PUBLICATIONS

[*corresponding author, ^#equal contributions]

2023

Houszka, N.; Mikula, H.; Svatunek, D.; Substituent Effects in Bioorthogonal Diels–Alder Reactions of 1,2,4,5-Tetrazines.
Chem. Eur. J. 2023, accepted manuscript, doi: 10.1002/chem.202300345

Pavicich, M. A.;De Boevre, M.; Vidal, A.; Mikula, H.; Warth, B.; Marko, D.; De Saeger, S.; Patriarca, A., Natural Occurrence, Exposure Assessment & Risk Characterization of Alternaria Mycotoxins in Apple By-Products in Argentina.
Expo. Health 2023, accepted manuscript, doi: 10.1007/s12403-023-00544-1

Kuba, W.; Sohr, B.; Keppel, P.; Svatunek, D.; Humhal, V.; Stöger, B.; Goldeck, M.; Carlson, J. C. T.; Mikula, H.*, Oxidative Desymmetrization Enables the Concise Synthesis of a trans-Cyclooctene Linker for Bioorthogonal Bond-Cleavage.
Chem. Eur. J. 2023, 29, e202203069, doi: 10.1002/chem.202203069

Shalgunov, V.; van den Broek, S. L.; Vang Andersen, I.; García-Vázquez, R.; Raval, R. G.; Palner, M.; Mori, Y.; Schäfer, G.; Herrmann, B.; Mikula, H.; Beschorner, N.; Nedergaard, M.; Syvänen, S.; Barz, M.; Knudsen, G. M.; Battisti, U. M.; Herth, M. M., Pretargeted imaging beyond the blood–brain barrier. RSC Med. Chem. 2023, 14, 444-453, DOI: 10.1039/D2MD00360K

2022

Keppel, P.; Sohr, B.; Kuba, W.; Goldeck, M.; Skrinjar, P.; Carlson, J. C. T.; Mikula, H.*, Tetrazine-Triggered Bioorthogonal Cleavage of trans-Cyclooctene-Caged Phenols Using a Minimal Self-Immolative Linker Strategy.
ChemBioChem 2022, 23, e202200363, doi: 10.1002/cbic.202200363

Ko, J.; Wilkovitsch, M.; Oh, J.; Kohler, R. H.; Bolli, E.; Pittet, M. J.; Vinegoni, C.; Sykes, D. B.; Mikula, H.; Weissleder, R.; Carlson, J. C. T., Spatiotemporal multiplexed immunofluorescence imaging of living cells and tissues with bioorthogonal cycling of fluorescent probes.
Nature Biotechnol. 2022, 40, 1654–1662, doi: 10.1038/s41587-022-01339-6

Svatunek, D.; Wilkovitsch, M.; Hartmann, L.; Houk, K. N.; Mikula, H.*, Uncovering the Key Role of Distortion in Bioorthogonal Tetrazine Tools that Defy the Reactivity/Stability Tradeoff.
J. Am. Chem. Soc. 2022, 144, 8171-8177, doi: 10.1021/jacs.2c01056

Ng, T. S. C.; Hu, H.; Kronister, S.; Lee, C.; Li, R.; Gerosa, L.; Stopka, S. A.; Burgenske, D. M.; Khurana, I.; Regan, M. S.; Vallabhaneni, S.; Putta, N.; Scott, E.; Matvey, D.; Giobbie-Hurder, A.; Kohler, R. H.; Sarkaria, J. N.; Parangi, S.; Sorger, P. K.; Agar, N. Y. R.; Jacene, H. A.; Sullivan, R. J.; Buchbinder, E.; Mikula, H.; Weissleder, R.; Miller, M. A., Overcoming differential tumor penetration of BRAF inhibitors using computationally guided combination therapy.
Science Adv. 2022, 8, eabl6339, doi: 10.1126/sciadv.abl6339

Battisti, U. M.; García-Vázquez, R.; Svatunek, D.; Herrmann, B.; Löffler, A.; Mikula, H.; Herth, M. M., Synergistic Experimental and Computational Investigation of the Bioorthogonal Reactivity of Substituted Aryltetrazines.
Bioconjugate Chem. 2022, 33, 608-624, doi: 10.1021/acs.bioconjchem.2c00042

