Journal of Labelled Compounds & Radiopharmaceuticals

Papers
(The TQCC of Journal of Labelled Compounds & Radiopharmaceuticals is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Use of radioiodine in nuclear medicine—A brief overview23
Radiosynthesis and quality control testing of the tau imaging positron emission tomography tracer [18F]PM‐PBB3 for clinical applications16
Radioiodination of balsalazide, bioevaluation, and characterization as a highly selective radiotracer for imaging of ulcerative colitis in mice13
Production of [89Zr]Oxinate4 and cell radiolabeling for human use12
Automated radiosynthesis of [68Ga]Ga‐PSMA‐11 and [177Lu]Lu‐PSMA‐617 on the iPHASE MultiSyn module for clinical applications11
Strategies for designing novel positron emission tomography (PET) radiotracers to cross the blood–brain barrier8
Fully automated production of the fibroblast activation protein radiotracer [18F]FAPI‐748
Review: Self‐radiolysis of compounds containing tritium and carbon‐147
Polyethylene oxide–polyacrylic acid–folic acid (PEO‐PAAc) nanogel as a99mTc targeting receptor for cancer diagnostic imaging7
Copper‐mediated radioiodination reaction through aryl boronic acid or ester precursor and its application to direct radiolabeling of a cyclic peptide7
Peptides for trans‐blood–brain barrier delivery6
A practical approach to the optimization of positron emission tomography imaging agents for the central nervous system6
Development of an automated production process of [64Cu][Cu (ATSM)] for positron emission tomography imaging and theranostic applications6
Preclinical evaluation of anti‐VEGFR2 monoclonal antibody ramucirumab labelled with zirconium‐89 for tumour imaging5
Evaluating N‐difluoromethyltriazolium triflate as a precursor for the synthesis of high molar activity [18F]fluoroform5
Carbon‐11 carboxylation of terminal alkynes with [11C]CO24
Synthesis and automated fluorine‐18 radiolabeling of new PSMA‐617 derivatives with a CuAAC radiosynthetic approach4
Synthesis of [H‐3]‐ and [C‐14]‐labeled elagolix4
Synthesis of deuterium‐labeled cinnamic acids: Understanding the volatile benzenoid pathway in the flowers of the Japanese loquat Eriobotrya japonica4
Preparation, Characterization, and Radiolabeling of Anti‐HER2 scFv With Technetium Tricarbonyl and Stability Studies4
Detailed radiosynthesis of [18F]mG4P027 as a positron emission tomography radiotracer for mGluR44
The impact of radiochemistry in drug projects: The use of C‐14 label in the AZD8529, AZD7325, and AZD6280 projects4
Synthesis and analysis of isotopically stable labeled nitrosamines as mass spectrometry standards for drug impurity quality control3
A practical and environmentally friendly protocol for synthesis of α‐deuterated carboxylic acids3
Exploration of alcohol‐enhanced Cu‐mediated radiofluorination toward practical labeling3
Carbon 14 synthesis of glycine transporter 1 inhibitor Iclepertin (BI 425809) and its major metabolites3
Comparison of three different methods in [68Ga]Ga‐PSMA11 radiolabeling3
Isotopically labelled compounds in research projects of life sciences3
Highly selective catalytic transfer hydrodeuteration of cyclic alkenes3
Luminescence enhancement by deuterium3
The inverse electron demand Diels–Alder cycloaddition with carbon‐11 and fluorine‐18: A gateway to pretargeted imaging across the blood–brain barrier3
Synthesis of [13C6]‐ibrutinib3
An improved one‐pot preparation of [18F]FMISO based on solid phase extraction purification: Pitfalls on the analytical method reported in the Ph.Eur.'s monograph3
Automated radiosynthesis of 1‐(2‐[18F]fluoroethyl)‐L‐tryptophan ([18F]FETrp) for positron emission tomography (PET) imaging of cancer in humans3
Development of a novel [18F]fluorobenzyl derivative of the AT1 receptor antagonist Candesartan3
Synthesis of 13C‐labelled cutin and suberin monomeric dicarboxylic acids of the general formula HO213C‐(CH2)n13CO2H (n<3
An optimized radiosynthesis of [18F]DK222, a PET radiotracer for imaging PD‐L12
Radiosynthesis of 3H‐ and 14C‐labeled Veliparib2
Good manufacturing procedure production of [18F]SynVesT‐1, a radioligand for in vivo positron emission tomography imaging of synaptic vesicle glycoprotein 2A2
Novel developed HPLC analyses of [68Ga]Ga/[177Lu]Lu‐EDTMP and [68Ga]Ga/[177Lu]Lu‐DOTA‐Zoledronate2
An efficient and general method for the synthesis of stable isotope deuterium labeled phthalate esters2
Process validation, current good manufacturing practice production, dosimetry, and toxicity studies of the carbonic anhydrase IX imaging agent [111In]In‐XYIMSR‐01 for phase I regulatory app2
Development of a 68Ga‐labelled PET tracer for carbonic anhydrase IX‐overexpressed tumors using the artificial sweetener saccharin2
Benzylic deuteration of alkylnitroaromatics via amine‐base catalysed exchange with deuterium oxide2
Enzymatic synthesis of halogen derivatives of L‐phenylalanine and phenylpyruvic acid stereoselectively labeled with hydrogen isotopes in the side chain2
High‐yield synthesis of a tau PET radioligand and its nonradioactive ligand using an alternative protection and deprotection strategy2
