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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>","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>.","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>.","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>"},"_id":"37950","publisher":"Wiley","page":"363-372","volume":14,"user_id":"89271","status":"public"},{"citation":{"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>.","short":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, R. Zalubovskis, Synthesis 53 (2021) 3545–3554.","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>.","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>."},"volume":53,"user_id":"89271","_id":"37946","publisher":"Georg Thieme Verlag KG","page":"3545-3554","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","T4","CSSD"],"date_created":"2023-01-22T20:27:34Z","abstract":[{"lang":"eng","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>"}],"issue":"19","publication":"Synthesis","doi":"10.1055/a-1509-6078","language":[{"iso":"eng"}],"intvolume":"        53","date_updated":"2025-11-10T08:47:47Z","publication_status":"published","publication_identifier":{"issn":["0039-7881","1437-210X"]},"author":[{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"},{"full_name":"Grandane, Aiga","last_name":"Grandane","first_name":"Aiga"},{"first_name":"Linda","last_name":"Pudnika","full_name":"Pudnika, Linda"},{"first_name":"Ilona","last_name":"Domraceva","full_name":"Domraceva, Ilona"},{"last_name":"Zalubovskis","first_name":"Raivis","full_name":"Zalubovskis, Raivis"}],"year":"2021","title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones"},{"citation":{"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>.","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>.","short":"X. Liu, T. Werner, Chemical Science 12 (2021) 10590–10597.","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>"},"status":"public","page":"10590-10597","publisher":"Royal Society of Chemistry (RSC)","_id":"37944","user_id":"89271","volume":12,"issue":"31","publication":"Chemical Science","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"}],"date_created":"2023-01-22T20:24:03Z","type":"journal_article","keyword":["T1","T3","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"title":"Indirect reduction of CO<sub>2</sub> and recycling of polymers by manganese-catalyzed transfer hydrogenation of amides, carbamates, urea derivatives, and polyurethanes","year":"2021","author":[{"full_name":"Liu, Xin","first_name":"Xin","last_name":"Liu"},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner"}],"publication_identifier":{"issn":["2041-6520","2041-6539"]},"publication_status":"published","date_updated":"2025-11-10T08:49:01Z","intvolume":"        12","language":[{"iso":"eng"}],"doi":"10.1039/d1sc02663a"},{"language":[{"iso":"eng"}],"doi":"10.1039/d1gc00953b","title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","year":"2021","author":[{"last_name":"Tönjes","first_name":"Jan","full_name":"Tönjes, Jan"},{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","date_updated":"2025-11-10T08:48:01Z","intvolume":"        23","date_created":"2023-01-22T20:25:13Z","keyword":["T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"publication":"Green Chemistry","issue":"13","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"}],"page":"4852-4857","publisher":"Royal Society of Chemistry (RSC)","_id":"37945","user_id":"89271","volume":23,"status":"public","citation":{"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} }","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.","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>.","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>.","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>"}},{"volume":225,"user_id":"89271","_id":"37943","publisher":"Elsevier BV","status":"public","citation":{"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. Werner, Ecotoxicology and Environmental Safety 225 (2021).","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>"},"doi":"10.1016/j.ecoenv.2021.112768","language":[{"iso":"eng"}],"article_number":"112768","intvolume":"       225","publication_status":"published","date_updated":"2025-11-10T08:48:20Z","publication_identifier":{"issn":["0147-6513"]},"author":[{"first_name":"Marisa A.","last_name":"Wirth","full_name":"Wirth, Marisa A."},{"last_name":"Longwitz","first_name":"Lars","full_name":"Longwitz, Lars"},{"full_name":"Kanwischer, Marion","first_name":"Marion","last_name":"Kanwischer"},{"full_name":"Gros, Peter","first_name":"Peter","last_name":"Gros"},{"first_name":"Peter","last_name":"Leinweber","full_name":"Leinweber, Peter"},{"first_name":"Thomas","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"year":"2021","title":"AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T4","CSSD"],"date_created":"2023-01-22T20:23:06Z","publication":"Ecotoxicology and Environmental Safety"},{"citation":{"ama":"Liu X, Werner T. Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides. <i>Advanced Synthesis and Catalysis</i>. 2021;363(4):1096-1104. doi:<a href=\"https://doi.org/10.1002/adsc.202001209\">10.1002/adsc.202001209</a>","bibtex":"@article{Liu_Werner_2021, title={Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides}, volume={363}, DOI={<a href=\"https://doi.org/10.1002/adsc.202001209\">10.1002/adsc.202001209</a>}, number={4}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Liu, Xin and Werner, Thomas}, year={2021}, pages={1096–1104} }","mla":"Liu, Xin, and Thomas Werner. “Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides.” <i>Advanced Synthesis and Catalysis</i>, vol. 363, no. 4, Wiley, 2021, pp. 1096–104, doi:<a href=\"https://doi.org/10.1002/adsc.202001209\">10.1002/adsc.202001209</a>.","chicago":"Liu, Xin, and Thomas Werner. “Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides.” <i>Advanced Synthesis and Catalysis</i> 363, no. 4 (2021): 1096–1104. <a href=\"https://doi.org/10.1002/adsc.202001209\">https://doi.org/10.1002/adsc.202001209</a>.","short":"X. Liu, T. Werner, Advanced Synthesis and Catalysis 363 (2021) 1096–1104.","apa":"Liu, X., &#38; Werner, T. (2021). Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides. <i>Advanced Synthesis and Catalysis</i>, <i>363</i>(4), 1096–1104. <a href=\"https://doi.org/10.1002/adsc.202001209\">https://doi.org/10.1002/adsc.202001209</a>","ieee":"X. Liu and T. Werner, “Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides,” <i>Advanced Synthesis and Catalysis</i>, vol. 363, no. 4, pp. 1096–1104, 2021, doi: <a href=\"https://doi.org/10.1002/adsc.202001209\">10.1002/adsc.202001209</a>."},"page":"1096-1104","publisher":"Wiley","_id":"37948","user_id":"89271","volume":363,"status":"public","date_created":"2023-01-22T20:30:29Z","keyword":["T1","T3","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"publication":"Advanced Synthesis and Catalysis","issue":"4","extern":"1","language":[{"iso":"eng"}],"doi":"10.1002/adsc.202001209","year":"2021","title":"Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides","publication_identifier":{"issn":["1615-4150","1615-4169"]},"author":[{"full_name":"Liu, Xin","first_name":"Xin","last_name":"Liu"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","full_name":"Werner, Thomas"}],"date_updated":"2025-11-10T08:48:47Z","publication_status":"published","intvolume":"       363"},{"volume":68,"user_id":"89271","publisher":"Wiley","_id":"37956","page":"42-72","status":"public","citation":{"ieee":"J. N. Andexer <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 68, no. 3, pp. 42–72, 2020, doi: <a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>.","apa":"Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Greb, J., Gulder, T., Hüttel, W., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle, C., Narine, A., Niemeyer, J., Paradies, J., … Winter, C. (2020). Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>68</i>(3), 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>","short":"J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, J. Greb, T. Gulder, W. Hüttel, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle, A. Narine, J. Niemeyer, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 68 (2020) 42–72.","chicago":"Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Julian Greb, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 68, no. 3 (2020): 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>.","mla":"Andexer, Jennifer N., et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 68, no. 3, Wiley, 2020, pp. 42–72, doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>.","bibtex":"@article{Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Greb_Gulder_Hüttel_Kath‐Schorr_et al._2020, title={Organische Chemie}, volume={68}, DOI={<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Greb, Julian and Gulder, Tobias and Hüttel, Wolfgang and Kath‐Schorr, Stephanie and et al.}, year={2020}, pages={42–72} }","ama":"Andexer JN, Beifuss U, Beuerle F, et al. 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Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature. <i>ACS Catalysis</i>. 2019;9(10):9237-9244. doi:<a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>","chicago":"Longwitz, Lars, Anke Spannenberg, and Thomas Werner. “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature.” <i>ACS Catalysis</i> 9, no. 10 (2019): 9237–44. <a href=\"https://doi.org/10.1021/acscatal.9b02456\">https://doi.org/10.1021/acscatal.9b02456</a>.","bibtex":"@article{Longwitz_Spannenberg_Werner_2019, title={Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature}, volume={9}, DOI={<a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>}, number={10}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Spannenberg, Anke and Werner, Thomas}, year={2019}, pages={9237–9244} }"}},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["General Chemical Engineering","General Chemistry"],"date_created":"2023-01-22T20:44:46Z","issue":"3","publication":"Nachrichten aus der Chemie","doi":"10.1002/nadc.20194085243","language":[{"iso":"eng"}],"intvolume":"        67","publication_status":"published","date_updated":"2025-11-10T08:57:09Z","author":[{"full_name":"Andexer, Jennifer N.","last_name":"Andexer","first_name":"Jennifer N."},{"full_name":"Beifuss, Uwe","first_name":"Uwe","last_name":"Beifuss"},{"first_name":"Florian","last_name":"Beuerle","full_name":"Beuerle, Florian"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"first_name":"Martin","last_name":"Ernst","full_name":"Ernst, Martin"},{"last_name":"Gulder","first_name":"Tobias A. 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Trendbericht Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2019;67(3):46-78. doi:<a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>","bibtex":"@article{Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Gulder_Kath‐Schorr_Kordes_Lehmann_et al._2019, title={Trendbericht Organische Chemie}, volume={67}, DOI={<a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Gulder, Tobias A. M. and Kath‐Schorr, Stephanie and Kordes, Markus and Lehmann, Matthias and et al.}, year={2019}, pages={46–78} }","mla":"Andexer, Jennifer N., et al. “Trendbericht Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 67, no. 3, Wiley, 2019, pp. 46–78, doi:<a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>.","short":"J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, T.A.M. Gulder, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, S. Lüdeke, B. Luy, M. Mantel, C. Mück‐Lichtenfeld, C. Muhle‐Goll, A. Narine, J. Niemeyer, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 67 (2019) 46–78.","chicago":"Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Tobias A. M. Gulder, et al. “Trendbericht Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 67, no. 3 (2019): 46–78. <a href=\"https://doi.org/10.1002/nadc.20194085243\">https://doi.org/10.1002/nadc.20194085243</a>.","apa":"Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Gulder, T. A. M., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Lüdeke, S., Luy, B., Mantel, M., Mück‐Lichtenfeld, C., Muhle‐Goll, C., Narine, A., Niemeyer, J., Pfau, R., … Winter, C. (2019). Trendbericht Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>67</i>(3), 46–78. <a href=\"https://doi.org/10.1002/nadc.20194085243\">https://doi.org/10.1002/nadc.20194085243</a>","ieee":"J. N. Andexer <i>et al.