2021

Li, R.; Ng, T. S. C.; Wang, S. J.; Prytyskach, M.; Rodell, C. B.; Mikula, H.; Kohler, R. H.; Garlin, M. A.; Lauffenburger, D. A.; Parangi, S.; Dinulescu, D. M.; Bardeesy, N.; Weissleder, R.; Miller, M. A., Therapeutically reprogrammed nutrient signalling enhances nanoparticulate albumin bound drug uptake and efficacy in KRAS-mutant cancer.
Nature Nanotechnol. 2021, 16, 830-839, doi: 10.1038/s41565-021-00897-1

Kuba, W.; Wilkovitsch, M.; Carlson, J. C. T.; Mikula, H., Tetrazine-based cycloadditions in click chemistry.
Science of Synthesis 2021/4: Click Chemistry, book chapter, doi: 10.1055/sos-SD-235-00300

García-Vázquez, R.; Battisti, U. M.; Jørgensen, J. T.; Shalgunov, V.; Hvass, L.; Stares, D. L.; Petersen, I. N.; Crestey, F.; Löffler, A.; Svatunek, D.; Kristensen, J. L.; Mikula, H.; Kjaer, A.; Herth, M. M., Direct Cu-mediated aromatic 18F-labeling of highly reactive tetrazines for pretargeted bioorthogonal PET imaging.
Chem. Sci. 2021, 12, 11668-11675, doi: 10.1039/D1SC02789A

Battisti, U. M.; Bratteby, K.; Jørgensen, J. T.; Hvass, L.; Shalgunov, V.; Mikula, H.; Kjaer, A.; Herth, M. M., Development of the First Aliphatic 18F-Labeled Tetrazine Suitable for Pretargeted PET Imaging—Expanding the Bioorthogonal Tool Box.
J. Med. Chem. 2021, 64, 15297-15312, doi: 10.1021/acs.jmedchem.1c01326

Stéen, E. J. L.; Jørgensen, J. T.; Denk, C.; Battisti, U. M.; Nørregaard, K.; Edem, P. E.; Bratteby, K.; Shalgunov, V.; Wilkovitsch, M.; Svatunek, D.; Poulie, C. B. M.; Hvass, L.; Simón, M.; Wanek, T.; Rossin, R.; Robillard, M.; Kristensen, J. L.; Mikula, H.*; Kjaer, A.*; Herth, M. M.*, Lipophilicity and Click Reactivity Determine the Performance of Bioorthogonal Tetrazine Tools in Pretargeted In Vivo Chemistry.
ACS Pharmacol. Transl. Sci. 2021, 4, 824-833, doi: 10.1021/acsptsci.1c00007

2020

Schwarz, M.; Skrinjar, P.; Fink, M.; Kronister, S.; Mechtler, T.; Koukos, P. I.; Bonvin, A.; Kasper, D.; Mikula, H.*, A click-flipped enzyme substrate boosts the performance of the diagnostic screening for Hunter syndrome.
Chem. Sci. 2020, 11, 12671-12676, doi: 10.1039/D0SC04696E

Wilkovitsch, M.; Haider, M.; Sohr, B.; Herrmann, B.; Klubnick, J.; Weissleder, R.; Carlson, J. C. T.; Mikula, H.*, A Cleavable C₂-Symmetric trans-Cyclooctene Enables Fast and Complete Bioorthogonal Disassembly of Molecular Probes.
J. Am. Chem. Soc. 2020, 142, 19132-19141, doi: 10.1021/jacs.0c07922

Colón-Berríos, A. R.; McGinn, C. K.; Cavallari, M. R.; Bahamonde, J. A.; Yelavik, N.; Mikula, H.; Bintinger, J.; Kymissis, I., Improved Cyclohexanone Vapor Detection via Gravimetric Sensing.
IEEE J. Microelectromech. S. 2020, 5, 1253-1263, doi: 10.1109/JMEMS.2020.3010463