Automated synthesis of (R)‐[18F]MH.MZ on the iPhase Flexlab reaction platform2
Automated radiosynthesis of the adenosine A2A receptor‐targeting radiotracer [18F]FLUDA2
Development of radiotracers for riboflavin transporter 3 imaging in diseases—A brief overview2
Improved protocol for the radiosynthesis of [18F]FTC‐146: A potent and selective sigma‐1 receptor radioligand2
Synthesis of [2H5]baricitinib via [2H5]ethanesulfonyl chloride2
Preparation, quality control, and biodistribution assessment of [111In]In‐DOTA‐PR81 in BALB/c mice bearing breast tumors2
An updated synthesis of N1′‐([11C]methyl)naltrindole for positron emission tomography imaging of the delta opioid receptor2
Development and physicochemical characterization of a biodegradable microspheres formulation loaded with samarium‐153 and doxorubicin for chemo‐radioembolization of liver tumours2
Fluorine‐18 labeled aldehydes as prosthetic groups for oxime coupling with a FVIIa protein2
Copper‐mediated nucleophilic radiofluorination of [18F]β‐CFT for positron emission tomography imaging of dopamine transporter2
Automated radiosynthesis of [11C]MTP38—a phosphodiesterase 7 imaging tracer—using [11C]hydrogen cyanide for clinical applications2
Synthesis of a dual carbon‐14‐labeled calcitonin gene‐related peptide receptor antagonist for use in a human absorption–distribution–metabolism–elimination study2
Mild and selective hydrogen–deuterium exchange for aromatic hydrogen of amines1
[18F]Fluoropyridine‐losartan: A new approach toward human Positron Emission Tomography imaging of Angiotensin II Type 1 receptors1
Issue Information1
Research on preparation and in vitro evaluation of the dendrimerpeptide nuclear acid conjugate for amplification pretargeting1
Tritium hydrogen‐isotope exchange with electron‐poor tertiary benzenesulfonamide moiety; application in late‐stage labeling of T09013171
Determination of isotope abundance for deuterium‐labeled compounds by quantitative 1H NMR + 2H NMR1
An Improved HPLC Separation Method for TSPO Radioligand [11C]ER176 Clinical Production1
Simplified and accessible [18F]F‐AraG synthesis procedure for preclinical PET1
Fully Automated Cassette‐Based Synthesis of 2‐Deoxy‐2‐[18F]Fluorocellobiose Using Trasis AllInOne Module1
In vivo and in vitro binding of [125I]I‐R‐(+)‐TISCH: A dopamine D1 receptor ligand for studying pancreatic β‐cell mass1
Synthesis of 13C‐labeled parabens from isotopically enriched phenols using the Houben–Hoesch reaction1
A facile synthesis of isotope labeled acylcarnitines1
An improved synthesis of [18F]VAT and its precursor1
Preparation and biological evaluation of radioiodine‐labeled triphenylphosphine derivatives as mitochondrial targeting probes1
Total synthesis of [13C2]‐labeled phytosiderophores of the mugineic and avenic acid families1
Highly effective liquid and solid phase extraction methods to concentrate radioiodine isotopes for radioiodination chemistry1
Radiosynthesis and validation of [18F]fluoroestradiol in a Synthra plus research platform for use in routine clinical practice1
Synthesis of beta‐site amyloid precursor protein‐cleaving enzyme 1 inhibitors BI 1147560 and BI 1181181 labeled with carbon‐14 and deuterium1
Exploring the enzyme‐catalyzed synthesis of isotope labeled cyclopropanes1
The impact of zirconium‐89 solution formulation on the efficiency of [89Zr]Zr‐deferoxamine synthesis1
Synthesis and radiolabeling of a polar [125I]I‐1,2,4,5‐tetrazine1
Automated radiochemical synthesis of pharmaceutical grade [18F]FLT using 3‐N‐Boc‐5′‐O‐dimethoxytrityl‐3′‐O‐nosyl‐thymidine precursor and its Sep‐Pak® purification employing selective elutio1
RO6807936 as a novel positron emission tomography (PET) radiotracer for in vitro and in vivo visualization and quantification of beta‐site amyloid precursor protein cleaving enzyme (BACE1) in the rode1
The synthesis of deuteriated tri‐tert‐butyl phosphine1
Low‐scale syringe‐made synthesis of 15N‐labeled oligonucleotides1
Efficient synthesis of carbon‐14 labeled metabolites of the strobilurin fungicide mandestrobin using biomimetic iron‐porphyrin catalyzed oxidation1
A comparative study on Suzuki‐type 11C‐methylation of aromatic organoboranes performed in two reaction media1
Synthesis of [4S2H]NADH, [4R2H]NADH, [4‐2H2]NADH and [4‐2H]NAD+ cofactors through heterogeneous biocatalysis in heavy 1
Preliminary PET imaging of [11C]evobrutinib in mouse models of colorectal cancer, SARS‐CoV‐2, and lung damage: Radiosynthesis via base‐aided palladium‐NiXantphos‐mediated 11C‐car1
Ultra‐fast liquid chromatography method coupled with ultraviolet detection to quantify dimethylsulfoxide, dimethylformamide and dimethylacetamide in short half‐lives radiopharmaceuticals1
Synthesis of tritium labeled 30‐KDa PEG and conjugation to form [3H]Pegbelfermin1
Site‐specifically radiolabeled nanobodies for imaging blood‐brain barrier penetration and targeting in the brain1
Small‐scale two‐dimensional liquid chromatography for a preparative re‐purification of a highly labile tritium‐labeled compound1
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