689 results on '"Haufe, Günter"'
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2. Influence of N-arylsulfonamido d-valine N-substituents on the selectivity and potency of matrix metalloproteinase inhibitors
3. Towards Optimized Bioavailability of 99mTc-Labeled Barbiturates for Non-invasive Imaging of Matrix Metalloproteinase Activity
4. Reactions of difluoro-pentafluorosulfanyl-iodomethane (SF5CF2I) with electronically different types of alkenes
5. Synthesis and physical chemical properties of CF3O-containg secondary amines—Perspective building blocks for drug discovery
6. Synthesis and application of pentafluorosulfanylation reagents and derived aliphatic SF5-containing building blocks
7. 4-Trifluoromethoxy proline: synthesis of stereoisomers and lipophilicity study.
8. Et3N·3HF Complex Fluorination for Preparing Alkyl Fluorides
9. Synthesis, physico-chemical properties and microsomal stability of compounds bearing aliphatic trifluoromethoxy group
10. Fluorinated Matrix Metalloproteinase Inhibitors (MMPIs) for Potential Application in Therapy and Diagnosis of Diseases
11. Development of symmetric O-BODIPYs with different optical properties as building blocks for the synthesis of ligands for multimodal imaging
12. Straightforward synthesis of fluorinated amino acids by Michael addition of ethyl bromodifluoroacetate to α,β-unsaturated α-amino acid derivatives
13. Diastereoselectivity of cyclopropanation of substituted α-fluorostyrenes versus styrenes by different methods
14. Synthesis and evaluation of a [18F]BODIPY-labeled caspase-inhibitor
15. Preface
16. Selective Synthesis of Monofluorinated Compounds Applying Amine/HF Reagents
17. Synthesis of Diastereomeric 8‐Fluoro‐ABC‐Steroid Building Blocks
18. Halofluorination of N-protected α,β-dehydro-α-amino acid esters—A convenient synthesis of α-fluoro-α-amino acid derivatives
19. Fluorinated matrix metalloproteinases inhibitors—Phosphonate based potential probes for positron emission tomography
20. Et3N·3HF Complex Fluorination for Preparing Alkyl Fluorides
21. Novel fluorine-18 labeled 5-(1-pyrrolidinylsulfonyl)-7-azaisatin derivatives as potential PET tracers for in vivo imaging of activated caspases in apoptosis
22. New matrix metalloproteinase inhibitors based on γ-fluorinated α-aminocarboxylic and α-aminohydroxamic acids
23. Synthesis of new ligands for targeting the S1P1 receptor
24. Pitstop‐2 and its novel derivative RVD ‐127 disrupt global cell dynamics and nuclear pores integrity by direct interaction with small GTPases
25. New approach to α-pentafluorosulfanyl-substituted carboxylic acid derivatives via Ireland-Claisen rearrangements
26. Synthesis of fluorinated analogues of sphingosine-1-phosphate antagonists as potential radiotracers for molecular imaging using positron emission tomography
27. Pitstop‐2 and its novel derivative RVD‐127 disrupt global cell dynamics and nuclear pores integrity by direct interaction with small GTPases.
28. Synthesis, radiosynthesis, in vitro and first in vivo evaluation of a new matrix metalloproteinase inhibitor based on γ-fluorinated α-sulfonylaminohydroxamic acid
29. Influence of 4- or 5-substituents on the pyrrolidine ring of 5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin derivatives on their inhibitory activities towards caspases-3 and -7
30. Synthesis of new fluorinated, 2-substituted 5-pyrrolidinylsulfonyl isatin derivatives as caspase-3 and caspase-7 inhibitors: Nonradioactive counterparts of putative PET-compatible apoptosis imaging agents
31. Putting a Greenhouse Gas to Work
32. Impact of β-perfluoroalkyl substitution of proline on the proteolytic stability of its peptide derivatives
33. Towards Optimized Bioavailability of 99mTc-Labeled Barbiturates for Non-invasive Imaging of Matrix Metalloproteinase Activity
34. Preparation and Characterization of Pentafluoro‐λ 6 ‐sulfanyldifluoromethane and Pentafluoro‐λ 6 ‐sulfanyl‐1,1,2,2‐tetrafluoroethane
35. Fluorinated isatin derivatives. Part 1: Synthesis of new N-substituted ( S)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatins as potent caspase-3 and -7 inhibitors
36. Selective synthesis and self-organization at the air/water interface of long chain fluorinated unsaturated ethyl esters and alcohols
37. MP2 and QCISD(T) study on the convergence of interaction energies of weak O–H⋯F–C, C–H⋯O, and C–H⋯F–C hydrogen bridges
38. Fluorinated phenylcyclopropylamines. Part 5: Effects of electron-withdrawing or -donating aryl substituents on the inhibition of monoamine oxidases A and B by 2-aryl-2-fluoro-cyclopropylamines
39. New synthetic approach to α-fluoro-β-arylvinyl sulfones and their application in Diels–Alder reactions
40. Towards Optimized Bioavailability of 99mTc-Labeled Barbiturates for Non-invasive Imaging of Matrix Metalloproteinase Activity.
41. Synthesis and [3,3]-sigmatropic rearrangements of 5-(pentafluorosulfanyl)-pent-3-en-2-ol, its homologues, and trifluoromethyl analogues
42. New indications for the potential involvement of C–F-bonds in hydrogen bonding
43. Synthesis of ortho-perfluoroalkyl phenones from hemifluorinated enones as key building blocks
44. Preface
45. Synthesis and Biochemical Evaluation of Fluorinated Monoamine Oxidase Inhibitors
46. 18F‐Labeled PET‐Tracers for Cardiological Imaging
47. Synthesis of Fluorine‐Containing 3‐Aminocyclopent‐2‐enones via Intramolecular Cyclization
48. Fluorinated 2-Arylcyclopropan-1-amines – A new class of sigma receptor ligands
49. GABA Analogues and Related Mono-/Bifunctional Building Blocks Derived from the Fluorocyclobutane Scaffold
50. Pentafluorosulfanylation of Aliphatic Substrates
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