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X-ray Spectroscopic Verification of the Active Species in Iron-Catalyzed Cross-Coupling Reactions. <i>Chemistry - A European Journal</i>. 2013;19(47):15816-15821. doi:<a href=\"https://doi.org/10.1002/chem.201303340\">10.1002/chem.201303340</a>","short":"R. Schoch, W. Desens, T. Werner, M. Bauer, Chemistry - A European Journal 19 (2013) 15816–15821.","chicago":"Schoch, Roland, Willi Desens, Thomas Werner, and Matthias Bauer. “X-Ray Spectroscopic Verification of the Active Species in Iron-Catalyzed Cross-Coupling Reactions.” <i>Chemistry - A European Journal</i> 19, no. 47 (2013): 15816–21. <a href=\"https://doi.org/10.1002/chem.201303340\">https://doi.org/10.1002/chem.201303340</a>.","ieee":"R. Schoch, W. Desens, T. Werner, and M. Bauer, “X-ray Spectroscopic Verification of the Active Species in Iron-Catalyzed Cross-Coupling Reactions,” <i>Chemistry - A European Journal</i>, vol. 19, no. 47, pp. 15816–15821, 2013, doi: <a href=\"https://doi.org/10.1002/chem.201303340\">10.1002/chem.201303340</a>.","mla":"Schoch, Roland, et al. “X-Ray Spectroscopic Verification of the Active Species in Iron-Catalyzed Cross-Coupling Reactions.” <i>Chemistry - A European Journal</i>, vol. 19, no. 47, Wiley, 2013, pp. 15816–21, doi:<a href=\"https://doi.org/10.1002/chem.201303340\">10.1002/chem.201303340</a>.","apa":"Schoch, R., Desens, W., Werner, T., &#38; Bauer, M. (2013). X-ray Spectroscopic Verification of the Active Species in Iron-Catalyzed Cross-Coupling Reactions. <i>Chemistry - A European Journal</i>, <i>19</i>(47), 15816–15821. <a href=\"https://doi.org/10.1002/chem.201303340\">https://doi.org/10.1002/chem.201303340</a>"}},{"author":[{"full_name":"Elsässer, Brigitta","last_name":"Elsässer","first_name":"Brigitta"},{"id":"16203","first_name":"Silvia","last_name":"Dohmeier-Fischer","full_name":"Dohmeier-Fischer, Silvia"},{"last_name":"Fels","first_name":"Gregor","full_name":"Fels, Gregor"}],"publication_identifier":{"issn":["1610-2940","0948-5023"]},"year":"2012","title":"Theoretical investigation of the enzymatic phosphoryl transfer of β-phosphoglucomutase: revisiting both steps of the catalytic cycle","status":"public","publication_status":"published","date_updated":"2022-01-06T06:52:46Z","_id":"16242","language":[{"iso":"eng"}],"page":"3169-3179","user_id":"16203","doi":"10.1007/s00894-011-1344-5","citation":{"chicago":"Elsässer, Brigitta, Silvia Dohmeier-Fischer, and Gregor Fels. “Theoretical Investigation of the Enzymatic Phosphoryl Transfer of β-Phosphoglucomutase: Revisiting Both Steps of the Catalytic Cycle.” <i>Journal of Molecular Modeling</i>, 2012, 3169–79. <a href=\"https://doi.org/10.1007/s00894-011-1344-5\">https://doi.org/10.1007/s00894-011-1344-5</a>.","short":"B. Elsässer, S. Dohmeier-Fischer, G. Fels, Journal of Molecular Modeling (2012) 3169–3179.","ama":"Elsässer B, Dohmeier-Fischer S, Fels G. Theoretical investigation of the enzymatic phosphoryl transfer of β-phosphoglucomutase: revisiting both steps of the catalytic cycle. <i>Journal of Molecular Modeling</i>. 2012:3169-3179. doi:<a href=\"https://doi.org/10.1007/s00894-011-1344-5\">10.1007/s00894-011-1344-5</a>","bibtex":"@article{Elsässer_Dohmeier-Fischer_Fels_2012, title={Theoretical investigation of the enzymatic phosphoryl transfer of β-phosphoglucomutase: revisiting both steps of the catalytic cycle}, DOI={<a href=\"https://doi.org/10.1007/s00894-011-1344-5\">10.1007/s00894-011-1344-5</a>}, journal={Journal of Molecular Modeling}, author={Elsässer, Brigitta and Dohmeier-Fischer, Silvia and Fels, Gregor}, year={2012}, pages={3169–3179} }","apa":"Elsässer, B., Dohmeier-Fischer, S., &#38; Fels, G. (2012). Theoretical investigation of the enzymatic phosphoryl transfer of β-phosphoglucomutase: revisiting both steps of the catalytic cycle. <i>Journal of Molecular Modeling</i>, 3169–3179. <a href=\"https://doi.org/10.1007/s00894-011-1344-5\">https://doi.org/10.1007/s00894-011-1344-5</a>","mla":"Elsässer, Brigitta, et al. “Theoretical Investigation of the Enzymatic Phosphoryl Transfer of β-Phosphoglucomutase: Revisiting Both Steps of the Catalytic Cycle.” <i>Journal of Molecular Modeling</i>, 2012, pp. 3169–79, doi:<a href=\"https://doi.org/10.1007/s00894-011-1344-5\">10.1007/s00894-011-1344-5</a>.","ieee":"B. Elsässer, S. Dohmeier-Fischer, and G. Fels, “Theoretical investigation of the enzymatic phosphoryl transfer of β-phosphoglucomutase: revisiting both steps of the catalytic cycle,” <i>Journal of Molecular Modeling</i>, pp. 3169–3179, 2012."