Search Results - "Krüll, Jasmin"
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Targeting Drug Resistance in EGFR with Covalent Inhibitors: A Structure-Based Design Approach
Published in Journal of medicinal chemistry (10-09-2015)“…Receptor tyrosine kinases represent one of the prime targets in cancer therapy, as the dysregulation of these elementary transducers of extracellular signals,…”
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[18F]Fluorine‐Labeled Pharmaceuticals: Direct Aromatic Fluorination Compared to Multi‐Step Strategies
Published in Asian journal of organic chemistry (01-05-2019)“…Positron emission tomography (PET) presents an important tool for medicinal and pharmaceutical investigations, with applications ranging from fundamental…”
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3
Inhibitors to Overcome Secondary Mutations in the Stem Cell Factor Receptor KIT
Published in Journal of medicinal chemistry (09-11-2017)“…In modern cancer therapy, the use of small organic molecules against receptor tyrosine kinases (RTKs) has been shown to be a valuable strategy. The association…”
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4
Microwave‐Assisted Rapid One‐Pot Synthesis of Fused and Non‐Fused Indoles and 5‐[18F]Fluoroindoles from Phenylazocarboxylates
Published in Chemistry : a European journal (16-11-2017)“…Substituted indoles can be prepared from phenylazocarboxylates through a rapid one‐pot sequence featuring a microwave‐assisted Fischer indole synthesis as a…”
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5
Sustainable Synthesis of Balsalazide and Sulfasalazine Based on Diazotization with Low Concentrations of Nitrogen Dioxide in Air
Published in Chemistry : a European journal (23-03-2017)“…Low concentrations of nitrogen dioxide, which arises as a side product from a range of industrial processes, can effectively be recycled through the…”
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Inside Cover: Sustainable Synthesis of Balsalazide and Sulfasalazine Based on Diazotization with Low Concentrations of Nitrogen Dioxide in Air (Chem. Eur. J. 17/2017)
Published in Chemistry : a European journal (23-03-2017)“…From waste to valuables: The industrial production of copper nitrate from copper produces large amounts of toxic NO2. Instead of costly denitrification, this…”
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Tuning the Polarity of Antibiotic‐Cy5 Conjugates Enables Highly Selective Labeling of Binding Sites
Published in Chemistry : a European journal (10-08-2023)“…Multidrug‐resistant bacteria pose a major threat to global health, even as newly introduced antibiotics continue to lose their therapeutic value. Against this…”
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Selective Functionalization of Graphene at Defect‐Activated Sites by Arylazocarboxylic tert‐Butyl Esters
Published in Angewandte Chemie International Edition (11-03-2019)“…The development of versatile functionalization concepts for graphene is currently in the focus of research. Upon oxo‐functionalization of graphite, the full…”
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9
Synthesis, Radiosynthesis and Biological Evaluation of Buprenorphine‐Derived Phenylazocarboxamides as Novel μ‐Opioid Receptor Ligands
Published in ChemMedChem (03-07-2020)“…Targeted structural modifications have led to a novel type of buprenorphine‐derived opioid receptor ligand displaying an improved selectivity profile for the…”
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10
Selective functionalization of graphene at defect activated sites by arylazocarboxylic tert-butylesters
Published in Angewandte Chemie International Edition (20-12-2018)“…The development of versatile functionalization concepts for graphene are currently in the focus of research. With oxo-functionalization of graphite the full…”
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Selektive Funktionalisierung von Graphen an defektaktivierten Bereichen durch Arylazocarbonsäure‐tert‐butylester
Published in Angewandte Chemie (11-03-2019)“…Die Entwicklung vielseitiger Funktionalisierungskonzepte für Graphen steht derzeit im Fokus der Forschung. Mittels Oxo‐Funktionalisierung von Graphit wird die…”
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Selektive Funktionalisierung von Graphen an defektaktivierten Bereichen durch Arylazocarbonsäure‐ tert ‐butylester
Published in Angewandte Chemie (11-03-2019)“…Abstract Die Entwicklung vielseitiger Funktionalisierungskonzepte für Graphen steht derzeit im Fokus der Forschung. Mittels Oxo‐Funktionalisierung von Graphit…”
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