Johann, K.; Svatunek, D.; Seidl, C.; Rizzelli, S.; Bauer, T. A.; Braun, L.; Koynov, K.; Mikula, H.; Barz, M., Tetrazine- and trans-cyclooctene-functionalised polypept(o)ides for fast bioorthogonal tetrazine ligation.
Polymer Chem. 2020, 11, 4396-4407, doi: 10.1039/D0PY00375A

Pavicich, M. A.; De Boevre, M.; Vidal, A.; Iturmendi, F.; Mikula, H.; Warth, B.; Marko, D.; De Saeger, S.; Patriarca, A., Fate of free and modified Alternaria mycotoxins during the production of apple concentrates.
Food Control 2020, 118, 107388, doi: 10.1016/j.foodcont.2020.107388

Stéen, E. J. L.; Jørgensen, J. T.; Johann, K.; Nørregaard, K.; Sohr, B.; Svatunek, D.; Birke, A.; Shalgunov, V.; Edem, P. E.; Rossin, R.; Seidl, C.; Schmid, F.; Robillard, M. S.; Kristensen, J. L.; Mikula, H.; Barz, M.; Kjær, A.; Herth, M. M., Trans-Cyclooctene-Functionalized PeptoBrushes with Improved Reaction Kinetics of the Tetrazine Ligation for Pretargeted Nuclear Imaging. 
ACS Nano 2020, 14, 568-584, doi: 10.1021/acsnano.9b06905

Svatunek, D.; Eilenberger, G.; Denk, C.; Lumpi, D.; Hametner, C.; Allmaier, G.; Mikula, H.*, Live Monitoring of Strain‐Promoted Azide Alkyne Cycloadditions in Complex Reaction Environments by Inline ATR‐IR Spectroscopy.
Chem. Eur. J. 2020, 26, 9851-9854 (Young Chemists Issue), doi: 10.1002/chem.201905478

2019

Weber, J.; Svatunek, D.; Tegl, G.; Hametner, C.; Kosma, P.; Mikula, H.*, 2-O-Benzyloxycarbonyl protected glycosyl donors: a revival of carbonate-mediated anchimeric assistance for diastereoselective glycosylation.
Chem. Commun. 2019, 55, 12543-12546, doi: 10.1039/C9CC07194F

Kramer, S.; Svatunek, D.; Alberg, I.; Gräfen, B.; Schmitt, S.; Braun, L.; van Onzen, A. H. A. M.; Rossin, R.; Koynov, K.; Mikula, H.; Zentel, R., HPMA-Based Nanoparticles for Fast, Bioorthogonal iEDDA Ligation.
Biomacromolecules 2019, 20, 3786-3797, doi: 10.1021/acs.biomac.9b00868 

Denk, C.; Wilkovitsch, M.; Aneheim, E.; Herth, M. M.; Jensen, H.; Lindegren, H.; Mikula, H.*, Multifunctional clickable reagents for rapid bioorthogonal astatination and radio-crosslinking.
ChemPlusChem 2019, 84, 775-778 (Early Career Series), doi: 10.1002/cplu.201900114

Rosecker, V.; Denk, C.; Maurer, M.; Wilkovitsch, M.; Mairinger, S.; Wanek, T.; Mikula, H.*, Cross‐Isotopic Bioorthogonal Tools as Molecular Twins for Radiotheranostic Applications.
ChemBioChem 2019, 20, 1530-1535 (ChemBioTalents issue), doi: 10.1002/cbic.201900042

Levandowski, B. J.^#; Svatunek, D.^#; Sohr, B.; Mikula, H.; Houk, K. N., Secondary Orbital Interactions Enhance the Reactivity of Alkynes in Diels-Alder Cycloadditions.
J. Am. Chem. Soc. 2019, 141, 2224-2227, doi: 10.1021/jacs.8b13088

Svatunek, D.; Houszka, N.; Hamlin, T. A.; Bickelhaupt, F. M.; Mikula, H.*, Chemoselectivity of Tertiary Azides in Strain-Promoted Alkyne-Azide Cycloadditions.
Chem. Eur. J. 2019, 25, 754-758, doi: 10.1002/chem.201805215