},"publication":"Journal of Molecular Modeling","date_created":"2020-03-04T10:02:52Z","department":[{"_id":"35"},{"_id":"390"}],"type":"journal_article"},{"citation":{"mla":"Greb, Lutz, and Jan Paradies. “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry.” <i>Topics in Current Chemistry</i>, Springer Berlin Heidelberg, 2012, doi:<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>.","ama":"Greb L, Paradies J. Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry. In: <i>Topics in Current Chemistry</i>. Springer Berlin Heidelberg; 2012. doi:<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>","bibtex":"@inbook{Greb_Paradies_2012, place={Berlin, Heidelberg}, title={Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry}, DOI={<a href=\"https://doi.org/10.1007/128_2012_375\">10.1007/128_2012_375</a>}, booktitle={Topics in Current Chemistry}, publisher={Springer Berlin Heidelberg}, author={Greb, Lutz and Paradies, Jan}, year={2012} }","apa":"Greb, L., &#38; Paradies, J. (2012). Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry. In <i>Topics in Current Chemistry</i>. Springer Berlin Heidelberg. <a href=\"https://doi.org/10.1007/128_2012_375\">https://doi.org/10.1007/128_2012_375</a>","ieee":"L. Greb and J. Paradies, “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry,” in <i>Topics in Current Chemistry</i>, Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.","short":"L. Greb, J. Paradies, in: Topics in Current Chemistry, Springer Berlin Heidelberg, Berlin, Heidelberg, 2012.","chicago":"Greb, Lutz, and Jan Paradies. “Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry.” In <i>Topics in Current Chemistry</i>. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. <a href=\"https://doi.org/10.1007/128_2012_375\">https://doi.org/10.1007/128_2012_375</a>."},"publication":"Topics in Current Chemistry","department":[{"_id":"2"},{"_id":"389"}],"type":"book_chapter","date_created":"2026-03-11T10:32:32Z","place":"Berlin, Heidelberg","publication_status":"published","date_updated":"2026-03-11T10:32:41Z","author":[{"full_name":"Greb, Lutz","first_name":"Lutz","last_name":"Greb"},{"id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"publication_identifier":{"issn":["0340-1022","1436-5049"],"isbn":["9783642377587","9783642377594"]},"title":"Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry","year":"2012","status":"public","user_id":"53339","doi":"10.1007/128_2012_375","publisher":"Springer Berlin Heidelberg","_id":"64901","language":[{"iso":"eng"}]},{"department":[{"_id":"163"}],"keyword":["General Chemistry"],"type":"journal_article","date_created":"2022-06-28T12:28:49Z","abstract":[{"text":"<jats:p>A rapid and convenient preparation of acyclic imides by the reaction of\r\n   aliphatic and aromatic nitriles with acyclic carboxylic anhydride in the\r\n   presence of catalytic amounts of p-toluenesulfonic acid under thermal or\r\n   ultrasonic conditions is reported. The advantages of this procedure are\r\n   moderate reaction times, good to excellent yields, use of inexpensive and\r\n   ecofriendly catalyst. The reaction of nitriles with aliphatic anhydrides\r\n   proceeds in thermal conditions, while by the use of ultrasound irradiations\r\n   these reactions get accelerated.</jats:p>","lang":"eng"}],"extern":"1","publication":"Journal of the Serbian Chemical Society","issue":"4","doi":"10.2298/jsc110511168n","language":[{"iso":"eng"}],"intvolume":"        77","date_updated":"2022-06-28T12:34:17Z","publication_status":"published","author":[{"full_name":"Nasr-Esfahani, Masoud","last_name":"Nasr-Esfahani","first_name":"Masoud"},{"full_name":"Montazerozohori, Morteza","first_name":"Morteza","last_name":"Montazerozohori"},{"id":"77435","first_name":"Najmeh","last_name":"Filvan Torkaman","full_name":"Filvan Torkaman, Najmeh"}],"publication_identifier":{"issn":["0352-5139","1820-7421"]},"year":"2011","title":"Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions","citation":{"short":"M. Nasr-Esfahani, M. Montazerozohori, N. Filvan Torkaman, Journal of the Serbian Chemical Society 77 (2011) 415–421.","chicago":"Nasr-Esfahani, Masoud, Morteza Montazerozohori, and Najmeh Filvan Torkaman. “Ultrasound-Assisted Catalytic Synthesis of Acyclic Imides in the Presence of p-Toluenesulfonic Acid under Solvent Free Conditions.” <i>Journal of the Serbian Chemical Society</i> 77, no. 4 (2011): 415–21. <a href=\"https://doi.org/10.2298/jsc110511168n\">https://doi.org/10.2298/jsc110511168n</a>.","apa":"Nasr-Esfahani, M., Montazerozohori, M., &#38; Filvan Torkaman, N. (2011). Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions. <i>Journal of the Serbian Chemical Society</i>, <i>77</i>(4), 415–421. <a href=\"https://doi.org/10.2298/jsc110511168n\">https://doi.org/10.2298/jsc110511168n</a>","ieee":"M. Nasr-Esfahani, M. Montazerozohori, and N. Filvan Torkaman, “Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions,” <i>Journal of the Serbian Chemical Society</i>, vol. 77, no. 4, pp. 415–421, 2011, doi: <a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>.","ama":"Nasr-Esfahani M, Montazerozohori M, Filvan Torkaman N. Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions. <i>Journal of the Serbian Chemical Society</i>. 2011;77(4):415-421. doi:<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>","bibtex":"@article{Nasr-Esfahani_Montazerozohori_Filvan Torkaman_2011, title={Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions}, volume={77}, DOI={<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>}, number={4}, journal={Journal of the Serbian Chemical Society}, publisher={National Library of Serbia}, author={Nasr-Esfahani, Masoud and Montazerozohori, Morteza and Filvan Torkaman, Najmeh}, year={2011}, pages={415–421} }","mla":"Nasr-Esfahani, Masoud, et al. “Ultrasound-Assisted Catalytic Synthesis of Acyclic Imides in the Presence of p-Toluenesulfonic Acid under Solvent Free Conditions.” <i>Journal of the Serbian Chemical Society</i>, vol. 77, no. 4, National Library of Serbia, 2011, pp. 415–21, doi:<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>."},"volume":77,"user_id":"77435","_id":"32265","publisher":"National Library of Serbia","page":"415-421","status":"public"},{"publisher":"Georg Thieme Verlag KG","_id":"38007","page":"3482-3490","volume":2011,"user_id":"89271","status":"public","citation":{"bibtex":"@article{Werner_Riahi_Schramm_2011, title={Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes}, volume={2011}, DOI={<a href=\"https://doi.org/10.1055/s-0030-1260230\">10.1055/s-0030-1260230</a>}, number={21}, journal={Synthesis}, publisher={Georg Thieme Verlag KG}, author={Werner, Thomas and Riahi, Abdol and Schramm, Heiko}, year={2011}, pages={3482–3490} }","ama":"Werner T, Riahi A, Schramm H. Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes. <i>Synthesis</i>. 2011;2011(21):3482-3490. doi:<a href=\"https://doi.org/10.1055/s-0030-1260230\">10.1055/s-0030-1260230</a>","mla":"Werner, Thomas, et al. “Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes.” <i>Synthesis</i>, vol. 2011, no. 21, Georg Thieme Verlag KG, 2011, pp. 3482–90, doi:<a href=\"https://doi.org/10.1055/s-0030-1260230\">10.1055/s-0030-1260230</a>.","short":"T. Werner, A. Riahi, H. Schramm, Synthesis 2011 (2011) 3482–3490.","chicago":"Werner, Thomas, Abdol Riahi, and Heiko Schramm. “Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes.” <i>Synthesis</i> 2011, no. 21 (2011): 3482–90. <a href=\"https://doi.org/10.1055/s-0030-1260230\">https://doi.org/10.1055/s-0030-1260230</a>.","ieee":"T. Werner, A. Riahi, and H. Schramm, “Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes,” <i>Synthesis</i>, vol. 2011, no. 21, pp. 3482–3490, 2011, doi: <a href=\"https://doi.org/10.1055/s-0030-1260230\">10.1055/s-0030-1260230</a>.","apa":"Werner, T., Riahi, A., &#38; Schramm, H. (2011). Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes. <i>Synthesis</i>, <i>2011</i>(21), 3482–3490. <a href=\"https://doi.org/10.1055/s-0030-1260230\">https://doi.org/10.1055/s-0030-1260230</a>"},"language":[{"iso":"eng"}],"doi":"10.1055/s-0030-1260230","publication_identifier":{"issn":["0039-7881","1437-210X"]},"author":[{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"},{"last_name":"Riahi","first_name":"Abdol","full_name":"Riahi, Abdol"},{"full_name":"Schramm, Heiko","first_name":"Heiko","last_name":"Schramm"}],"year":"2011","title":"Phosphonium Salt Catalyzed Addition of Diethylzinc to Aldehydes","intvolume":"      2011","date_updated":"2025-11-10T09:40:42Z","publication_status":"published","date_created":"2023-01-22T21:11:42Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2"],"issue":"21","publication":"Synthesis","extern":"1"},{"status":"public","user_id":"89271","volume":2010,"page":"6904-6907","_id":"38008","publisher":"Wiley","citation":{"ama":"Werner T, Koch J. Sodium Hydride Catalyzed Tishchenko Reaction. <i>European Journal of Organic Chemistry</i>. 