41 results on '"Borghi, Daniela"'
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2. Optimization of 6,6-dimethyl pyrrolo[3,4- c]pyrazoles: Identification of PHA-793887, a potent CDK inhibitor suitable for intravenous dosing
3. Stereoselective synthesis of ( Z)-axino- and ( Z)-debromoaxinohydantoin
4. Storage Logistics of Fruits and Vegetables in Distribution Centers
5. Discovery of Stereospecific PARP-1 Inhibitor Isoindolinone NMS-P515
6. D 1 Agonist and/or D 2 antagonist dopamine receptor properties of a series of ergoline derivatives: a structure–activity study
7. Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy
8. Discovery of 2-(Cyclohexylmethylamino)pyrimidines as a New Class of Reversible Valosine Containing Protein Inhibitors
9. LC/MSn and LC/NMR: Two Complentary techniques for the identification of metabolites
10. Total Synthesis of (+)‐7,11‐Helianane and (+)‐5‐Chloro‐7,11‐helianane through Stereoselective Aromatic Claisen Rearrangement
11. Identification of 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors
12. Aplicação de métodos de otimização no cálculo de equilíbrio de misturas de biodiesel com utilização de metodologias rigorosas para estimativa de propriedades termodinâmicas
13. Logistica de armazenamento de frutos e hortaliças em supermercado
14. A Straightforward Total Synthesis of (−)‐Chaetominine
15. A Practical Synthesis of the Major 3-Hydroxy-2-pyrrolidinone Metabolite of a Potent CDK2/Cyclin A Inhibitor.
16. A New Glycociamidine Ring Precursor: Syntheses of (Z)-Hymenialdisine (Ia), (Z)-2-Debromohymenialdisine (Ib), and (.+-.)-endo-2-Debromohymenialdisine (II).
17. Total Synthesis of (.+‐.)‐Cyclooroidin.
18. Total synthesis of (±)-cyclooroidin
19. A New Glycociamidine Ring Precursor: Syntheses of (Z)-Hymenialdisine, (Z)-2-Debromohymenialdisine, and (±)-endo-2-Debromohymenialdisine
20. A practical synthesis of the major 3-hydroxy-2-pyrrolidinone metabolite of a potent CDK2/cyclin A inhibitor
21. Discovery of 2-(Cyclohexylmethylamino)pyrimidinesas a New Class of Reversible Valosine Containing Protein Inhibitors.
22. D1 Agonist and/or D2 antagonist dopamine receptor properties of a series of ergoline derivatives: a structure–activity study
23. Synthesis of 5(10Æ9)abeo-Ergolines
24. Solid state photoreactivity of a dioxolenonemethyl ester
25. Cerium Ammonium Nitrate Promoted Alkoxylation of Cephem Sulfoxides and Sulfones
26. Studies on cephem sulfones as mechanism-based inactivators of human leukocyte elastase. III. Reactions ensuing from chemical β-lactam cleavage
27. Studies on cephem sulfones as mechanism-based inactivators of human leukocyte elastase. IV. Reactions ensuing from enzymatic β-lactam cleavage
28. Metal-catalyzed and -promoted cyclizations for the synthesis of cephalosporins: a possible DAOC/DAC synthetase biomimetic process.
29. Estimation of C13 NMR spectra of organic molecules with the SpecInfo system
30. Synthesis of Penams from 1H-Azetidinones by Intramolecular Carbenoid Insertion
31. Functionalization of the Dihydrothiazine Ring of Cephem Sulfones
32. Stereoselective synthesis of cyclic dinucloetide phosphorothioates
33. D3-Thiazolines, D4-Thiazolines and Thiazoles from Penem Antibiotics
34. Structure Elucidation of Helioscopinolides D and E from Euphorbia calyptrata Cell Cultures
35. Stereoselective alkoxy-de-amination of 7β-Amino-3-Deacetoxy cephalosporanic acid
36. Unexpected Reaction between DCC and Cephalosporanic Acid Sulphones
37. Rearrangement of unsym-azetidinone disulphides to 2β-(thio-substituted methyl) penams
38. Cyclic thiosulfinates and thiosulfonates from oxidation of the 2-thiacephem ring system. Synthesis of (5R)-penems by stereospecific sulfur dioxide extrusion
39. Structure determination of the primary renal metabolite of the penem fce 22101.
40. A straightforward total synthesis of (-)-chaetominine.
41. A new glycociamidine ring precursor: syntheses of (Z)-hymenialdisine, (Z)-2-debromohymenialdisine, and (+/-)-endo-2-debromohymenialdisine.
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