119 results on '"Frackenpohl, Jens"'
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2. Synthesis and biological profile of 2,3-dihydro[1,3]thiazolo[4,5-b]pyridines, a novel class of acyl-ACP thioesterase inhibitors
3. Discovery and optimization of spirocyclic lactams that inhibit acyl‐ACP thioesterase
4. Identifying new lead structures to enhance tolerance towards drought stress via high-throughput screening giving crops a quantum of solace
5. A Study in Scaffold Hopping: Discovery and Optimization of Thiazolopyridines as Potent Herbicides That Inhibit Acyl-ACP Thioesterase.
6. Inspired by Nature: Isostere Concepts in Plant Hormone Chemistry.
7. Designing New Protoporphyrinogen Oxidase-Inhibitors Carrying Potential Side Chain Isosteres to Enhance Crop Safety and Spectrum of Activity.
8. Design, synthesis and screening of herbicidal activity for new phenyl pyrazole‐based protoporphyrinogen oxidase‐inhibitors ( PPO ) overcoming resistance issues
9. Abscisic acid agonists suitable for optimizing plant water use
10. Synthesis and SAR of 2,3‐Dihydro‐1‐benzofuran‐4‐carboxylates: Potent Salicylic Acid‐Based Lead Structures against Plant Stress
11. Synthesis and Exploration of Abscisic Acid Receptor Agonists Against Dought Stress by Adding Constraint to a Tetrahydroquinoline‐Based Lead Structure
12. Recent Advances in the Solid-Phase Synthesis of Long-Chain β-Peptides
13. Synthesis of enantiopure 3-quinuclidinone analogues with three stereogenic centers: (1S,2R,4S)- and (1S,2S,4S)-2-(hydroxymethyl)-1-azabicyclo[2.2.2]octan-5-one and stereocontrol of nucleophilic addition to the carbonyl group
14. Abscisic Acid Receptors and Coreceptors Modulate Plant Water Use Efficiency and Water Productivity
15. Potent Analogues of Abscisic Acid - Identifying Cyano-Cyclopropyl Moieties as Promising Replacements for the Cyclohexenone Headgroup
16. Front Cover: Analogues of Abscisic Acid - Insights into their Activity in Vitro and in Vivo (Eur. J. Org. Chem. 12/2018)
17. Abscisic Acid Receptors and Coreceptors Modulate Plant Water Use Efficiency and Water Productivity.
18. Insights into the in Vitro and in Vivo SAR of Abscisic Acid - Exploring Unprecedented Variations of the Side Chain via Cross-Coupling-Mediated Syntheses.
19. Organic Chemistry ofCinchona Alkaloids
20. Entwicklung von Methoden zur diastereoselektiven Funktionalisierung der Cinchona Alkaloide und Synthese neuartiger funktionalisierter Chinuclidine
21. ChemInform Abstract: Organic Chemistry of Cinchona Alkaloids
22. ChemInform Abstract: Synthesis of 10,11-Didehydro Cinchona Alkaloids and Key Derivatives.
23. Insecticidal heterolignans—Tubuline polymerization inhibitors with activity against chewing pests
24. Synthesis ofβ3-Homophenylalanine-Derived Amino Acids and Peptides bySuzuki Coupling in Solution and on Solid Support
25. Recent Advances in Cinchona Alkaloid Chemistry
26. Recent Advances inCinchonaAlkaloid Chemistry
27. Cover Picture: Recent Advances in Cinchona Alkaloid Chemistry (Eur. J. Org. Chem. 21/2004)
28. Studies on the Asymmetric Dihydroxylation of Advanced Bryostatin C-Ring Segments
29. Syntheses and CD-Spectroscopic Investigations of Longer-Chain -Peptides: Preparation by Solid-Phase Couplings of Single Amino Acids, Dipeptides, and Tripeptides
30. On the Biodegradation of β-Peptides Part of the PhD thesis of J.V.S. Dissertation no. 14298, ETH Zürich, 2001.
31. The outstanding metabolic stability of a14C-labeled?-nonapeptide in rats -in vitro andin vivo pharmacokinetic studies
32. On the Antimicrobial and Hemolytic Activities of Amphiphilic β-Peptides
33. ChemInform Abstract: Cross‐Coupling Reactions in Cinchona Alkaloid Chemistry: Aryl‐Substituted and Dimeric Quinine, Quinidine, as well as Quincorine and Quincoridine Derivatives.
34. The Outstanding Biological Stability ofβ- andγ-Peptides toward Proteolytic Enzymes: An In Vitro Investigation with Fifteen Peptidases
35. The Miraculous CD Spectra (and Secondary Structures?) ofβ-Peptides as They Grow Longer, Preliminary Communication
36. Cross-coupling reactions in Cinchona alkaloid chemistry: aryl-substituted and dimeric quinine, quinidine, as well as quincorine and quincoridine derivatives
37. ChemInform Abstract: Synthesis of Enantiopure 3-Quinuclidinone Analogues with Three Stereogenic Centers: (1S,2R,4S)- and (1S,2S,4S)-2-(Hydroxymethyl)-1-azabicyclo[2.2.2]octan-5-one and Stereocontrol of Nucleophilic Addition to the Carbonyl Group.
38. ChemInform Abstract: Synthesis of Enantiopure 1‐Azabicyclo[3.2.2]nonanes via Stereoselective Capture of Chiral Carbocations.
39. Synthesis of Enantiopure 3-Quinuclidinone Analogues with Three Stereogenic Centers: (1S,2R,4S)-and(1S,2S,4S)-2-(Hydroxymethyl)-1-azabicyclo[2.2.2]octan-5-one and Stereocontrol of Nucleophilic Addition to the Carbonyl Group
40. Synthesis of Enantiopure 1-Azabicyclo[3.2.2]nonanes via Stereoselective Capture of Chiral Carbocations
41. Synthesis of 10,11-DidehydroCinchona Alkaloids and Key Derivatives
42. Morphin und Opioid-Analgetika
43. Novel Bridged Bicyclic α-Amino Acid Esters and Key Derivatives from Quincorine and Quincoridine
44. Synthesis of oxazatwistanes and their homo- and bishomo-analogues from quinidine — Medium ring systems derived from cinchona alkaloids
45. 1,2-Carbonyl Transposition of a Protected Rubanone: Stereoselective synthesis of bicyclic and tricyclic lactams derived from quinidine
46. Synthesis of tricyclic N,O-acetals from α-functionalized rubanone. A masked 1,2,3-tricarbonyl system from quinidine
47. Cleavage of sulfonamides with phenyldimethylsilyllithium
48. Front Cover: Synthesis and SAR of 2,3‐Dihydro‐1‐benzofuran‐4‐carboxylates: Potent Salicylic Acid‐Based Lead Structures against Plant Stress (Eur. J. Org. Chem. 14/2022).
49. The outstanding metabolic stability of a 14C-labeled β-nonapeptide in rats - in vitro and in vivo pharmacokinetic studies.
50. The Outstanding Biological Stability of β- and γ-Peptides toward Proteolytic Enzymes: An In Vitro Investigation with Fifteen Peptidases.
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