132 results on '"Nuhant, Philippe"'
Search Results
2. Modular radical cross-coupling with sulfones enables access to sp³-rich (fluoro)alkylated scaffolds
3. Synthesis of (R)- and (S)-α-trifluoromethyl propanoic acids via asymmetric hydrogenation followed by salt resolution
4. Macrocyclic Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonists
5. Development of a double allylboration reagent targeting 1,5- syn-( E)-diols: application to the synthesis of the C(23)–C(40) fragment of tetrafibricin
6. Practical Kilogram Synthesis of (S)-1-Benzyl-4-Bromo-3-Methyl-1,2,3,6-Tetrahydropyridine
7. Suppression of [T.sub.H]17 differentiation and autoimmunity by a synthetic ROR ligand
8. Discovery and Optimization of a Series of Sulfonamide Inverse Agonists for the Retinoic Acid Receptor-Related Orphan Receptor-α
9. Electrochemically Enabled Chan–Lam Couplings of Aryl Boronic Acids and Anilines
10. Discovery of 3-Cyano-N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist
11. C–H Functionalization of Heteroarenes Using Unactivated Alkyl Halides through Visible-Light Photoredox Catalysis under Basic Conditions
12. Modular radical cross-coupling with sulfones enables access to sp 3 -rich (fluoro)alkylated scaffolds
13. Sulfones: A New Functional Group for Modular Radical Cross-Coupling
14. Enhancement of 5-aminopenta-2,4-dienals electrophilicity via activation by O,N-bistrifluoroacetylation. application to an N-acyl Pictet-Spengler reaction
15. Visible-Light-Initiated Manganese Catalysis for C−H Alkylation of Heteroarenes: Applications and Mechanistic Studies
16. Visible-Light-Driven Photocatalytic Initiation of Radical Thiol–Ene Reactions Using Bismuth Oxide
17. Synthesis of Chiral Azabicycles from Pyroglutaminols
18. ChemInform Abstract: Visible-Light-Driven Photocatalytic Initiation of Radical Thiol-Ene Reactions Using Bismuth Oxide.
19. ChemInform Abstract: Access to Highly Substituted 7-Azaindoles from 2-Fluoropyridines via 7-Azaindoline Intermediates.
20. Visible-Light-Driven Photocatalytic Initiation of Radical Thiol–Ene Reactions Using Bismuth Oxide
21. Identification of a Synthetic Agonist for the Orphan Nuclear Receptors RORα and RORγ, SR1078
22. Access to Highly Substituted 7-Azaindoles from 2-Fluoropyridines via 7-Azaindoline Intermediates
23. Antiproliferation Activity of a Small Molecule Repressor of Liver Receptor Homolog 1
24. ChemInform Abstract: Generation of Stereochemically Defined Tetrasubstituted Enolborinates by 1,4-Hydroboration of α,β-Unsaturated Morpholine Carboxamides with (Diisopinocampheyl)borane.
25. ChemInform Abstract: Diisopinocampheylborane-Mediated Reductive Aldol Reactions: Highly Enantio- and Diastereoselective Synthesis of syn Aldols from N-Acryloylmorpholine.
26. Generation of Stereochemically Defined Tetrasubstituted Enolborinates by 1,4-Hydroboration of α,β-Unsaturated Morpholine Carboxamides with (Diisopinocampheyl)borane
27. (Diisopinocampheyl)borane-Mediated Reductive Aldol Reactions of Acrylate Esters: Enantioselective Synthesis of Anti-Aldols
28. Diisopinocampheylborane‐Mediated Reductive Aldol Reactions: Highly Enantio‐ and Diastereoselective Synthesis of syn Aldols from N‐Acryloylmorpholine
29. Diisopinocampheylborane-Mediated Reductive Aldol Reactions: Highly Enantio- and Diastereoselective Synthesis ofsynAldols fromN-Acryloylmorpholine
30. Enantio- and Diastereoselective Synthesis of N-Acetyl Dihydrotetrafibricin Methyl Ester
31. Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based Strategies
32. Development of a double allylboration reagent targeting 1,5-syn-(E)-diols: application to the synthesis of the C(23)–C(40) fragment of tetrafibricin [Tetrahedron 67 (35) (2011) 6497–6512]
33. ChemInform Abstract: Enantio- and Diastereoselective Synthesis of (E)-1,5-syn-Diols: Application to the Synthesis of the C(23)-C(40) Fragment of Tetrafibricin.
34. Enantio- and Diastereoselective Synthesis of (E)-1,5-syn-Diols: Application to the Synthesis of the C(23)−C(40) Fragment of Tetrafibricin
35. Identification of SR3335 (ML-176): A Synthetic RORα Selective Inverse Agonist
36. Identification of SR1078, a Synthetic Agonist for the Orphan Nuclear Receptors RORα and RORγ
37. Enhancement of 5-Aminopenta-2,4-dienals Electrophilicity via Activation by O,N-Bistrifluoroacetylation. Application to an N-Acyl Pictet−Spengler Reaction
38. Further Insight from Model Experiments into a Possible Scenario Concerning the Origin of Manzamine Alkaloids
39. Synthesis of Polyprenylated Benzoylphloroglucinols by Regioselective Prenylation of Phloroglucinol in an Aqueous Medium
40. Synthetic Studies Towards Bridgehead Diprenyl-Substituted Bicyclo[3.3.1]nonane-2,9-diones as Models for Polyprenylated Acylphloroglucinol Construction
41. α,α‘-Annulation of 2,6-Prenyl-Substituted Cyclohexanone Derivatives with Malonyl Chloride: Application to a Short Synthesis of (±)-Clusianone. Formation and Rearrangement of a Biogenetic-Like Intermediate
42. Antiproliferation Activity of a Small Molecule Repressor of Liver Receptor Homolog 1
43. Suppression of TH17 differentiation and autoimmunity by a synthetic ROR ligand.
44. Identification of SR3335 (ML-176): A Synthetic RORα Selective Inverse Agonist
45. ChemInform Abstract: Diisopinocampheylborane-Mediated Reductive Aldol Reactions: Highly Enantio- and Diastereoselective Synthesis of syn Aldols from N-Acryloylmorpholine.
46. Discovery of 3-Cyano- N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1 H-pyrrolo[2,3- b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist.
47. Visible-Light-Initiated Manganese Catalysis for C-H Alkylation of Heteroarenes: Applications and Mechanistic Studies.
48. Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.
49. Diisopinocampheylborane-mediated reductive aldol reactions: highly enantio- and diastereoselective synthesis of syn aldols from N-acryloylmorpholine.
50. Enantio- and diastereoselective synthesis of (E)-1,5-syn-diols: application to the synthesis of the C(23)-C(40) fragment of tetrafibricin.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.