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Constantin Mamat - Publications

Affiliations: 
1998-2007 Chemistry Universität Rostock, Rostock, Mecklenburg-Vorpommern, Germany 
 2007- Radiopharmacy Helmholtz-Zentrum Dresden-Rossendorf / TU Dresden 
Area:
Organic Chemistry, Coordination Chemistry, Radiopharmaceutical Chemistry
Website:
http://www.hzdr.de/db/Cms?pNid=727
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45 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Miederer M, Benešová-Schäfer M, Mamat C, Kästner D, Pretze M, Michler E, Brogsitter C, Kotzerke J, Kopka K, Scheinberg DA, McDevitt MR. Alpha-Emitting Radionuclides: Current Status and Future Perspectives. Pharmaceuticals (Basel, Switzerland). 17. PMID 38256909 DOI: 10.3390/ph17010076  0.663
2021 Mamat C, Jentschel C, Köckerling M, Steinbach J. Strategic Evaluation of the Traceless Staudinger Ligation for Radiolabeling with the Tricarbonyl Core. Molecules (Basel, Switzerland). 26. PMID 34771038 DOI: 10.3390/molecules26216629  0.522
2020 Pretze M, Neuber C, Kinski E, Belter B, Köckerling M, Caflisch A, Steinbach J, Pietzsch J, Mamat C. Synthesis, radiolabelling and initial biological characterisation of F-labelled xanthine derivatives for PET imaging of Eph receptors. Organic & Biomolecular Chemistry. 18: 3104-3116. PMID 32253415 DOI: 10.1039/D0Ob00391C  0.748
2019 Gott M, Yang P, Kortz U, Stephan H, Pietzsch HJ, Mamat C. A Ra-labeled polyoxopalladate as a putative radiopharmaceutical. Chemical Communications (Cambridge, England). PMID 31197298 DOI: 10.1039/c9cc02587a  0.68
2019 Reissig F, Hübner R, Steinbach J, Pietzsch H, Mamat C. Facile preparation of radium-doped, functionalized nanoparticles as carriers for targeted alpha therapy Inorganic Chemistry Frontiers. 6: 1341-1349. DOI: 10.1039/C9QI00208A  0.471
2019 Bauer D, Reissig F, Pietzsch H, steinbach J, Mamat C. Calixarene Based Ligands for Radium and Barium Journal of Medical Imaging and Radiation Sciences. 50: S111. DOI: 10.1016/j.jmir.2019.11.123  0.413
2019 Reissig F, Bauer D, Pietzsch H, Steinbach J, Mamat C. Synthesis and Functionalization of Radium-doped Barium Sulfate Nanoparticles Journal of Medical Imaging and Radiation Sciences. 50: S110-S111. DOI: 10.1016/j.jmir.2019.11.122  0.452
2019 Bauer D, Reissig F, Pietzsch H, steinbach J, Mamat C. Calixarene Based Ligands for Radium and Barium Journal of Medical Imaging and Radiation Sciences. 50: S39. DOI: 10.1016/J.JMIR.2019.03.118  0.413
2019 Reissig F, Bauer D, Pietzsch H, Steinbach J, Mamat C. Synthesis and Functionalization of Radium-doped Barium Sulfate Nanoparticles Journal of Medical Imaging and Radiation Sciences. 50: S38. DOI: 10.1016/J.JMIR.2019.03.117  0.452
2018 Bauer D, Gott M, Steinbach J, Mamat C. Chelation of heavy group 2 (radio)metals by p-tert-butylcalix[4]arene-1,3-crown-6 and logK determination via NMR. Spectrochimica Acta. Part a, Molecular and Biomolecular Spectroscopy. 199: 50-56. PMID 29567522 DOI: 10.1016/j.saa.2018.03.029  0.712
