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Altering of lower critical solution temperature of environmentally responsive poly (N-isopropylacrylamide-co-acrylic acid-co-vanillin acrylate) affected by acrylic acid, vanillin acrylate, and post-polymerization modification. <i>Colloid and Polymer Science</i>, <i>299</i>(10), 1617–1629. <a href=\"https://doi.org/10.1007/s00396-021-04882-x\">https://doi.org/10.1007/s00396-021-04882-x</a>","ieee":"M. S. A. Abdelaty and D. Kuckling, “Altering of lower critical solution temperature of environmentally responsive poly (N-isopropylacrylamide-co-acrylic acid-co-vanillin acrylate) affected by acrylic acid, vanillin acrylate, and post-polymerization modification,” <i>Colloid and Polymer Science</i>, vol. 299, no. 10, pp. 1617–1629, 2021, doi: <a href=\"https://doi.org/10.1007/s00396-021-04882-x\">10.1007/s00396-021-04882-x</a>.","chicago":"Abdelaty, Momen S. 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Paradies, J. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, R. Ganardi, T.A.M. Gulder, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle‐Goll, J. Niemeyer, R. Pfau, J. Pietruszka, J.L. Röckl, N. Schaschke, M.O. Senge, B.F. Straub, S.R. Waldvogel, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 69 (2021) 38–68.","chicago":"Paradies, Jan, Jennifer Andexer, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 69, no. 3 (2021): 38–68. <a href=\"https://doi.org/10.1002/nadc.20214105947\">https://doi.org/10.1002/nadc.20214105947</a>.","ieee":"J. Paradies <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 69, no. 3, pp. 38–68, 2021, doi: <a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>.","apa":"Paradies, J., Andexer, J., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Ganardi, R., Gulder, T. A. M., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle‐Goll, C., Niemeyer, J., … Winter, C. (2021). Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>69</i>(3), 38–68. <a href=\"https://doi.org/10.1002/nadc.20214105947\">https://doi.org/10.1002/nadc.20214105947</a>","bibtex":"@article{Paradies_Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Ganardi_Gulder_Hüttel_et al._2021, title={Organische Chemie}, volume={69}, DOI={<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Paradies, Jan and Andexer, Jennifer and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Ganardi, Ruth and Gulder, Tobias A. M. and Hüttel, Wolfgang and et al.}, year={2021}, pages={38–68} }","ama":"Paradies J, Andexer J, Beifuss U, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2021;69(3):38-68. doi:<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>","mla":"Paradies, Jan, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 69, no. 3, Wiley, 2021, pp. 38–68, doi:<a href=\"https://doi.org/10.1002/nadc.20214105947\">10.1002/nadc.20214105947</a>."},"doi":"10.1002/nadc.20214105947","language":[{"iso":"eng"}],"intvolume":"        69","date_updated":"2025-11-10T08:02:44Z","publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]},"author":[{"id":"53339","first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan"},{"last_name":"Andexer","first_name":"Jennifer","full_name":"Andexer, Jennifer"},{"full_name":"Beifuss, Uwe","first_name":"Uwe","last_name":"Beifuss"},{"full_name":"Beuerle, Florian","first_name":"Florian","last_name":"Beuerle"},{"full_name":"Brasholz, Malte","first_name":"Malte","last_name":"Brasholz"},{"full_name":"Breinbauer, Rolf","first_name":"Rolf","last_name":"Breinbauer"},{"last_name":"Ernst","first_name":"Martin","full_name":"Ernst, Martin"},{"first_name":"Ruth","last_name":"Ganardi","full_name":"Ganardi, Ruth"},{"last_name":"Gulder","first_name":"Tobias A. M.","full_name":"Gulder, Tobias A. M."