe Identification of a Clinical Candidate, AMG 511.
34. Structure-Based Designof a Novel Series of Potent, Selective Inhibitors of the Class IPhosphatidylinositol 3-Kinases.
35. Fused Piperidines as aNovel Class of Potent and OrallyAvailable Transient Receptor Potential Melastatin Type 8 (TRPM8) Antagonists.
36. Phospshoinositide 3-Kinase (PI3K)/Mammalian Target of Rapamycin (mTOR) Dual Inhibitors: Discovery and StructureâActivity Relationships of a Series of Quinoline and Quinoxaline Derivatives.
37. Synthese von Heterocyclen durch Tandem‐reaktionen: Beckmann‐Umlagerungen/Allylsilan‐Cyclisierungen
38. Synthesis of Heterocycles by Tandem Reactions: Beckmann Rearrangements/Allylsilane Cyclizations
39. A facile and efficient method for macrolactamization
40. Synthesis of (...)-Calicheamicinone by Two Methods.
41. Design of Potent, Orally Available Antagonists of the Transient Receptor Potential Vanilloid 1. Structure−Activity Relationships of 2-Piperazin-1-yl-1H-benzimidazoles
42. Synthetic studies on calicheamicin γ<SUB>1</SUB><SUP>I</SUP>synthesis of(−)-calicheamicinone and models representing the four sugars and the aromatic system
43. ChemInform Abstract: Synthetic Studies on Calicheamicin γI1 - Synthesis of (-)-Calicheamicinone and Models Representing the Four Sugars and the Aromatic System.
44. ChemInform Abstract: Enantioselective Total Synthesis of Aspidophytine (I).
45. ChemInform Abstract: Synthesis and X-Ray Crystal Structure of (-)-Calicheamicinone.
46. ChemInform Abstract: New, Practical and Effective Sources of Fluoride Ion for Desilylation to Form Carbon Anions.
47. Novel vanilloid receptor-1 antagonists: 2. Structure-activity relationships of 4-oxopyrimidines leading to the selection of a clinical candidate.
48. Design of potent, orally available antagonists of the transient receptor potential vanilloid 1. Structure-activity relationships of 2-piperazin-1-yl-1H-benzimidazoles.
49. Discovery of potent, orally available vanilloid receptor-1 antagonists. Structure-activity relationship of N-aryl cinnamides.
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