2018 Mamat C, Gott M, Steinbach J. Recent progress using the Staudinger ligation for radiolabeling applications. Journal of Labelled Compounds & Radiopharmaceuticals. 61: 165-178. PMID 28895180 DOI: 10.1002/jlcr.3562  0.757
2017 Wiemer J, Steinbach J, Pietzsch J, Mamat C. Preparation of a novel radiotracer targeting the EphB4 receptor via radiofluorination using spiro azetidinium salts as precursor. Journal of Labelled Compounds & Radiopharmaceuticals. 60: 489-498. PMID 28561530 DOI: 10.1002/jlcr.3526  0.555
2017 Mamat C, Pretze M, Gott M, Köckerling M. Correction: Synthesis, dynamic NMR characterization and XRD studies of novel ,'-substituted piperazines for bioorthogonal labeling. Beilstein Journal of Organic Chemistry. 13: 301-302. PMID 28326138 DOI: 10.3762/bjoc.13.32  0.744
2016 Mamat C, Pretze M, Gott M, Köckerling M. Synthesis, dynamic NMR characterization and XRD studies of novel ,'-substituted piperazines for bioorthogonal labeling. Beilstein Journal of Organic Chemistry. 12: 2478-2489. PMID 28144316 DOI: 10.3762/bjoc.12.242  0.755
2016 Gott M, Steinbach J, Mamat C. Erratum to: the radiochemical and radiopharmaceutical applications of radium Open Chemistry. 14: 130. DOI: 10.1515/chem-2016-0012  0.718
2016 Gott M, Steinbach J, Mamat C. The Radiochemical and Radiopharmaceutical Applications of Radium Open Chemistry. 14: 118-129. DOI: 10.1515/chem-2016-0011  0.722
2015 Ebert K, Wiemer J, Caballero J, Köckerling M, Steinbach J, Pietzsch J, Mamat C. Development of indazolylpyrimidine derivatives as high-affine EphB4 receptor ligands and potential PET radiotracers. Bioorganic & Medicinal Chemistry. 23: 6025-35. PMID 26189032 DOI: 10.1016/j.bmc.2015.06.040  0.572
2015 Xie F, Bergmann R, Kniess T, Deuther-Conrad W, Mamat C, Neuber C, Liu B, Steinbach J, Brust P, Pietzsch J, Jia H. 18F-labeled 1,4-Dioxa-8-azaspiro[4.5]decane Derivative: Synthesis and Biological Evaluation of a Sigma-1 Receptor Radioligand with Low Lipophilicity as Potent Tumor Imaging Agent. Journal of Medicinal Chemistry. PMID 26090686 DOI: 10.1021/Acs.Jmedchem.5B00593  0.54
2015 Xie F, Kniess T, Neuber C, Deuther-Conrad W, Mamat C, Lieberman BP, Liu B, Mach RH, Brust P, Steinbach J, Pietzsch J, Jia H. Novel indole-based sigma-2 receptor ligands: synthesis, structure-affinity relationship and antiproliferative activity Medchemcomm. 6: 1093-1103. DOI: 10.1039/C5Md00079C  0.486
2014 Pretze M, Mosch B, Bergmann R, Steinbach J, Pietzsch J, Mamat C. Radiofluorination and first radiopharmacological characterization of a SWLAY peptide-based ligand targeting EphA2. Journal of Labelled Compounds & Radiopharmaceuticals. 57: 660-5. PMID 25263640 DOI: 10.1002/jlcr.3237  0.74
2013 Pretze M, Pietzsch D, Mamat C. Recent trends in bioorthogonal click-radiolabeling reactions using fluorine-18. Molecules (Basel, Switzerland). 18: 8618-65. PMID 23881051 DOI: 10.3390/molecules18078618  0.731
2013 Pretze M, Kuchar M, Bergmann R, Steinbach J, Pietzsch J, Mamat C. An efficient bioorthogonal strategy using CuAAC click chemistry for radiofluorinations of SNEW peptides and the role of copper depletion. Chemmedchem. 8: 935-45. PMID 23559494 DOI: 10.1002/cmdc.201300053  0.756
