269 results on '"Soós, Tibor"'
Search Results
2. Reversible covalent c-Jun N-terminal kinase inhibitors targeting a specific cysteine by precision-guided Michael-acceptor warheads
3. Strain‐Release‐Driven Modular Synthesis of Oxetane‐Based Amide Bioisosteres: Concise, Robust and Scalable Approach.
4. Illuminating the multiple Lewis acidity of triaryl-boranes via atropisomeric dative adducts.
5. Bioinspired Synthesis of (–)-Hunterine A: Deciphering a Unique Deconstructive Route
6. Single-Center, but Multipotent Lewis acids: Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts
7. Single-Center, but Multipotent Lewis acids: Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts
8. (−)‐myrtenol and (−)‐α‐pinene: Aggregation pheromone components of the cypress bark beetle Phloeosinus aubei
9. ChemEASTry Europe, the Status of the Chemical Sciences in a Growing Region
10. Strain and Complexity, Passerini and Ugi Reactions of Four‐Membered Heterocycles and Further Elaboration of TOSMIC Product
11. Total Synthesis and Structural Plasticity of Kratom Pseudoindoxyl Metabolites**
12. Correlating electronic and catalytic properties of frustrated Lewis pairs for imine hydrogenation
13. Identification of two aggregation pheromone components from female cypress bark beetles and evaluation of their activity in the laboratory and the field
14. Late‐Stage Formal Double C−H Oxidation of Prenylated Molecules to Alkylidene Oxetanes and Azetidines by Strain‐Enabled Cross‐Metathesis
15. Syntheses and structural plasticity of kratom pseudoindoxyl metabolites
16. Gram-scale syntheses of kratom pseudoindoxyl metabolites: Illuminating the dynamic stereochemistry and the resulting structural plasticity of mitragynine pseudoindoxyl
17. Intertwining Olefin Thianthrenation with Kornblum/Ganem Oxidations: Ene‐type Oxidation to Furnish α,β‐Unsaturated Carbonyls
18. Identification of two female cypress bark beetle pheromone components and evaluation of their activity in the laboratory and the field
19. Syntheses of 2- and 3‑Substituted Morpholine Congeners via Ring Opening of 2‑Tosyl-1,2-Oxazetidine.
20. Structure–Activity Relationships of 8-Hydroxyquinoline-Derived Mannich Bases with Tertiary Amines Targeting Multidrug-Resistant Cancer
21. A 2021-es Kémiai Nobel-díj: organokatalízis, paradigmaváltás a szerves szintézisek és a katalízis területén • The Nobel Prize in Chemistry 2021: Organocatalysis, a Paradigm Shift in Organic Syntheses and Catalysis
22. ChemEASTry Europe, the Status of the Chemical Sciences in a Growing Region.
23. Intertwining Olefin Thianthrenation with Kornblum/Ganem Oxidations: Ene‐type Oxidation to Furnish α,β‐Unsaturated Carbonyls.
24. Genetic Variability of PRRSV Vaccine Strains Used in the National Eradication Programme, Hungary
25. Misleading results of the MboII-based identification of type 2a canine parvovirus strains from Hungary reacting as type 2c strains
26. Total Syntheses of Dihydroindole Aspidosperma Alkaloids: Reductive Interrupted Fischer Indolization Followed by Redox Diversification
27. Total Syntheses of (−)‐Minovincine and (−)‐Aspidofractinine through a Sequence of Cascade Reactions
28. Synthesis of Polyfused Heteroaromatics by Palladium-Catalyzed Cross-Coupling Reaction
29. Fused triazoles and triazolium salts with bridgehead nitrogen atom. Novel syntheses and selective transformations
30. Structural features of the formation of iHOF materials
31. Front Cover: Size-Exclusion Borane-Catalyzed Domino 1,3-Allylic/Reductive Ireland-Claisen Rearrangements: Impact of the Electronic and Structural Parameters on the 1,3-Allylic Shift Aptitude (Chem. Eur. J. 9/2019)
32. Size-Exclusion Borane-Catalyzed Domino 1,3-Allylic/Reductive Ireland-Claisen Rearrangements: Impact of the Electronic and Structural Parameters on the 1,3-Allylic Shift Aptitude
33. Organocatalytic Desymmetrisation of Fittig’s Lactones: Deuterium as a Reporter Tag for Hidden Racemisation
34. Size-Exclusion Borane-Catalyzed Domino 1,3-Allylic/Reductive Ireland-Claisen Rearrangements: Impact of the Electronic and Structural Parameters on the 1,3-Allylic Shift Aptitude
35. A systematic structural study of halogenated 2-phenylbenzimidazoles
36. Sponge-like structures assisted by hydrogen bonds
37. Janus Face of the Steric Effect in a Lewis Acid Catalyst with Size-Exclusion Design: Steric Repulsion and Steric Attraction in the Catalytic Exo-Selective Diels–Alder Reaction
38. Regioexhaustive Functionalization of the Carbocyclic Core of Isoquinoline: Concise Synthesis of Oxoaporphine Core and Ellipticine
39. The Goldilocks Principle in Phase Labeling. Minimalist and Orthogonal Phase Tagging for Chromatography-Free Mitsunobu Reaction
40. Polymorphism of a porous hydrogen bond-assisted ionic organic framework
41. A concise synthesis of furostifoline
42. Is it possible that a Lewis acid has revolving acid strengths?
43. Könyvismertetés: Gálfi P. - Csikós Gy. - Jerzsele Á.: Állatorvosi gyógyszertan III
44. Expanding the Boundaries of Water-Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
45. Auto-Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
46. Front Cover: Schreiner's Thiourea Promoted [2+2] Cycloaddition of Captodative Azetidinones and Nitroolefins (Eur. J. Org. Chem. 11/2017)
47. Schreiner's Thiourea Promoted [2+2] Cycloaddition of Captodative Azetidinones and Nitroolefins
48. Total Syntheses of Dihydroindole AspidospermaAlkaloids: Reductive Interrupted Fischer Indolization Followed by Redox Diversification
49. Expedient and Diastereodivergent Assembly of Terpenoid Decalin Subunits having Quaternary Stereocenters through Organocatalytic Robinson Annulation of Nazarov Reagent
50. Bifunctional Thiourea-Catalyzed Stereoablative Retro-Sulfa-Michael Reaction: Concise and Diastereoselective Access to Chiral 2,4-Diarylthietanes
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.