Stéen, E. J. L.; Shalgunov, V.; Denk, C.; Mikula, H.; Kjær, A.; Kristensen, J. L.; Herth, M. M., Convenient Entry to ¹⁸F‐Labeled Amines through the Staudinger Reduction.
Eur. J. Org. Chem. 2019, 8, 1722-1725, doi: 10.1002/ejoc.201801457

2018

Skrinjar, P.; Schwarz, M.; Lexmüller, S.; Mechtler, T. P.; Zeyda, M.; Greber-Platzer, S.; Trometer, J.; Kasper, D. C.; Mikula, H.*, Rapid and Modular Assembly of Click Substrates To Assay Enzyme Activity in the Newborn Screening of Lysosomal Storage Disorders.
ACS Cent. Sci. 2018, 4, 1688-1696, doi: 10.1021/acscentsci.8b00668

Miller, M. A.^#; Mikula, H.^#; Luthria, G.; Li, R.; Kronister, S.; Prytyskach, M.; Kohler, R. H., Mitchison, T.; Weissleder, R., Modular Nanoparticulate Prodrug Design Enables Efficient Treatment of Solid Tumors Using Bioorthogonal Activation.
ACS Nano 2018, 12, 12814-12826, doi: 10.1021/acsnano.8b07954

Pineda, J. J,; Miller, M. A.; Song, Y.; Kuhn, H.; Mikula, H.; Tallapragada, N.; Weissleder, R.; Mitchison, T. J., Site occupancy calibration of taxane pharmacology in live cells and tissues.
PNAS 2018, 115, E11406-E11414, doi: 10.1073/pnas.1800047115

Weber, J.; Krauter, S.; Schwarz, T.; Hametner, C.; Mikula, H.*; (2-Benzyloxyphenyl)acetyl (BnPAc): A Participating Relay Protecting Group for Diastereoselective Glycosylation and the Synthesis of 1,2-trans Glycosyl Esters.
Synlett 2018, 29, 2265-2268, doi: 10.1055/s-0037-1610255

Carlson, J. C. T.^#; Mikula, H.^#; Weissleder, R., Unraveling Tetrazine-Triggered Bioorthogonal Elimination Enables Chemical Tools for Ultrafast Release and Universal Cleavage.
J. Am. Chem. Soc. 2018, 140, 3603-3612, doi: 10.1021/jacs.7b11217

Dellafiora, L.; Warth, B.; Schmidt, V.; Del Favero, G.; Mikula, H.; Fröhlich, J.; Marko, D., An integrated in silico/in vitro approach to assess the xenoestrogenic potential of Alternaria mycotoxins and metabolites.
Food Chem. 2018, 248, 253-261, doi: 10.1016/j.foodchem.2017.12.013

Svatunek, D.; Denk, C.; Mikula, H.*, A computational model to predict the Diels–Alder reactivity of aryl/alkyl-substituted tetrazines.
Chemical Monthly (Monatsh. Chem.) 2018, 149, 833-837 (invited), doi: 10.1007/s00706-017-2110-x

Kronister, S.; Svatunek, D.; Denk, C.; Mikula, H.*, Acylation-Mediated ‘Kinetic Turn-On’ of 3-Amino-1,2,4,5-tetrazines.
Synlett 2018, 29, 1297-1302 (Young Investigator Issue; highlighted in SynForm), doi: 10.1055/s-0036-1591764

Puntscher, H.; Kütt, M. L.; Skrinjar, P.; Mikula, H.; Podlech, J.; Marko, D.; Warth, B., Tracking emerging mycotoxins in food: development of an LC-MS/MS method for free and modified Alternaria toxins.
Anal. Bioanal. Chem. 2018, 410, 4481-4494, doi: 10.1007/s00216-018-1105-8

Weber, J.; Schwarz, M.; Schiefer, A.; Hametner, C.; Häubl, G.; Fröhlich, J.; Mikula H.*, Chemical Glucosylation of Labile Natural Products Using a (2-Nitrophenyl)acetyl-Protected Glucosyl Acetimidate Donor.
Eur. J. Org. Chem. 2018, 20-21, 2701-2706, doi: 10.1002/ejoc.201800260

