133 results on '"Gerona‐Navarro, Guillermo"'
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2. Control of Embryonic Stem Cell Identity by BRD4-Dependent Transcriptional Elongation of Super-Enhancer-Associated Pluripotency Genes
3. Selective Chemical Modulation of Gene Transcription Favors Oligodendrocyte Lineage Progression
4. A Small Molecule Binding to the Coactivator CREB-Binding Protein Blocks Apoptosis in Cardiomyocytes
5. Structural Basis of Site-Specific Histone Recognition by the Bromodomains of Human Coactivators PCAF and CBP/p300
6. Exploring solid-phase approaches for the preparation of new β-lactams from amino acids
7. General approach for the stereocontrolled construction of the beta-lactam ring in amino acid-derived 4-alkyl-4-carboxy-2-azetidinones
8. Entry to new conformationally constrained amino acids. First synthesis of 3-unsubstituted 4-alkyl-4-carboxy-2-azetidinone derivatives via an intramolecular N (super)alpha -C (super)alpha -cyclization strategy
9. Abstract PO-008: Bithioether Stapled Peptides as Allosteric Inhibitors of PRC2 function
10. Ligand Discovery Using Small Molecule Microarrays
11. Advances in the Development of Non-steroidal Mineralocorticoidreceptor Antagonists
12. Advances in the Development of Non-steroidal Mineralocorticoid-receptor Antagonists
13. Memory of chirality in the stereoselective synthesis of β-lactams: importance of the starting amino acid derivative
14. In silico design and molecular basis for the selectivity of Olinone toward the first over the second bromodomain of BRD4
15. Peptidomimetics Targeting Protein-Protein Interactions for Therapeutic Development
16. In silico design and molecular basis for the selectivity of Olinone toward the first over the second bromodomain of BRD4.
17. A Solid‐Phase Approach to Accessing Bisthioether‐Stapled Peptides Resulting in a Potent Inhibitor of PRC2 Catalytic Activity
18. Further evidence for 2-alkyl-2-carboxyazetidines as [gamma]-turn inducers
19. Modulating Mineralocorticoid Receptor with Non-steroidal Antagonists. New Opportunities for the Development of Potent and Selective Ligands without Off-Target Side Effects
20. Modulating Mineralocorticoid Receptor with Non-steroidal Antagonists. New Opportunities for the Development of Potent and Selective Ligands without Off-Target Side Effects
21. Cyclic amino acid linkers stabilizing key loops of brain derived neurotrophic factor
22. Assembling Ligands In Situ Using Bioorthogonal Boronate Ester Synthesis
23. Peptidomimetics Targeting Protein-Protein Interactions for Therapeutic Development
24. Solid-Phase Synthesis of a Library of Amphipatic Hydantoins. Discovery of New Hits for TRPV1 Blockade
25. ChemInform Abstract: Entry to New Conformationally Constrained Amino Acids. First Synthesis of 3-Unsubstituted 4-Alkyl-4-carboxy-2-azetidinone Derivatives via an Intramolecular Nα-Cα-Cyclization Strategy.
26. ChemInform Abstract: General Approach for the Stereocontrolled Construction of the β-Lactam Ring in Amino Acid-Derived 4-Alkyl-4-carboxy-2-azetidinones.
27. Further Evidence for 2-Alkyl-2-carboxyazetidines as γ-Turn Inducers
28. 2-Alkyl-2-carboxy-azetidines as scaffolds for the induction of γ-turns
29. Azetidine-Derived Amino Acids versus Proline Derivatives. Alternative Trends in Reverse Turn Induction
30. From 1-Acyl-β-lactam Human Cytomegalovirus Protease Inhibitors to 1-Benzyloxycarbonylazetidines with Improved Antiviral Activity. A Straightforward Approach To Convert Covalent to Noncovalent Inhibitors
31. Ligand Discovery Using Small Molecule Microarrays
32. Synthesis and anti‐HCMV Activity of 1‐Acyl‐β‐lactams and 1‐Acylazetidines Derived from Phenylalanine.
33. Exploring Different Approaches for the Stereoselective Synthesis of Amino Acid Derived 4‐Alkyl‐4‐carboxy‐2‐azetidinones
34. Synthesis and anti-HCMV activity of 1-acyl-β-lactams and 1-acylazetidines derived from phenylalanine
35. Simple access to novel azetidine-containing conformationally restricted amino acids by chemoselective reduction of β-lactams
36. Easy Access to Orthogonally Protected α‐Alkyl Aspartic Acid and α‐Alkyl Asparagine Derivatives by Controlled Opening of β‐Lactams.
37. Memory of Chirality in the Stereoselective Synthesis of β‐Lactams: Importance of the Starting Amino Acid Derivative.
38. Memory of Chirality in the Enantioselective Synthesis of β-Lactams Derived from Amino Acids. Influence of the Reaction Conditions.
39. Easy access to orthogonally protected α-alkyl aspartic acid and α-alkyl asparagine derivatives by controlled opening of β-lactams
40. Memory of Chirality in theEnantioselective Synthesis of β-Lactams Derived from AminoAcids. Influence of the Reaction Conditions
41. ChemInform Abstract: Amino Acid Derived 4‐Alkyl‐4‐carboxy‐2‐azetidinones. New Insights into β‐Lactam Ring Formation and N‐Deprotection.
42. General Approach for the Stereocontrolled Construction of the β-Lactam Ring in Amino Acid-Derived 4-Alkyl-4-carboxy-2-azetidinones
43. Amino Acid-derived 4-Alkyl-4-carboxy-2-azetidinones. New Insights into b-Lactam Ring Formation and N-Deprotection
44. Entry to New Conformationally Constrained Amino Acids. First Synthesis of 3-Unsubstituted 4-Alkyl-4-carboxy-2-azetidinone Derivatives via an Intramolecular Nα-Cα-Cyclization Strategy
45. ChemInform Abstract: New Conformationally Constrained Tryptophans by Nα‐Cα‐Cyclization to an Azetidin‐2‐one Core.
46. Exploring solid-phase approaches for the preparation of new -lactams from amino acids
47. Rational Design of Cyclic Peptide Modulators of the Transcriptional Coactivator CBP: A New Class of p53 Inhibitors.
48. New Conformationally Constrained Tryptophans by Nα-Cα-Cyclization to an Azetidin-2-one Core.
49. Exploring solid-phase approaches for the preparation of new beta-lactams from amino acids
50. Memory of Chirality in the Enantioselective Synthesis of β-Lactams Derived from Amino Acids. Influence of the Reaction Conditions.
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