2010;2010(36):6904-6907. doi:<a href=\"https://doi.org/10.1002/ejoc.201001294\">10.1002/ejoc.201001294</a>","bibtex":"@article{Werner_Koch_2010, title={Sodium Hydride Catalyzed Tishchenko Reaction}, volume={2010}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201001294\">10.1002/ejoc.201001294</a>}, number={36}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Werner, Thomas and Koch, Juliane}, year={2010}, pages={6904–6907} }","mla":"Werner, Thomas, and Juliane Koch. “Sodium Hydride Catalyzed Tishchenko Reaction.” <i>European Journal of Organic Chemistry</i>, vol. 2010, no. 36, Wiley, 2010, pp. 6904–07, doi:<a href=\"https://doi.org/10.1002/ejoc.201001294\">10.1002/ejoc.201001294</a>.","chicago":"Werner, Thomas, and Juliane Koch. “Sodium Hydride Catalyzed Tishchenko Reaction.” <i>European Journal of Organic Chemistry</i> 2010, no. 36 (2010): 6904–7. <a href=\"https://doi.org/10.1002/ejoc.201001294\">https://doi.org/10.1002/ejoc.201001294</a>.","short":"T. Werner, J. Koch, European Journal of Organic Chemistry 2010 (2010) 6904–6907.","apa":"Werner, T., &#38; Koch, J. (2010). Sodium Hydride Catalyzed Tishchenko Reaction. <i>European Journal of Organic Chemistry</i>, <i>2010</i>(36), 6904–6907. <a href=\"https://doi.org/10.1002/ejoc.201001294\">https://doi.org/10.1002/ejoc.201001294</a>","ieee":"T. Werner and J. Koch, “Sodium Hydride Catalyzed Tishchenko Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2010, no. 36, pp. 6904–6907, 2010, doi: <a href=\"https://doi.org/10.1002/ejoc.201001294\">10.1002/ejoc.201001294</a>."},"publication_status":"published","date_updated":"2025-11-10T09:41:27Z","intvolume":"      2010","title":"Sodium Hydride Catalyzed Tishchenko Reaction","year":"2010","publication_identifier":{"issn":["1434-193X"]},"author":[{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"},{"full_name":"Koch, Juliane","first_name":"Juliane","last_name":"Koch"}],"doi":"10.1002/ejoc.201001294","language":[{"iso":"eng"}],"extern":"1","publication":"European Journal of Organic Chemistry","issue":"36","keyword":["T3"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:12:03Z"},{"citation":{"ieee":"T. Werner, “Phosphonium Salt Organocatalysis,” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 351, no. 10, pp. 1469–1481, 2009, doi: <a href=\"https://doi.org/10.1002/adsc.200900211\">10.1002/adsc.200900211</a>.","apa":"Werner, T. (2009). Phosphonium Salt Organocatalysis. <i>Advanced Synthesis &#38;amp; Catalysis</i>, <i>351</i>(10), 1469–1481. <a href=\"https://doi.org/10.1002/adsc.200900211\">https://doi.org/10.1002/adsc.200900211</a>","short":"T. Werner, Advanced Synthesis &#38;amp; Catalysis 351 (2009) 1469–1481.","chicago":"Werner, Thomas. “Phosphonium Salt Organocatalysis.” <i>Advanced Synthesis &#38;amp; Catalysis</i> 351, no. 10 (2009): 1469–81. <a href=\"https://doi.org/10.1002/adsc.200900211\">https://doi.org/10.1002/adsc.200900211</a>.","mla":"Werner, Thomas. “Phosphonium Salt Organocatalysis.” <i>Advanced Synthesis &#38;amp; Catalysis</i>, vol. 351, no. 10, Wiley, 2009, pp. 1469–81, doi:<a href=\"https://doi.org/10.1002/adsc.200900211\">10.1002/adsc.200900211</a>.","bibtex":"@article{Werner_2009, title={Phosphonium Salt Organocatalysis}, volume={351}, DOI={<a href=\"https://doi.org/10.1002/adsc.200900211\">10.1002/adsc.200900211</a>}, number={10}, journal={Advanced Synthesis &#38;amp; Catalysis}, publisher={Wiley}, author={Werner, Thomas}, year={2009}, pages={1469–1481} }","ama":"Werner T. Phosphonium Salt Organocatalysis. <i>Advanced Synthesis &#38;amp; Catalysis</i>. 2009;351(10):1469-1481. doi:<a href=\"https://doi.org/10.1002/adsc.200900211\">10.1002/adsc.200900211</a>"},"publisher":"Wiley","_id":"38009","page":"1469-1481","volume":351,"user_id":"89271","status":"public","date_created":"2023-01-22T21:12:23Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2"],"type":"journal_article","issue":"10","publication":"Advanced Synthesis &amp; Catalysis","extern":"1","language":[{"iso":"eng"}],"doi":"10.1002/adsc.200900211","publication_identifier":{"issn":["1615-4150","1615-4169"]},"author":[{"id":"89271","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas"}],"title":"Phosphonium Salt Organocatalysis","year":"2009","intvolume":"       351","publication_status":"published","date_updated":"2025-11-10T09:41:55Z"},{"language":[{"iso":"eng"}],"doi":"10.1021/ja803445u","year":"2008","title":"Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β","publication_identifier":{"issn":["0002-7863","1520-5126"]},"author":[{"full_name":"Navarro, Ismael","first_name":"Ismael","last_name":"Navarro"},{"full_name":"Basset, Jean-François","first_name":"Jean-François","last_name":"Basset"},{"full_name":"Hebbe, Séverine","first_name":"Séverine","last_name":"Hebbe"},{"full_name":"Major, Sarah M.","last_name":"Major","first_name":"Sarah M."},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"last_name":"Howsham","first_name":"Catherine","full_name":"Howsham, Catherine"},{"first_name":"Jan","last_name":"Bräckow","full_name":"Bräckow, Jan"},{"full_name":"Barrett, Anthony G. M.","last_name":"Barrett","first_name":"Anthony G. M."