Weber, J.; Vaclavikova, M.; Wiesenberger, G.; Haider, M.; Hametner, C.; Fröhlich, J.; Berthiller, F.; Adam, G.; Mikula, H.; Fruhmann, P., Chemical synthesis of culmorin metabolites and their biologic role in culmorin and acetyl-culmorin treated wheat cells.
Org. Biomol. Chem. 2018, 16, 2043-2048, doi: 10.1039/C7OB02460F

2017

Weber, J.; Fruhmann, P.; Hametner, C.; Schiessl, A.; Häubl, G.; Fröhlich, J.; Mikula, H.*, Synthesis of isotope labeled deoxynivalenol-15-O-glycosides.
Eur. J. Org. Chem. 2017, 47, 7012-7018, doi: 10.1002/ejoc.201700934

Mikula, H.; Stapleton, S.; Kohler, R. H.; Vinegoni, C.; Weissleder, R., Design and Development of Fluorescent Vemurafenib Analogs for In Vivo Imaging.
Theranostics 2017, 7, 1257-1265, doi: 10.7150/thno.18238

Miller, M. A.; Askevold, B.; Mikula, H.; Kohler, R. H.; Pirovich, D.; Weissleder, R.; Nano-palladium is a cellular catalyst for in vivo chemistry.
Nat. Commun. 2017, 8, 15906, doi: 10.1038/ncomms15906

Denk, C.; Wilkovitsch, M.; Skrinjar, P.; Svatunek, D.; Mairinger, S.; Kuntner, C.; Filip, T.; Fröhlich, J.; Wanek, T.; Mikula, H.*, [¹⁸F]Fluoroalkyl azides for rapid radiolabeling and (re)investigation of their potential towards in vivo click chemistry.
Org. Biomol. Chem. 2017, 15, 5976-5982, doi: 10.1039/C7OB00880E

Bintinger, J.; Yang, S.; Fruhmann, P.; Holzer, B.; Stöger, B.; Svirkova, A.; Marchetti-Deschmann, M.; Horkel, E.; Hametner, C.; Fröhlich, J.; Kymissis, I.; Mikula, H., Synthesis, characterization and printing application of alkylated indolo[3,2-b]carbazoles.
Synth. Met. 2017, 228, 9-17, doi: 10.1016/j.synthmet.2017.04.003

Tiessen, C.; Ellmer, D.; Mikula, H.; Pahlke, G.; Warth, B.; Gehrke, H.; Zimmermann, K.; Heiss, E.; Fröhlich, J.; Marko, D., Impact of phase I metabolism on uptake, oxidative stress and genotoxicity of the emerging mycotoxin alternariol and its monomethyl ether in esophageal cells.
Arch. Toxicol. 2017, 91, 1213-1226, doi: 10.1007/s00204-016-1801-0

2014-2016

Meimetis, L. G.; Giedt, R. J.; Mikula, H.; Carlson, J. C.; Kohler, R. H.; Pirovich, D. B.; Weissleder, R., Fluorescent vinblastine probes for live cell imaging.
Chem. Commun. 2016, 52, 9953-9956, doi: 10.1039/c6cc04129a

Denk, C.; Svatunek, D.; Mairinger, S.; Stanek, J.; Filip, T.; Matscheko, D.; Kuntner, C.; Wanek, T.; Mikula, H.*, Design, Synthesis, and Evaluation of a Low-Molecular-Weight ¹¹C-Labeled Tetrazine for Pretargeted PET Imaging Applying Bioorthogonal in Vivo Click Chemistry.
Bioconjugate Chem. 2016, 27, 1707-1712, doi: 10.1021/acs.bioconjchem.6b00234

Svatunek, D.; Denk, C.; Rosecker, V.; Sohr, B.; Hametner, C.; Allmaier, G.; Froehlich, J.; Mikula, H.*, Efficient low-cost preparation of trans-cyclooctenes using a simplified flow setup for photoisomerization.
Monatsh. Chem. (Chemical Monthly) 2016, 147, 579-585 (invited), doi: 10.1007/s00706-016-1668-z

