116 results on '"Auzzas, Luciana"'
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2. Diversity-based synthesis of beta-D-xylo, beta-D-ribo, beta-L-arabino, and beta-L-lyxo 4a-carbafuranoses and (4a-carbafuranosyl)thiols
3. Variable strategy toward carbasugars and relatives. 1. stereocontrolled synthesis of pseudo-beta-D-gulopyranose, pseudo-beta-D-xylofuranose, (pseudo-beta-D-gulopyranosyl)amine, and (pseudo-beta-D-xylofuranosyl)amine
4. The utility of furan-, pyrrole-, and thiophene-based 2-silyloxy dienes as demonstrated by modular synthesis of annonaceous acetogenin core units and their pyrrolidine and thiolane analogues
5. Advances in Chemical Synthesis of Carbasugars and Analogues
6. A short entry to novel C(2)-methyl branched 4a-carbafuranoses
7. Synthesis of N-[4-(propyl)cyclohexyl]-amides with anti-inflammatory and analgesic activities
8. The practice of ring constraint in peptidomimetics using bicyclic and polycyclic amino acids
9. New enantioselective entry to cycloheptane amino acid polyols
10. Enantioselective total synthesis of (1R,3S,4R,5R)-1-amino-4,5-dihydroxycyclopentane-1,3-dicarboxylic acid. A full-aldol access to carbaketose derivatives
11. Variable strategy toward carbasugars and relatives. 6. diastereoselective synthesis of 2-deoxy-2-amino-5a-carba-beta-L-mannopyranuronic acid and 2-deoxy-2amino-5a-carba-beta-L-mannapyranose
12. Focus on preparation of chiral nonracemic medium-sized carbocycles
13. Non-Natural Macrocyclic Inhibitors of Histone Deacetylases: Design, Synthesis, and Activity
14. Nuovi Motivi Azabiciclo [x.2.1] alcanici
15. Sintesi di nuove strutture macrocicliche a ridotta libertà conformazionale
16. Sintesi Totale di Amminoacidi a Base Ciclitolica: un Approccio Orientato alla Diversità
17. Nuove metodologie d'accesso alla diversità molecolare: sintesi di biomolecole e loro insiemi per un utilizzo in agricoltura e terapia
18. Vorinostat-like molecules as structural, stereochemical, and pharmacological tools
19. Non-natural macrocyclic inhibitors of histone deacetylases : design, synthesis, and activity
20. Non-Natural Macrocyclic Inhibitors of Histone Deacetylases: Design, Synthesis, and Activity
21. ChemInform Abstract: Variable Strategy Toward Carbasugars and Relatives as Illustrated by Diastereoselective Synthesis of 1-Deoxy-1-amino-pseudo-β-D-gulopyranose (Alias 1,2,4-Tri-epi-validamine).
22. ChemInform Abstract: Antiinflammatory and Analgesic Amides: New Developments.
23. ChemInform Abstract: Variable Strategy Toward Carbasugars and Relatives. Part 2. Diversity-Based Synthesis of β-D-Xylo, β-D-Ribo, β-L-Arabino, and β-L-Lyxo 4a-Carbafuranoses and (4a-Carbafuranosyl)thiols.
24. Vorinostat-Like Molecules as Structural, Stereochemical, and Pharmacological Tools
25. 4-Aminoproline-based arginine-glycine-aspartate integrin binders with exposed ligation points: practical in-solution synthesis, conjugation and binding affinity evaluation
26. ω-Alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: A study of chain-length and stereochemical dependence
27. ChemInform Abstract: The Practice of Ring Constraint in Peptidomimetics Using Bicyclic and Polycyclic Amino Acids
28. Discovery of Subnanomolar Arginine-Glycine-Aspartate-Based αVβ3/αVβ5 Integrin Binders Embedding 4-Aminoproline Residues
29. Alternative and Expedient Asymmetric Syntheses of l-(+)-Noviose
30. Exploring alternative Zn-binding groups in the design of HDAC inhibitors: Squaric acid, N-hydroxyurea, and oxazoline analogues of SAHA
31. Grafting Aminocyclopentane Carboxylic Acids onto the RGD Tripeptide Sequence Generates Low Nanomolar αVβ3/αVβ5 Integrin Dual Binders
32. Advances in the Chemical Synthesis of Medium-Sized Cyclitols
33. Advances in the Chemical Synthesis of Medium-Sized Cyclitols
34. Advances in Chemical Synthesis of Carbasugars and Analogues
35. Isopavines as a New Class of Morphinomimetics
36. Variable Strategy toward Carbasugars and Relatives. 6.1Diastereoselective Synthesis of 2-Deoxy-2-amino-5a-carba-β-l-mannopyranuronic Acid and 2-Deoxy-2-amino-5a-carba-β-l-mannopyranose
37. Variable Strategy Toward Carbasugars and Relatives. Part 5. Focus on Preparation of Chiral Nonracemic Medium-Sized Carbocycles.
38. Variable Strategy toward Carbasugars and Relatives. 5.1 Focus on Preparation of Chiral Nonracemic Medium-Sized Carbocycles
39. Variable Strategy Toward Carbasugars and Relatives. Part 4. Viable Access to (4a-Carbapentofuranosyl)amines, (5a-Carbahexopyranosyl)amines, and Amino Acids Thereof.
40. Synthesis of a Small Repertoire of Non‐Racemic 5a‐Carbahexopyranoses and 1‐Thio‐5a‐carbahexopyranoses.
41. Variable Strategy toward Carbasugars and Relatives. 4.1 Viable Access to (4a-Carbapentofuranosyl)amines, (5a-Carbahexopyranosyl)amines, and Amino Acids Thereof
42. Variable Strategy toward Carbasugars and Relatives. 2.1 Diversity-Based Synthesis of β-d-Xylo, β-d-Ribo, β-l-Arabino, and β-l-Lyxo 4a-Carbafuranoses and (4a-Carbafuranosyl)thiols
43. ChemInform Abstract: Variable Strategy Toward Carbasugars and Relatives. Part 1. Stereocontrolled Synthesis of Pseudo-β-D-gulopyranose, Pseudo-β-D-xylofuranose, (Pseudo-β-D-gulopyranosyl)amine, and (Pseudo-β-D-xylofuranosyl)amine.
44. Variable Strategy toward Carbasugars and Relatives. 1. Stereocontrolled Synthesis of Pseudo-β-d-gulopyranose, Pseudo-β-d-xylofuranose, (Pseudo-β-d-gulopyranosyl)amine, and (Pseudo-β-d-xylofuranosyl)amine
45. Anti-inflammatory and Analgesic Amides: New Developments
46. Variable Strategy toward Carbasugars and Relatives As Illustrated by Diastereoselective Synthesis of 1-Deoxy-1-amino-pseudo-β-d-gulopyranose (Alias 1,2,4-Tri-epi-validamine)
47. Variable Strategy toward Carbasugars and Relatives. 6. Diastereoselective Synthesis of 2-Deoxy-2-amino-5a-carba-β-L-mannopyranuronic Acid and 2-Deoxy-2-amino-5a-carba-β-L-mannopyranose.
48. Variable Strategy toward Carbasugars and Relatives.4.[sub 1] Viable Access to (4a-Carbapentofuranosyl)amines, (5a-Carbahexopyranosyl)amines, and Amino Acids Thereof.
49. Variable Strategy toward Carbasugars and Relatives.2.[sup 1] Diversity-Based Synthesis ....
50. Synthesis of a Small Repertoire of Non-Racemic 5a-Carbahexopyranoses and 1-Thio-5a-carbahexopyranoses
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