}],"date_updated":"2026-02-24T14:31:00Z","publication_status":"published","intvolume":"       130","date_created":"2023-01-22T21:12:47Z","keyword":["Colloid and Surface Chemistry","Biochemistry","General Chemistry","Catalysis"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"issue":"31","publication":"Journal of the American Chemical Society","extern":"1","page":"10293-10298","_id":"38010","publisher":"American Chemical Society (ACS)","user_id":"14972","volume":130,"status":"public","citation":{"mla":"Navarro, Ismael, et al. “Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β.” <i>Journal of the American Chemical Society</i>, vol. 130, no. 31, American Chemical Society (ACS), 2008, pp. 10293–98, doi:<a href=\"https://doi.org/10.1021/ja803445u\">10.1021/ja803445u</a>.","bibtex":"@article{Navarro_Basset_Hebbe_Major_Werner_Howsham_Bräckow_Barrett_2008, title={Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β}, volume={130}, DOI={<a href=\"https://doi.org/10.1021/ja803445u\">10.1021/ja803445u</a>}, number={31}, journal={Journal of the American Chemical Society}, publisher={American Chemical Society (ACS)}, author={Navarro, Ismael and Basset, Jean-François and Hebbe, Séverine and Major, Sarah M. and Werner, Thomas and Howsham, Catherine and Bräckow, Jan and Barrett, Anthony G. M.}, year={2008}, pages={10293–10298} }","ama":"Navarro I, Basset J-F, Hebbe S, et al. Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β. <i>Journal of the American Chemical Society</i>. 2008;130(31):10293-10298. doi:<a href=\"https://doi.org/10.1021/ja803445u\">10.1021/ja803445u</a>","ieee":"I. Navarro <i>et al.</i>, “Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β,” <i>Journal of the American Chemical Society</i>, vol. 130, no. 31, pp. 10293–10298, 2008, doi: <a href=\"https://doi.org/10.1021/ja803445u\">10.1021/ja803445u</a>.","apa":"Navarro, I., Basset, J.-F., Hebbe, S., Major, S. M., Werner, T., Howsham, C., Bräckow, J., &#38; Barrett, A. G. M. (2008). Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β. <i>Journal of the American Chemical Society</i>, <i>130</i>(31), 10293–10298. <a href=\"https://doi.org/10.1021/ja803445u\">https://doi.org/10.1021/ja803445u</a>","chicago":"Navarro, Ismael, Jean-François Basset, Séverine Hebbe, Sarah M. Major, Thomas Werner, Catherine Howsham, Jan Bräckow, and Anthony G. M. Barrett. “Biomimetic Synthesis of Resorcylate Natural Products Utilizing Late Stage Aromatization: Concise Total Syntheses of the Marine Antifungal Agents 15G256ι and 15G256β.” <i>Journal of the American Chemical Society</i> 130, no. 31 (2008): 10293–98. <a href=\"https://doi.org/10.1021/ja803445u\">https://doi.org/10.1021/ja803445u</a>.","short":"I. Navarro, J.-F. Basset, S. Hebbe, S.M. Major, T. Werner, C. Howsham, J. Bräckow, A.G.M. Barrett, Journal of the American Chemical Society 130 (2008) 10293–10298."}},{"user_id":"23547","_id":"25987","page":"335-341","status":"public","quality_controlled":"1","citation":{"bibtex":"@article{Roggenbuck_Schäfer_Tsoncheva_Minchev_Hanss_Tiemann_2007, title={Mesoporous CeO2: Synthesis by nanocasting, characterisation and catalytic properties}, DOI={<a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">10.1016/j.micromeso.2006.11.029</a>}, journal={Microporous and Mesoporous Materials}, author={Roggenbuck, Jan and Schäfer, Hanno and Tsoncheva, Tanya and Minchev, Christo and Hanss, Jan and Tiemann, Michael}, year={2007}, pages={335–341} }","ama":"Roggenbuck J, Schäfer H, Tsoncheva T, Minchev C, Hanss J, Tiemann M. Mesoporous CeO2: Synthesis by nanocasting, characterisation and catalytic properties. <i>Microporous and Mesoporous Materials</i>. Published online 2007:335-341. doi:<a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">10.1016/j.micromeso.2006.11.029</a>","mla":"Roggenbuck, Jan, et al. “Mesoporous CeO2: Synthesis by Nanocasting, Characterisation and Catalytic Properties.” <i>Microporous and Mesoporous Materials</i>, 2007, pp. 335–41, doi:<a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">10.1016/j.micromeso.2006.11.029</a>.","short":"J. Roggenbuck, H. Schäfer, T. Tsoncheva, C. Minchev, J. Hanss, M. Tiemann, Microporous and Mesoporous Materials (2007) 335–341.","chicago":"Roggenbuck, Jan, Hanno Schäfer, Tanya Tsoncheva, Christo Minchev, Jan Hanss, and Michael Tiemann. “Mesoporous CeO2: Synthesis by Nanocasting, Characterisation and Catalytic Properties.” <i>Microporous and Mesoporous Materials</i>, 2007, 335–41. <a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">https://doi.org/10.1016/j.micromeso.2006.11.029</a>.","ieee":"J. Roggenbuck, H. Schäfer, T. Tsoncheva, C. Minchev, J. Hanss, and