},{"first_name":"Wolfgang","last_name":"Hüttel","full_name":"Hüttel, Wolfgang"},{"full_name":"Kath‐Schorr, Stephanie","first_name":"Stephanie","last_name":"Kath‐Schorr"},{"full_name":"Körber, Karsten","last_name":"Körber","first_name":"Karsten"},{"full_name":"Kordes, Markus","first_name":"Markus","last_name":"Kordes"},{"full_name":"Lehmann, Matthias","last_name":"Lehmann","first_name":"Matthias"},{"full_name":"Lindel, Thomas","first_name":"Thomas","last_name":"Lindel"},{"full_name":"Luy, Burkhard","first_name":"Burkhard","last_name":"Luy"},{"first_name":"Christian","last_name":"Mück‐Lichtenfeld","full_name":"Mück‐Lichtenfeld, Christian"},{"full_name":"Muhle‐Goll, Claudia","first_name":"Claudia","last_name":"Muhle‐Goll"},{"full_name":"Niemeyer, Jochen","first_name":"Jochen","last_name":"Niemeyer"},{"first_name":"Roland","last_name":"Pfau","full_name":"Pfau, Roland"},{"last_name":"Pietruszka","first_name":"Jörg","full_name":"Pietruszka, Jörg"},{"full_name":"Röckl, Johannes L.","first_name":"Johannes L.","last_name":"Röckl"},{"first_name":"Norbert","last_name":"Schaschke","full_name":"Schaschke, Norbert"},{"full_name":"Senge, Mathias O.","last_name":"Senge","first_name":"Mathias O."},{"first_name":"Bernd F.","last_name":"Straub","full_name":"Straub, Bernd F."},{"full_name":"Waldvogel, Siegfried R.","first_name":"Siegfried R.","last_name":"Waldvogel"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"full_name":"Winter, Christian","last_name":"Winter","first_name":"Christian"}],"year":"2021","title":"Organische Chemie","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["General Chemical Engineering","General Chemistry"],"date_created":"2023-01-22T20:28:35Z","publication":"Nachrichten aus der Chemie","issue":"3"},{"citation":{"short":"Y. Hu, Z. Wei, A. Frey, C. Kubis, C. Ren, A. Spannenberg, H. Jiao, T. Werner, ChemSusChem 14 (2021) 363–372.","chicago":"Hu, Yuya, Zhihong Wei, Anna Frey, Christoph Kubis, Chang‐Yue Ren, Anke Spannenberg, Haijun Jiao, and Thomas Werner. “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts.” <i>ChemSusChem</i> 14, no. 1 (2021): 363–72. <a href=\"https://doi.org/10.1002/cssc.202002267\">https://doi.org/10.1002/cssc.202002267</a>.","ieee":"Y. Hu <i>et al.</i>, “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts,” <i>ChemSusChem</i>, vol. 14, no. 1, pp. 363–372, 2021, doi: <a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>.","apa":"Hu, Y., Wei, Z., Frey, A., Kubis, C., Ren, C., Spannenberg, A., Jiao, H., &#38; Werner, T. (2021). Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts. <i>ChemSusChem</i>, <i>14</i>(1), 363–372. <a href=\"https://doi.org/10.1002/cssc.202002267\">https://doi.org/10.1002/cssc.202002267</a>","bibtex":"@article{Hu_Wei_Frey_Kubis_Ren_Spannenberg_Jiao_Werner_2021, title={Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts}, volume={14}, DOI={<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>}, number={1}, journal={ChemSusChem}, publisher={Wiley}, author={Hu, Yuya and Wei, Zhihong and Frey, Anna and Kubis, Christoph and Ren, Chang‐Yue and Spannenberg, Anke and Jiao, Haijun and Werner, Thomas}, year={2021}, pages={363–372} }","ama":"Hu Y, Wei Z, Frey A, et al. Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts. <i>ChemSusChem</i>. 2021;14(1):363-372. doi:<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>","mla":"Hu, Yuya, et al. “Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts.” <i>ChemSusChem</i>, vol. 14, no. 1, Wiley, 2021, pp. 363–72, doi:<a href=\"https://doi.org/10.1002/cssc.202002267\">10.1002/cssc.202002267</a>."},"status":"public","volume":14,"user_id":"89271","_id":"37950","publisher":"Wiley","page":"363-372","extern":"1","issue":"1","publication":"ChemSusChem","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1"],"date_created":"2023-01-22T20:34:17Z","intvolume":"        14","publication_status":"published","date_updated":"2025-11-10T08:04:27Z","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"first_name":"Yuya","last_name":"Hu","full_name":"Hu, Yuya"},{"full_name":"Wei, Zhihong","last_name":"Wei","first_name":"Zhihong"},{"last_name":"Frey","first_name":"Anna","full_name":"Frey, Anna"},{"last_name":"Kubis","first_name":"Christoph","full_name":"Kubis, Christoph"},{"last_name":"Ren","first_name":"Chang‐Yue","full_name":"Ren, Chang‐Yue"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"full_name":"Jiao, Haijun","first_name":"Haijun","last_name":"Jiao"},{"orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"year":"2021","title":"Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts","doi":"10.1002/cssc.202002267","language":[{"iso":"eng"}]},{"user_id":"89271","volume":53,"page":"3545-3554","publisher":"Georg Thieme Verlag KG","_id":"37946","status":"public","citation":{"ama":"Werner T, Grandane A, Pudnika L, Domraceva I, Zalubovskis R. Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>. 2021;53(19):3545-3554. doi:<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>","bibtex":"@article{Werner_Grandane_Pudnika_Domraceva_Zalubovskis_2021, title={Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones}, volume={53}, DOI={<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>}, number={19}, journal={Synthesis}, publisher={Georg Thieme Verlag KG}, author={Werner, Thomas and Grandane, Aiga and Pudnika, Linda and Domraceva, Ilona and Zalubovskis, Raivis}, year={2021}, pages={3545–3554} }","mla":"Werner, Thomas, et al. “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones.” <i>Synthesis</i>, vol. 53, no. 19, Georg Thieme Verlag KG, 2021, pp. 3545–54, doi:<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>.","short":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, R. Zalubovskis, Synthesis 53 (2021) 3545–3554.","chicago":"Werner, Thomas, Aiga Grandane, Linda Pudnika, Ilona Domraceva, and Raivis Zalubovskis. “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones.” <i>Synthesis</i> 53, no. 19 (2021): 3545–54. <a href=\"https://doi.org/10.1055/a-1509-6078\">https://doi.org/10.1055/a-1509-6078</a>.","apa":"Werner, T., Grandane, A., Pudnika, L., Domraceva, I., &#38; Zalubovskis, R. (2021). Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>, <i>53</i>(19), 3545–3554. <a href=\"https://doi.org/10.1055/a-1509-6078\">https://doi.org/10.1055/a-1509-6078</a>","ieee":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, and R. Zalubovskis, “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones,” <i>Synthesis</i>, vol. 53, no. 19, pp. 3545–3554, 2021, doi: <a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>."},"doi":"10.1055/a-1509-6078","language":[{"iso":"eng"}],"publication_status":"published","date_updated":"2025-11-10T08:47:47Z","intvolume":"        53","title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones","year":"2021","author":[{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"full_name":"Grandane, Aiga","first_name":"Aiga","last_name":"Grandane"},{"full_name":"Pudnika, Linda","first_name":"Linda","last_name":"Pudnika"},{"full_name":"Domraceva, Ilona","first_name":"Ilona","last_name":"Domraceva"},{"full_name":"Zalubovskis, Raivis","last_name":"Zalubovskis","first_name":"Raivis"}],"publication_identifier":{"issn":["0039-7881","1437-210X"]},"type":"journal_article","keyword":["T2","T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:27:34Z","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The facile synthesis of highly functionalized building blocks with potential biological activity is of great interest to medicinal chemistry. The benzoxepinone core structures commonly exhibit biological activity. Thus, a short and efficient synthetic route towards benzoxepine containing scaffold, which enables late stage modification was developed. Namely, base-free catalytic Wittig reactions enabled the synthesis of bromobenzoxepinones from readily available starting materials. Subsequent, Suzuki–Miyaura and Stille reactions proved to be suitable methods to access a variety of benzoxepinone diaryl derivatives by late stage modification in only three steps. This three-step reaction sequence is suitable for high throughput applications and gives facile access to highly complex molecular structures, which are suitable for further functionalization. The antiproliferative properties of selected arylbenzoxepinones­ were tested in vitro on monolayer tumor cell line A549. Notably, in this initial screening, these compounds were found to be active in the micromolar range.