Walravens, J.; Mikula, H.; Rychlik, M.; Asam, S.; Devos, T.; Njumbe Ediage, E.; Diana Di Mavungu, J.; Jacxsens, L.; Van Landschoot, A.; Vanhaecke, L.; De Saeger, S., Validated UPLC-MS/MS Methods To Quantitate Free and Conjugated Alternaria Toxins in Commercially Available Tomato Products and Fruit and Vegetable Juices in Belgium.
J. Agric. Food Chem. 2016, 64, 5101-5109, doi: 10.1021/acs.jafc.6b01029

Kim, E.; Yang, K. S.; Kohler, R. H.; Dubach, J. M.; Mikula, H.; Weissleder, R., Optimized Near-IR Fluorescent Agents for in Vivo Imaging of Btk Expression.
Bioconjugate Chem. 2015, 26, 1513-1518, doi: 10.1021/acs.bioconjchem.5b00152

Denk, C.; Svatunek, D.; Filip, T.; Wanek, T.; Lumpi, D.; Froehlich, J.; Kuntner, C.; Mikula, H.*, Development of a 18F-Labeled Tetrazine with Favorable Pharmacokinetics for Bioorthogonal PET Imaging.
Angew. Chem. Int. Ed. 2014, 53, 9655-9659, doi: 10.1002/anie.201404277

Walravens, J.; Mikula, H.; Rychlik, M.; Asam, S.; Ediage, E. N.; Di Mavungu, J. D.; Van Landschoot, A.; Vanhaecke, L.; De Saeger, S., Development and validation of an ultra-high-performance liquid chromatography tandem mass spectrometric method for the simultaneous determination of free and conjugated Alternaria toxins in cereal-based foodstuffs.
J. Chromatogr. A 2014, 1372, 91-101, doi: 10.1016/j.chroma.2014.10.083

Fruhmann, P.; Skrinjar, P.; Weber, J.; Mikula, H.; Warth, B.; Sulyok, M.; Krska, R.; Adam, G.; Rosenberg, E.; Hametner, C.; Froehlich, J., Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin. 
Tetrahedron 2014, 70, 5260-5266, doi: 10.1016/j.tet.2014.05.064

Fruhmann, P.; Weigl-Pollack, T.; Mikula, H.*; Wiesenberger, G.; Adam, G.; Varga, E.; Berthiller, F.; Krska, R.; Hametner, C.; Froehlich, J., Methylthiodeoxynivalenol (MTD): Insight into the chemistry, structure and toxicity of thia-Michael adducts of trichothecenes. 
Org. Biomol. Chem. 2014, 12, 5144-5150, doi: 10.1039/C4OB00458B

Mikula, H.*; Weber, J.; Svatunek, D.; Skrinjar, P.; Adam, G.; Krska, R.; Hametner, C.; Froehlich, J., Synthesis of zearalenone-16-beta,D-glucoside and zearalenone-16-sulfate: A tale of protecting resorcylic acid lactones for regiocontrolled conjugation.
Beilstein J. Org. Chem. 2014, 10, 1129-1134, doi: 10.3762/bjoc.10.112

Mikula, H.*; Svatunek, D.; Skrinjar, P.; Horkel, E.; Hametner, C.; Froehlich, J., DFT study of the Lewis acid mediated synthesis of 3-acyltetramic acids.
J. Mol. Model. 2014, 20, 2181, doi: 10.1007/s00894-014-2181-0

Fruhmann, P.^#; Mikula, H.^#; Wiesenberger, G.; Varga, E.; Lumpi, D.; Stoeger, B.; Haeubl, G.; Lemmens, M.; Berthiller, F.; Krska, R.; Adam, G.; Hametner, C.; Froehlich, J., Isolation and Structure Elucidation of Pentahydroxyscirpene, a Trichothecene Fusarium Mycotoxin.
J. Nat. Prod. 2014, 77, 188-192, doi: 10.1021/np4008365