M. Tiemann, “Mesoporous CeO2: Synthesis by nanocasting, characterisation and catalytic properties,” <i>Microporous and Mesoporous Materials</i>, pp. 335–341, 2007, doi: <a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">10.1016/j.micromeso.2006.11.029</a>.","apa":"Roggenbuck, J., Schäfer, H., Tsoncheva, T., Minchev, C., Hanss, J., &#38; Tiemann, M. (2007). Mesoporous CeO2: Synthesis by nanocasting, characterisation and catalytic properties. <i>Microporous and Mesoporous Materials</i>, 335–341. <a href=\"https://doi.org/10.1016/j.micromeso.2006.11.029\">https://doi.org/10.1016/j.micromeso.2006.11.029</a>"},"doi":"10.1016/j.micromeso.2006.11.029","language":[{"iso":"eng"}],"article_type":"original","date_updated":"2023-03-09T08:48:18Z","publication_status":"published","author":[{"full_name":"Roggenbuck, Jan","first_name":"Jan","last_name":"Roggenbuck"},{"first_name":"Hanno","last_name":"Schäfer","full_name":"Schäfer, Hanno"},{"full_name":"Tsoncheva, Tanya","first_name":"Tanya","last_name":"Tsoncheva"},{"last_name":"Minchev","first_name":"Christo","full_name":"Minchev, Christo"},{"last_name":"Hanss","first_name":"Jan","full_name":"Hanss, Jan"},{"first_name":"Michael","last_name":"Tiemann","orcid":"0000-0003-1711-2722","full_name":"Tiemann, Michael","id":"23547"}],"publication_identifier":{"issn":["1387-1811"]},"title":"Mesoporous CeO2: Synthesis by nanocasting, characterisation and catalytic properties","year":"2007","department":[{"_id":"35"},{"_id":"163"},{"_id":"307"}],"type":"journal_article","date_created":"2021-10-09T09:41:24Z","abstract":[{"text":"Mesoporous CeO2 was synthesised by using CMK-3 carbon as a structure matrix. Nitrogen physisorption, powder X-ray diffraction, transmission electron microscopy (TEM), selected-area electron diffraction (SAED), energy-dispersive X-ray (EDX), X-ray absorption near-edge structure (XANES), and thermal (TG/MS) analysis were used for their characterisation. Methanol decomposition to hydrogen, CO, and methane was used as a catalytic test reaction. The obtained products exhibit uniform pores with a diameter of ca. 5 nm in a two-dimensional hexagonal periodic arrangement, as well as interparticle porosity, broadly distributed around ca. 35 nm; the specific surface area is 148 m2 g−1. The pore walls are polycrystalline. The polycrystalline nature and high surface-to-volume ratio of the products is reflected in an increased signal intensity in X-ray absorption spectroscopy. The synthesis of CeO2 from Ce(NO3)3 within the pores of the carbon matrix and the subsequent thermal combustion of the carbon is monitored by thermal analysis. Catalytic tests reveal that the activity of the mesoporous products in methanol decomposition are substantially higher than for a non-porous sample.","lang":"eng"}],"extern":"1","publication":"Microporous and Mesoporous Materials"},{"citation":{"chicago":"Christoffers, Jens, Thomas Werner, and Michael Rössle. “Cerium-Catalyzed Oxidative C–C Bond Forming Reactions.” <i>Catalysis Today</i> 121, no. 1–2 (2007): 22–26. <a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">https://doi.org/10.1016/j.cattod.2006.11.008</a>.","ama":"Christoffers J, Werner T, Rössle M. Cerium-catalyzed oxidative C–C bond forming reactions. <i>Catalysis Today</i>. 2007;121(1-2):22-26. doi:<a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">10.1016/j.cattod.2006.11.008</a>","short":"J. Christoffers, T. Werner, M. Rössle, Catalysis Today 121 (2007) 22–26.","bibtex":"@article{Christoffers_Werner_Rössle_2007, title={Cerium-catalyzed oxidative C–C bond forming reactions}, volume={121}, DOI={<a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">10.1016/j.cattod.2006.11.008</a>}, number={1–2}, journal={Catalysis Today}, publisher={Elsevier BV}, author={Christoffers, Jens and Werner, Thomas and Rössle, Michael}, year={2007}, pages={22–26} }","mla":"Christoffers, Jens, et al. “Cerium-Catalyzed Oxidative C–C Bond Forming Reactions.” <i>Catalysis Today</i>, vol. 121, no. 1–2, Elsevier BV, 2007, pp. 22–26, doi:<a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">10.1016/j.cattod.2006.11.008</a>.","apa":"Christoffers, J., Werner, T., &#38; Rössle, M. (2007). Cerium-catalyzed oxidative C–C bond forming reactions. <i>Catalysis Today</i>, <i>121</i>(1–2), 22–26. <a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">https://doi.org/10.1016/j.cattod.2006.11.008</a>","ieee":"J. Christoffers, T. Werner, and M. Rössle, “Cerium-catalyzed oxidative C–C bond forming reactions,” <i>Catalysis Today</i>, vol. 121, no. 1–2, pp. 22–26, 2007, doi: <a href=\"https://doi.org/10.1016/j.cattod.2006.11.008\">10.1016/j.cattod.2006.11.008</a>."