</jats:p>","lang":"eng"}],"publication":"Synthesis","issue":"19"},{"status":"public","volume":12,"user_id":"89271","publisher":"Royal Society of Chemistry (RSC)","_id":"37944","page":"10590-10597","citation":{"short":"X. Liu, T. Werner, Chemical Science 12 (2021) 10590–10597.","chicago":"Liu, Xin, and Thomas Werner. “Indirect Reduction of CO<sub>2</sub> and Recycling of Polymers by Manganese-Catalyzed Transfer Hydrogenation of Amides, Carbamates, Urea Derivatives, and Polyurethanes.” <i>Chemical Science</i> 12, no. 31 (2021): 10590–97. <a href=\"https://doi.org/10.1039/d1sc02663a\">https://doi.org/10.1039/d1sc02663a</a>.","ieee":"X. Liu and T. Werner, “Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes,” <i>Chemical Science</i>, vol. 12, no. 31, pp. 10590–10597, 2021, doi: <a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>.","apa":"Liu, X., &#38; Werner, T. (2021). Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes. <i>Chemical Science</i>, <i>12</i>(31), 10590–10597. <a href=\"https://doi.org/10.1039/d1sc02663a\">https://doi.org/10.1039/d1sc02663a</a>","bibtex":"@article{Liu_Werner_2021, title={Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes}, volume={12}, DOI={<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>}, number={31}, journal={Chemical Science}, publisher={Royal Society of Chemistry (RSC)}, author={Liu, Xin and Werner, Thomas}, year={2021}, pages={10590–10597} }","ama":"Liu X, Werner T. Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes. <i>Chemical Science</i>. 2021;12(31):10590-10597. doi:<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>","mla":"Liu, Xin, and Thomas Werner. “Indirect Reduction of CO<sub>2</sub> and Recycling of Polymers by Manganese-Catalyzed Transfer Hydrogenation of Amides, Carbamates, Urea Derivatives, and Polyurethanes.” <i>Chemical Science</i>, vol. 12, no. 31, Royal Society of Chemistry (RSC), 2021, pp. 10590–97, doi:<a href=\"https://doi.org/10.1039/d1sc02663a\">10.1039/d1sc02663a</a>."},"intvolume":"        12","date_updated":"2025-11-10T08:49:01Z","publication_status":"published","publication_identifier":{"issn":["2041-6520","2041-6539"]},"author":[{"full_name":"Liu, Xin","last_name":"Liu","first_name":"Xin"},{"first_name":"Thomas","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"year":"2021","title":"Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes","doi":"10.1039/d1sc02663a","language":[{"iso":"eng"}],"abstract":[{"text":"<p>A Mn–PNP complex proved to be a suitable catalyst for the transfer hydrogenation of amides, carbamates, urea derivatives and even polyurethanes.</p>","lang":"eng"}],"publication":"Chemical Science","issue":"31","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:24:03Z"},{"status":"public","_id":"37945","publisher":"Royal Society of Chemistry (RSC)","page":"4852-4857","volume":23,"user_id":"89271","citation":{"mla":"Tönjes, Jan, et al. “Poly(Methylhydrosiloxane) as a Reductant in the Catalytic Base-Free Wittig Reaction.” <i>Green Chemistry</i>, vol. 23, no. 13, Royal Society of Chemistry (RSC), 2021, pp. 4852–57, doi:<a href=\"https://doi.org/10.1039/d1gc00953b\">10.1039/d1gc00953b</a>.","apa":"Tönjes, J., Longwitz, L., &#38; Werner, T. (2021). Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction. <i>Green Chemistry</i>, <i>23</i>(13), 4852–4857. <a href=\"https://doi.org/10.1039/d1gc00953b\">https://doi.org/10.1039/d1gc00953b</a>","ieee":"J. Tönjes, L. Longwitz, and T. Werner, “Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction,” <i>Green Chemistry</i>, vol. 23, no. 13, pp. 4852–4857, 2021, doi: <a href=\"https://doi.org/10.1039/d1gc00953b\">10.1039/d1gc00953b</a>.","chicago":"Tönjes, Jan, Lars Longwitz, and Thomas Werner. “Poly(Methylhydrosiloxane) as a Reductant in the Catalytic Base-Free Wittig Reaction.” <i>Green Chemistry</i> 23, no. 13 (2021): 4852–57. <a href=\"https://doi.org/10.1039/d1gc00953b\">https://doi.org/10.1039/d1gc00953b</a>.","ama":"Tönjes J, Longwitz L, Werner T. Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction. <i>Green Chemistry</i>. 2021;23(13):4852-4857. doi:<a href=\"https://doi.org/10.1039/d1gc00953b\">10.1039/d1gc00953b</a>","short":"J. Tönjes, L. Longwitz, T. Werner, Green Chemistry 23 (2021) 4852–4857.","bibtex":"@article{Tönjes_Longwitz_Werner_2021, title={Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction}, volume={23}, DOI={<a href=\"https://doi.org/10.1039/d1gc00953b\">10.1039/d1gc00953b</a>}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tönjes, Jan and Longwitz, Lars and Werner, Thomas}, year={2021}, pages={4852–4857} }"},"publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"full_name":"Tönjes, Jan","first_name":"Jan","last_name":"Tönjes"},{"last_name":"Longwitz","first_name":"Lars","full_name":"Longwitz, Lars"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner"}],"title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","year":"2021","intvolume":"        23","date_updated":"2025-11-10T08:48:01Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1039/d1gc00953b","issue":"13","publication":"Green Chemistry","abstract":[{"text":"<p>PMHS proved to be a suitable terminal reductant for P(<sc>iii</sc>)/P(<sc>v</sc>) redox cycling with a methyl-substituted phosphetane as catalyst and BuOAc as solvent. The formation of water by silanol condensation was identified as main pathway of siloxane formation.</p>","lang":"eng"}],"date_created":"2023-01-22T20:25:13Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"]},{"citation":{"mla":"Wirth, Marisa A., et al. “AMPA-15N – Synthesis and Application as Standard Compound in Traceable Degradation Studies of Glyphosate.” <i>Ecotoxicology and Environmental Safety</i>, vol. 225, 112768, Elsevier BV, 2021, doi:<a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">10.1016/j.ecoenv.2021.112768</a>.","bibtex":"@article{Wirth_Longwitz_Kanwischer_Gros_Leinweber_Werner_2021, title={AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate}, volume={225}, DOI={<a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">10.1016/j.ecoenv.2021.112768</a>}, number={112768}, journal={Ecotoxicology and Environmental Safety}, publisher={Elsevier BV}, author={Wirth, Marisa A. and Longwitz, Lars and Kanwischer, Marion and Gros, Peter and Leinweber, Peter and Werner, Thomas}, year={2021} }","ama":"Wirth MA, Longwitz L, Kanwischer M, Gros P, Leinweber P, Werner T. AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate. <i>Ecotoxicology and Environmental Safety</i>. 2021;225. doi:<a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">10.1016/j.ecoenv.2021.112768</a>","ieee":"M. A. Wirth, L. Longwitz, M. Kanwischer, P. Gros, P. Leinweber, and T. Werner, “AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate,” <i>Ecotoxicology and Environmental Safety</i>, vol. 225, Art. no. 112768, 2021, doi: <a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">10.1016/j.ecoenv.2021.112768</a>.","apa":"Wirth, M. A., Longwitz, L., Kanwischer, M., Gros, P., Leinweber, P., &#38; Werner, T. (2021). AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate. <i>Ecotoxicology and Environmental Safety</i>, <i>225</i>, Article 112768. <a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">https://doi.org/10.1016/j.ecoenv.2021.112768</a>","chicago":"Wirth, Marisa A., Lars Longwitz, Marion Kanwischer, Peter Gros, Peter Leinweber, and Thomas Werner. “AMPA-15N – Synthesis and Application as Standard Compound in Traceable Degradation Studies of Glyphosate.” <i>Ecotoxicology and Environmental Safety</i> 225 (2021). <a href=\"https://doi.org/10.1016/j.ecoenv.2021.112768\">https://doi.org/10.1016/j.ecoenv.2021.112768</a>.","short":"M.A. Wirth, L. Longwitz, M. Kanwischer, P. Gros, P. Leinweber, T. 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Novel Application of Polymer Networks Carrying Tertiary Amines as a Catalyst Inside Microflow Reactors Used for            Knoevenagel            Reactions. <i>European Journal of Organic Chemistry</i>. 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