2013 Heldt J, Kerzendörfer O, Mamat C, Starke F, Pietzsch H, Steinbach J. Synthesis of Short and Versatile Heterobifunctional Linkers for Conjugation of Bioactive Molecules with (Radio-)Labels Synlett. 24: 432-436. DOI: 10.1055/S-0032-1318198  0.522
2013 Pretze M, Mamat C. Automated preparation of [18F]AFP and [18F]BFP: Two novel bifunctional 18F-labeling building blocks for Huisgen-click Journal of Fluorine Chemistry. 150: 25-35. DOI: 10.1016/J.JFLUCHEM.2013.02.028  0.688
2013 Mamat C, Langer P. Condensation of the dianion of ethyl acetoacetate with perfluoroalkyl iodides. Application to the synthesis of 3-perfluoroalkylsalicylic acids Monatshefte FüR Chemie - Chemical Monthly. 144: 1057-1061. DOI: 10.1007/s00706-013-0985-8  0.394
2013 Reimann S, Bunescu A, Petrosyan A, Sharif M, Erfle S, Mamat C, Ghochikyan TV, Saghyan AS, Spannenberg A, Villinger A, Langer P. Regioselective synthesis of trichloromethyl-substituted salicylates and cyclohexenones by one-pot cyclizations of 1,3-bis(trimethylsilyloxy)buta-1,3- dienes Helvetica Chimica Acta. 96: 1955-1967. DOI: 10.1002/hlca.201200595  0.432
2013 Mamat C, Langer P. ChemInform Abstract: Condensation of the Dianion of Ethyl Acetoacetate with Perfluoroalkyl Iodides. Application to the Synthesis of 3-Perfluoroalkylsalicylic Acids. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201342058  0.404
2011 Pretze M, Grosse-Gehling P, Mamat C. Cross-coupling reactions as valuable tool for the preparation of PET radiotracers. Molecules (Basel, Switzerland). 16: 1129-65. PMID 21270732 DOI: 10.3390/molecules16021129  0.711
2011 Grosse-Gehling P, Wuest F, Peppel T, Köckerling M, Mamat C. 1-(3-[18F]fluoropropyl)piperazines as model compounds for the radiofluorination of pyrido[2,3-d]pyrimidines Radiochimica Acta. 99: 365-373. DOI: 10.1524/ract.2011.1834  0.304
2011 Mamat C, Franke M, Peppel T, Köckerling M, Steinbach J. Synthesis, structure determination, and (radio-)fluorination of novel functionalized phosphanes suitable for the traceless Staudinger ligation Tetrahedron. 67: 4521-4529. DOI: 10.1016/J.TET.2011.04.091  0.507
2010 Pretze M, Flemming A, Kockerling M, Mamat C. Synthesis and Radiofluorination of Iodophenyl Esters as Tool for the Traceless Staudinger Ligation Zeitschrift FüR Naturforschung B. 65: 1128-1136. DOI: 10.1515/znb-2010-0912  0.716
2010 Pretze M, Wuest F, Peppel T, Köckerling M, Mamat C. The traceless Staudinger ligation with fluorine-18: a novel and versatile labeling technique for the synthesis of PET-radiotracers Tetrahedron Letters. 51: 6410-6414. DOI: 10.1016/J.TETLET.2010.09.134  0.714
2010 Pretze M, Flemming A, Koeckerling M, Mamat C. ChemInform Abstract: Synthesis and Radiofluorination of Iodophenyl Esters as Tool for the Traceless Staudinger Ligation. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201104081  0.701
2009 Mamat C, Reinke H, Langer P. NMR Studies and Crystal Structure Determinations of CF3 Group-containing Bicyclic Phenolates Zeitschrift FüR Naturforschung B. 64: 423-426. DOI: 10.1515/znb-2009-0411  0.333