},"status":"public","volume":121,"user_id":"89271","publisher":"Elsevier BV","_id":"38011","page":"22-26","extern":"1","issue":"1-2","publication":"Catalysis Today","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["General Chemistry","Catalysis"],"date_created":"2023-01-22T21:13:14Z","intvolume":"       121","date_updated":"2025-11-10T09:44:18Z","publication_status":"published","publication_identifier":{"issn":["0920-5861"]},"author":[{"last_name":"Christoffers","first_name":"Jens","full_name":"Christoffers, Jens"},{"id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","full_name":"Werner, Thomas"},{"full_name":"Rössle, Michael","last_name":"Rössle","first_name":"Michael"}],"title":"Cerium-catalyzed oxidative C–C bond forming reactions","year":"2007","doi":"10.1016/j.cattod.2006.11.008","language":[{"iso":"eng"}]},{"citation":{"chicago":"Christoffers, Jens, Thomas Kauf, Thomas Werner, and Michael Rössle. “Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen.” <i>European Journal of Organic Chemistry</i> 2006, no. 11 (2006): 2601–8. <a href=\"https://doi.org/10.1002/ejoc.200600061\">https://doi.org/10.1002/ejoc.200600061</a>.","short":"J. Christoffers, T. Kauf, T. Werner, M. Rössle, European Journal of Organic Chemistry 2006 (2006) 2601–2608.","apa":"Christoffers, J., Kauf, T., Werner, T., &#38; Rössle, M. (2006). Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen. <i>European Journal of Organic Chemistry</i>, <i>2006</i>(11), 2601–2608. <a href=\"https://doi.org/10.1002/ejoc.200600061\">https://doi.org/10.1002/ejoc.200600061</a>","ieee":"J. Christoffers, T. Kauf, T. Werner, and M. Rössle, “Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen,” <i>European Journal of Organic Chemistry</i>, vol. 2006, no. 11, pp. 2601–2608, 2006, doi: <a href=\"https://doi.org/10.1002/ejoc.200600061\">10.1002/ejoc.200600061</a>.","ama":"Christoffers J, Kauf T, Werner T, Rössle M. Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen. <i>European Journal of Organic Chemistry</i>. 2006;2006(11):2601-2608. doi:<a href=\"https://doi.org/10.1002/ejoc.200600061\">10.1002/ejoc.200600061</a>","bibtex":"@article{Christoffers_Kauf_Werner_Rössle_2006, title={Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen}, volume={2006}, DOI={<a href=\"https://doi.org/10.1002/ejoc.200600061\">10.1002/ejoc.200600061</a>}, number={11}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Christoffers, Jens and Kauf, Thomas and Werner, Thomas and Rössle, Michael}, year={2006}, pages={2601–2608} }","mla":"Christoffers, Jens, et al. “Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen.” <i>European Journal of Organic Chemistry</i>, vol. 2006, no. 11, Wiley, 2006, pp. 2601–08, doi:<a href=\"https://doi.org/10.1002/ejoc.200600061\">10.1002/ejoc.200600061</a>."},"status":"public","page":"2601-2608","_id":"38013","publisher":"Wiley","user_id":"14931","volume":2006,"issue":"11","publication":"European Journal of Organic Chemistry","extern":"1","date_created":"2023-01-22T21:13:53Z","type":"journal_article","keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"title":"Cerium-Catalyzed α-Hydroxylation Reactions of α-Cyclopropyl β-Dicarbonyl Compounds with Molecular Oxygen","year":"2006","author":[{"full_name":"Christoffers, Jens","last_name":"Christoffers","first_name":"Jens"},{"full_name":"Kauf, Thomas","last_name":"Kauf","first_name":"Thomas"},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner"},{"first_name":"Michael","last_name":"Rössle","full_name":"Rössle, Michael"}],"publication_identifier":{"issn":["1434-193X","1099-0690"]},"date_updated":"2023-01-23T10:12:18Z","publication_status":"published","intvolume":"      2006","language":[{"iso":"eng"}],"doi":"10.1002/ejoc.200600061"},{"publication":"The Journal of Organic Chemistry","issue":"11","extern":"1","date_created":"2023-01-22T21:13:34Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["Organic Chemistry"],"type":"journal_article","publication_identifier":{"issn":["0022-3263","1520-6904"]},"author":[{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","id":"89271"},{"last_name":"Barrett","first_name":"Anthony G. M.","full_name":"Barrett, Anthony G. M."}],"title":"Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates","year":"2006","intvolume":"        71","date_updated":"2023-01-23T10:12:37Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1021/jo060562m","citation":{"bibtex":"@article{Werner_Barrett_2006, title={Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates}, volume={71}, DOI={<a href=\"https://doi.org/10.1021/jo060562m\">10.1021/jo060562m</a>}, number={11}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Werner, Thomas and Barrett, Anthony G. M.