UB Paderborn / Katalog / Suche / in CDI

Fluoro-Pummerer rearrangement and analogous reactions

Journal of fluorine chemistry, 2012-11, Vol.143, p.238-262

2012

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The Gordian Knot 2.0 - Decentralized production of radiopharmaceuticals

Nuklearmedizin. Nuclear medicine, 2019-12, Vol.58 (6), p.420

2019

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GMP-Compliant Radiosynthesis of [18F]GP1, a Novel PET Tracer for the Detection of Thrombi

Pharmaceuticals (Basel, Switzerland), 2021-07, Vol.14 (8), p.739

2021

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Optimized Treatment and Recovery of Irradiated [18O]-Water in the Production of [18F]-Fluoride

Instruments (Basel), 2018-09, Vol.2 (3), p.12

2018

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Oxidative desulfurization-fluorination of thioethers. Application for the synthesis of fluorinated nitrogen containing building blocks

Organic & biomolecular chemistry, 2010-12, Vol.8 (24), p.5682-5691

2010

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Synthesis, radiosynthesis, in vitro and first in vivo evaluation of a new matrix metalloproteinase inhibitor based on γ-fluorinated α-sulfonylaminohydroxamic acid

EJNMMI radiopharmacy and chemistry, 2018-07, Vol.3 (1), p.10-10, Article 10

2018

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[18F]GP1, a novel PET tracer investigated for the detection of thrombi in LVADs and for the diagnosis of valve thrombosis

Nuclear medicine and biology, 2023-11, Vol.126-127, p.108436, Article 108436

2023

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P-186 - Cyclotron production of gallium-68 from liquid target: routine production of 68Ga-labelled radiotracers

Nuclear medicine and biology, 2022-05, Vol.108-109, p.S151-S151

2022

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Cyclotron production of gallium-68 from liquid target: routine production of 68Ga-labelled radiotracers

Nuclear medicine and biology, 2022-05, Vol.108-109, p.S151

2022

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P-028 - GMP-compliant radiosynthesis of [18F]GP1 for the detection of thrombi

Nuclear medicine and biology, 2022-05, Vol.108-109, p.S66-S66

2022

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GMP-compliant radiosynthesis of [18F]GP1 for the detection of thrombi

Nuclear medicine and biology, 2022-05, Vol.108-109, p.S66

2022

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Synthesis and evaluation of a [18F]BODIPY-labeled caspase-inhibitor

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (7), p.2167-2176

2017

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Radiolabeled Selective Matrix Metalloproteinase 13 (MMP-13) Inhibitors: (Radio)Syntheses and in Vitro and First in Vivo Evaluation

Journal of medicinal chemistry, 2017-01, Vol.60 (1), p.307-321

2017

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Development of symmetric O-BODIPYs with different optical properties as building blocks for the synthesis of ligands for multimodal imaging

Dyes and pigments, 2018-11, Vol.158, p.88-96

2018

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Noninvasive In Vivo Coronary Artery Thrombus Imaging

JACC. Cardiovascular imaging, 2023-06, Vol.16 (6), p.820-832

2023

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Facile synthesis of a,a-difluoroalkyl aryl thioethers and their oxidative desulfurization-fluorination to trifluorides

Journal of fluorine chemistry, 2010-09, Vol.131 (9), p.942-950

2010

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Inverse 1,2,3-Triazole-1-yl-ethyl Substituted Hydroxamates as Highly Potent Matrix Metalloproteinase Inhibitors: (Radio)synthesis, in Vitro and First in Vivo Evaluation

Journal of medicinal chemistry, 2013-09, Vol.56 (17), p.6858-6870

2013

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A New Class of Highly Potent Matrix Metalloproteinase Inhibitors Based on Triazole-Substituted Hydroxamates: (Radio)Synthesis and in Vitro and First in Vivo Evaluation

Journal of medicinal chemistry, 2012-05, Vol.55 (10), p.4714-4727

2012

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Facile synthesis of α,α-difluoroalkyl aryl thioethers and their oxidative desulfurization–fluorination to trifluorides

Journal of fluorine chemistry, 2010-09, Vol.131 (9), p.942-950

2010

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Oxidative desulfurization-fluorination of thioethers. Application for the synthesis of fluorinated nitrogen containing building blocksDedicated to the 10th Anniversary of the RSC Fluorine Group. This publication is part of the web themed issue on fluorine chemistry.CCDC reference number 788179. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c0ob00560f