2009 Mamat C, Flemming A, Köckerling M, Steinbach J, Wuest F. Synthesis of Benzoate-Functionalized Phosphanes as Novel Building Blocks for the Traceless Staudinger Ligation Synthesis. 2009: 3311-3321. DOI: 10.1055/S-0029-1216947  0.499
2008 Langer P, Lubbe M, Mamat C. Regioselective Synthesis of Rare 3-Halomethylphenols Based on Formal [3+3] Cyclizations of 1,3-Bis(trimethylsilyloxy)-1,3-butadienes Synlett. 2008: 1684-1686. DOI: 10.1055/S-2008-1077877  0.408
2008 Mamat C, Pundt T, Tam Dang TH, Klassen R, Reinke H, Köckerling M, Langer P. One-Pot Synthesis of Functionalized 3-(Trifluoromethyl)phenols by [3+3] Cyclization of 1,3-Bis(silyl enol ethers) with α,β-Unsaturated Trifluoromethyl Ketones European Journal of Organic Chemistry. 2008: 492-502. DOI: 10.1002/EJOC.200700801  0.354
2008 Lubbe M, Mamat C, Langer P. ChemInform Abstract: Regioselective Synthesis of Rare 3-Halomethylphenols Based on Formal [3 + 3] Cyclizations of 1,3-Bis(trimethylsilyloxy)-1,3-butadienes. Cheminform. 39. DOI: 10.1002/CHIN.200844069  0.415
2008 Mamat C, Pundt T, Dang THT, Klassen R, Reinke H, Koeckerling M, Langer P. ChemInform Abstract: One-Pot Synthesis of Functionalized 3-(Trifluoromethyl)phenols by [3 + 3] Cyclization of 1,3-Bis(silyl enol ethers) with α,β-Unsaturated Trifluoromethyl Ketones. Cheminform. 39. DOI: 10.1002/CHIN.200819061  0.359
2007 Mamat C, Büttner S, Trabhardt T, Fischer C, Langer P. Regioselective synthesis of 5-alkylsalicylates, 5-alkyl-2-hydroxy-acetophenones, and 5-alkyl-2-hydroxy-benzophenones by [3 + 3] cyclization of 1,3-bis(silyl enol ethers) with 2-alkyl-1,1,3,3-tetraethoxypropanes. The Journal of Organic Chemistry. 72: 6273-5. PMID 17616148 DOI: 10.1002/CHIN.200751095  0.419
2007 Lubbe M, Mamat C, Fischer C, Langer P. Synthesis of 6-(perfluoroalkyl)salicylates by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-ethoxy-1-(perfluoroalkyl)prop-2-en-1-ones Tetrahedron. 63: 413-418. DOI: 10.1016/J.TET.2006.10.062  0.436
2007 Lubbe M, Mamat C, Fischer C, Langer P. Synthesis of 6-(Perfluoroalkyl)salicylates by [3 + 3] Cyclization of 1,3-Bis(silyl enol ethers) with 3-Ethoxy-1-(perfluoroalkyl)prop-2-en-1-ones. Cheminform. 38. DOI: 10.1002/CHIN.200721068  0.436
2006 Mamat C, Hein M, Miethchen R. Fluorinated acyclo-C-nucleoside analogues from glycals in two steps. Carbohydrate Research. 341: 1758-63. PMID 16442508 DOI: 10.1016/j.carres.2006.01.011  0.733
2006 Mamat C, Pundt T, Schmidt A, Langer P. Regioselective synthesis of 2-acetyl- and 2-alkoxycarbonyl-3-(trifluoromethyl)phenols by [3+3] cyclization of 1,3-bis-silyl enol ethers with 4-ethoxy- and 4-silyloxy-1,1,1-trifluoroalk-3-en-2-ones Tetrahedron Letters. 47: 2183-2185. DOI: 10.1016/J.TETLET.2006.01.111  0.432
2006 Mamat C, Pundt T, Schmidt A, Langer P. Regioselective Synthesis of 2-Acetyl- and 2-Alkoxycarbonyl-3-(trifluoromethyl)phenols by [3 + 3] Cyclization of 1,3-Bis-silyl Enol Ethers with 4-Ethoxy- and 4-Silyloxy-1,1,1-trifluoroalk-3-en-2-ones. Cheminform. 37. DOI: 10.1002/CHIN.200627070  0.432
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