}, year={2006}, pages={4302–4304} }","ama":"Werner T, Barrett AGM. Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates. <i>The Journal of Organic Chemistry</i>. 2006;71(11):4302-4304. doi:<a href=\"https://doi.org/10.1021/jo060562m\">10.1021/jo060562m</a>","mla":"Werner, Thomas, and Anthony G. M. Barrett. “Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates.” <i>The Journal of Organic Chemistry</i>, vol. 71, no. 11, American Chemical Society (ACS), 2006, pp. 4302–04, doi:<a href=\"https://doi.org/10.1021/jo060562m\">10.1021/jo060562m</a>.","short":"T. Werner, A.G.M. Barrett, The Journal of Organic Chemistry 71 (2006) 4302–4304.","chicago":"Werner, Thomas, and Anthony G. M. Barrett. “Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates.” <i>The Journal of Organic Chemistry</i> 71, no. 11 (2006): 4302–4. <a href=\"https://doi.org/10.1021/jo060562m\">https://doi.org/10.1021/jo060562m</a>.","ieee":"T. Werner and A. G. M. Barrett, “Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates,” <i>The Journal of Organic Chemistry</i>, vol. 71, no. 11, pp. 4302–4304, 2006, doi: <a href=\"https://doi.org/10.1021/jo060562m\">10.1021/jo060562m</a>.","apa":"Werner, T., &#38; Barrett, A. G. M. (2006). Simple Method for the Preparation of Esters from Grignard Reagents and Alkyl 1-Imidazolecarboxylates. <i>The Journal of Organic Chemistry</i>, <i>71</i>(11), 4302–4304. <a href=\"https://doi.org/10.1021/jo060562m\">https://doi.org/10.1021/jo060562m</a>"},"status":"public","publisher":"American Chemical Society (ACS)","_id":"38012","page":"4302-4304","volume":71,"user_id":"14931"},{"extern":"1","publication":"European Journal of Organic Chemistry","issue":"23","keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:14:15Z","publication_status":"published","date_updated":"2023-01-23T10:11:45Z","intvolume":"      2005","title":"Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds","year":"2005","publication_identifier":{"issn":["1434-193X","1099-0690"]},"author":[{"full_name":"Rössle, Michael","last_name":"Rössle","first_name":"Michael"},{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","id":"89271"},{"full_name":"Frey, Wolfgang","last_name":"Frey","first_name":"Wolfgang"},{"full_name":"Christoffers, Jens","last_name":"Christoffers","first_name":"Jens"}],"doi":"10.1002/ejoc.200500487","language":[{"iso":"eng"}],"citation":{"mla":"Rössle, Michael, et al. “Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds.” <i>European Journal of Organic Chemistry</i>, vol. 2005, no. 23, Wiley, 2005, pp. 5031–38, doi:<a href=\"https://doi.org/10.1002/ejoc.200500487\">10.1002/ejoc.200500487</a>.","ama":"Rössle M, Werner T, Frey W, Christoffers J. Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds. <i>European Journal of Organic Chemistry</i>. 2005;2005(23):5031-5038. doi:<a href=\"https://doi.org/10.1002/ejoc.200500487\">10.1002/ejoc.200500487</a>","bibtex":"@article{Rössle_Werner_Frey_Christoffers_2005, title={Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds}, volume={2005}, DOI={<a href=\"https://doi.org/10.1002/ejoc.200500487\">10.1002/ejoc.200500487</a>}, number={23}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Rössle, Michael and Werner, Thomas and Frey, Wolfgang and Christoffers, Jens}, year={2005}, pages={5031–5038} }","apa":"Rössle, M., Werner, T., Frey, W., &#38; Christoffers, J. (2005). Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds. <i>European Journal of Organic Chemistry</i>, <i>2005</i>(23), 5031–5038. <a href=\"https://doi.org/10.1002/ejoc.200500487\">https://doi.org/10.1002/ejoc.200500487</a>","ieee":"M. Rössle, T. Werner, W. Frey, and J. Christoffers, “Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds,” <i>European Journal of Organic Chemistry</i>, vol. 2005, no. 23, pp. 5031–5038, 2005, doi: <a href=\"https://doi.org/10.1002/ejoc.200500487\">10.1002/ejoc.200500487</a>.","chicago":"Rössle, Michael, Thomas Werner, Wolfgang Frey, and Jens Christoffers. “Cerium-Catalyzed, Aerobic Oxidative Synthesis of 1,2-Dioxane Derivatives from Styrene and Their Fragmentation into 1,4-Dicarbonyl Compounds.” <i>European Journal of Organic Chemistry</i> 2005, no. 23 (2005): 5031–38. <a href=\"https://doi.org/10.1002/ejoc.200500487\">https://doi.org/10.1002/ejoc.200500487</a>.","short":"M. Rössle, T. Werner, W. Frey, J. Christoffers, European Journal of Organic Chemistry 2005 (2005) 5031–5038."},"status":"public","user_id":"14931","volume":2005,"page":"5031-5038","_id":"38014","publisher":"Wiley"}]