Fruhmann, P.; Hametner, C.; Mikula, H.; Adam, G.; Krska, R.; Froehlich, J., Stereoselective Luche Reduction of Deoxynivalenol and Three of Its Acetylated Derivatives at C8.
Toxins 2014, 6, 325-336, doi: 10.3390/toxins6010325

before 2014

Mikula, H.*; Skrinjar, P.; Sohr, B.; Ellmer, D.; Hametner, C.; Froehlich, J., Total synthesis of masked Alternaria mycotoxins-sulfates and glucosides of alternariol (AOH) and alternariol-9-methyl ether (AME).
Tetrahedron 2013, 69, 10322-10330, doi: 10.1016/j.tet.2013.10.008

Weber, J.; Mikula, H.*; Fruhmann, P.; Hametner, C.; Varga, E.; Berthiller, F.; Krska, R.; Froehlich, J., Gentiobiosylation of beta-Resorcylic Acid Esters and Lactones: First Synthesis and Characterization of Zearalenone-14-beta,D-Gentiobioside.
Synlett 2013, 24, 1830-1834, doi: 10.1055/s-0033-1339338

Mikula, H.*; Hametner, C.; Froehlich, J., Zearalenone Mimics: Synthesis Of (E)-6-(1-Alkenyl)-Substituted beta-Resorcylic Acid Esters.
Synth. Commun. 2013, 43, 1939-1946, doi: 10.1080/00397911.2012.681827

Mikula, H.*; Sohr, B.; Skrinjar, P.; Weber, J.; Hametner, C.; Berthiller, F.; Krska, R.; Adam, G.; Fröhlich, J., Sulfation of beta-resorcylic acid esters-first synthesis of zearalenone-14-sulfate.
Tetrahedron Lett. 2013, 54, 3290-3293, doi: 10.1016/j.tetlet.2013.04.059

Mikula, H.*; Weber, J.; Lexmueller, S.; Bichl, G.; Schwartz, H.; Varga, E.; Berthiller, F.; Hametner, C.; Krska, R.; Froehlich, J., Simultaneous preparation of alpha/beta-zearalenol glucosides and glucuronides.
Carbohydr. Res. 2013, 373, 59-63, doi: 10.1016/j.carres.2013.03.002

Mikula, H.*; Horkel, E.; Hans, P.; Hametner, C.; Froehlich, J., Structure and tautomerism of tenuazonic acid - A synergetic computational and spectroscopic approach.
J. Hazard. Mat. 2013, 250, 308-317, doi: 10.1016/j.jhazmat.2013.02.006

Mikula, H.*; Matscheko, D.; Schwarz, M.; Hametner, C.; Froehlich, J., Improved and large-scale synthesis of different protected D-glucuronals.
Carbohydr. Res. 2013, 370, 19-23, doi: 10.1016/j.carres.2013.01.007

Mikula, H.*; Svatunek, D.; Lumpi, D.; Gloecklhofer, F.; Hametner, C.; Froehlich, J., Practical and Efficient Large-Scale Preparation of Dimethyldioxirane.
Org. Proc. Res. Dev. 2013, 17, 313-316, doi: 10.1021/op300338q

Mikula, H.*; Hametner, C.; Berthiller, F.; Warth, B.; Krska, R.; Adam, G.; Fröhlich, J., Fast and reproducible chemical synthesis of zearalenone-14-β,D- glucuronide. 
World Mycotoxin J. 2012, 5, 289-296, doi: 10.3920/WMJ2012.1404

Warth, B.; Sulyok, M.; Fruhmann, P.; Mikula, H.; Berthiller, F.; Schuhmacher, R.; Hametner, C.; Abia, W. A.; Adam, G.; Fröhlich, J.; Krska, A., Development and validation of a rapid multi-biomarker liquid chromatography/tandem mass spectrometry method to assess human exposure to mycotoxins. 
Rapid Commun. Mass Spectrom. 2012, 26, 1533-1540, doi: 10.1002/rcm.6255

Pfeiffer, E.; Hildebrand, A.; Mikula, H.; Metzler, M., Glucuronidation of Zearalenone, zeranol, and four metabolites in vitro: formation of glucuronides by various microsomes and humad UDP-glucuronosyltransferase isoforms. 
Mol. Nutr. Food Res. 2010, 54, 1468-1476, doi: 10.1002/mnfr.200900524