2010-12

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Radiolabeled hydroxamate-based matrix metalloproteinase inhibitors: How chemical modifications affect pharmacokinetics and metabolic stability

Nuclear medicine and biology, 2016-07, Vol.43 (7), p.424-437

2016

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Peptide Beacons: A New Design for Polypeptide-Based Optical Biosensors

Bioconjugate chemistry, 2007-05, Vol.18 (3), p.607-609

2007

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Synthesis of Geminal Difluorides by Oxidative Desulfurization−Difluorination of Alkyl Aryl Thioethers with Halonium Electrophiles in the Presence of Fluorinating Reagents and Its Application for 18F-Radiolabeling

Journal of organic chemistry, 2010-09, Vol.75 (18), p.6086-6095

2010

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Synthesis of Geminal Difluorides by Oxidative Desulfurization−Difluorination of Alkyl Aryl Thioethers with Halonium Electrophiles in the Presence of Fluorinating Reagents and Its Application for 18 F-Radiolabeling

Journal of organic chemistry, 2010-09, Vol.75 (18), p.6086-6095

2010

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Fluoro-Pummerer rearrangement and analogous reactions

The Gordian Knot 2.0 - Decentralized production of radiopharmaceuticals

GMP-Compliant Radiosynthesis of [18F]GP1, a Novel PET Tracer for the Detection of Thrombi

Optimized Treatment and Recovery of Irradiated [18O]-Water in the Production of [18F]-Fluoride

Oxidative desulfurization-fluorination of thioethers. Application for the synthesis of fluorinated nitrogen containing building blocks

Synthesis, radiosynthesis, in vitro and first in vivo evaluation of a new matrix metalloproteinase inhibitor based on γ-fluorinated α-sulfonylaminohydroxamic acid

[18F]GP1, a novel PET tracer investigated for the detection of thrombi in LVADs and for the diagnosis of valve thrombosis

P-186 - Cyclotron production of gallium-68 from liquid target: routine production of 68Ga-labelled radiotracers

Cyclotron production of gallium-68 from liquid target: routine production of 68Ga-labelled radiotracers

P-028 - GMP-compliant radiosynthesis of [18F]GP1 for the detection of thrombi

GMP-compliant radiosynthesis of [18F]GP1 for the detection of thrombi

Synthesis and evaluation of a [18F]BODIPY-labeled caspase-inhibitor

Radiolabeled Selective Matrix Metalloproteinase 13 (MMP-13) Inhibitors: (Radio)Syntheses and in Vitro and First in Vivo Evaluation

Development of symmetric O-BODIPYs with different optical properties as building blocks for the synthesis of ligands for multimodal imaging

Noninvasive In Vivo Coronary Artery Thrombus Imaging

Facile synthesis of a,a-difluoroalkyl aryl thioethers and their oxidative desulfurization-fluorination to trifluorides

18F-GP1 Positron Emission Tomography and Bioprosthetic Aortic Valve Thrombus

Inverse 1,2,3-Triazole-1-yl-ethyl Substituted Hydroxamates as Highly Potent Matrix Metalloproteinase Inhibitors: (Radio)synthesis, in Vitro and First in Vivo Evaluation

A New Class of Highly Potent Matrix Metalloproteinase Inhibitors Based on Triazole-Substituted Hydroxamates: (Radio)Synthesis and in Vitro and First in Vivo Evaluation

Facile synthesis of α,α-difluoroalkyl aryl thioethers and their oxidative desulfurization–fluorination to trifluorides

Radiolabeled hydroxamate-based matrix metalloproteinase inhibitors: How chemical modifications affect pharmacokinetics and metabolic stability

Peptide Beacons: A New Design for Polypeptide-Based Optical Biosensors

Synthesis of Geminal Difluorides by Oxidative Desulfurization−Difluorination of Alkyl Aryl Thioethers with Halonium Electrophiles in the Presence of Fluorinating Reagents and Its Application for 18F-Radiolabeling

Synthesis of Geminal Difluorides by Oxidative Desulfurization−Difluorination of Alkyl Aryl Thioethers with Halonium Electrophiles in the Presence of Fluorinating Reagents and Its Application for 18 F-Radiolabeling

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