</i>, “Trendbericht Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 67, no. 3, pp. 46–78, 2019, doi: <a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>."},"volume":67,"user_id":"89271","_id":"37964","publisher":"Wiley","page":"46-78","status":"public"},{"publication_status":"published","date_updated":"2025-11-10T08:55:06Z","intvolume":"        21","title":"Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts","year":"2019","author":[{"full_name":"Liu, Xin","first_name":"Xin","last_name":"Liu"},{"last_name":"de Vries","first_name":"Johannes G.","full_name":"de Vries, Johannes G."},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"doi":"10.1039/c9gc02052g","language":[{"iso":"eng"}],"extern":"1","abstract":[{"text":"<p>The reduction of poly and cyclic carbonates in the presence of an earth abundant metal catalyst using isopropanol as the hydrogen donor is reported.</p>","lang":"eng"}],"publication":"Green Chemistry","issue":"19","keyword":["T3","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:43:38Z","status":"public","user_id":"89271","volume":21,"page":"5248-5255","publisher":"Royal Society of Chemistry (RSC)","_id":"37961","citation":{"bibtex":"@article{Liu_de Vries_Werner_2019, title={Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts}, volume={21}, DOI={<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>}, number={19}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Liu, Xin and de Vries, Johannes G. and Werner, Thomas}, year={2019}, pages={5248–5255} }","ama":"Liu X, de Vries JG, Werner T. Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>. 2019;21(19):5248-5255. doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>","mla":"Liu, Xin, et al. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i>, vol. 21, no. 19, Royal Society of Chemistry (RSC), 2019, pp. 5248–55, doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","short":"X. Liu, J.G. de Vries, T. Werner, Green Chemistry 21 (2019) 5248–5255.","chicago":"Liu, Xin, Johannes G. de Vries, and Thomas Werner. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i> 21, no. 19 (2019): 5248–55. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>.","ieee":"X. Liu, J. G. de Vries, and T. Werner, “Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts,” <i>Green Chemistry</i>, vol. 21, no. 19, pp. 5248–5255, 2019, doi: <a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","apa":"Liu, X., de Vries, J. G., &#38; Werner, T. (2019). Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>, <i>21</i>(19), 5248–5255. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>"}},{"extern":"1","publication":"ChemSusChem","issue":"12","type":"journal_article","keyword":["T1","T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:44:24Z","publication_status":"published","date_updated":"2025-11-10T08:56:56Z","intvolume":"        12","year":"2019","title":"Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"full_name":"Büttner, Hendrik","first_name":"Hendrik","last_name":"Büttner"},{"full_name":"Kohrt, Christina","last_name":"Kohrt","first_name":"Christina"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"full_name":"Schäffner, Benjamin","last_name":"Schäffner","first_name":"Benjamin"},{"last_name":"Groenke","first_name":"Karsten","full_name":"Groenke, Karsten"},{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"last_name":"Kruse","first_name":"Daniela","full_name":"Kruse, Daniela"},{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","id":"89271"}],"doi":"10.1002/cssc.201900678","language":[{"iso":"eng"}],"citation":{"mla":"Büttner, Hendrik, et al. “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i>, vol. 12, no. 12, Wiley, 2019, pp. 2701–07, doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>.","apa":"Büttner, H., Kohrt, C., Wulf, C., Schäffner, B., Groenke, K., Hu, Y., Kruse, D., &#38; Werner, T. 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Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>. 2019;12(12):2701-2707. doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>","bibtex":"@article{Büttner_Kohrt_Wulf_Schäffner_Groenke_Hu_Kruse_Werner_2019, title={Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate}, volume={12}, DOI={<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>}, number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke, Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}, year={2019}, pages={2701–2707} }"},"status":"public","user_id":"89271","volume":12,"page":"2701-2707","_id":"37963","publisher":"Wiley"},{"citation":{"mla":"Hu, Yuya, et al. “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 7, no. 15, American Chemical Society (ACS), 2019, pp. 13257–69, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>.","bibtex":"@article{Hu_Steinbauer_Stefanow_Spannenberg_Werner_2019, title={Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis}, volume={7}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>}, number={15}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Hu, Yuya and Steinbauer, Johannes and Stefanow, Vivian and Spannenberg, Anke and Werner, Thomas}, year={2019}, pages={13257–13269} }","ama":"Hu Y, Steinbauer J, Stefanow V, Spannenberg A, Werner T. Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ACS Sustainable Chemistry and Engineering</i>. 2019;7(15):13257-13269. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>","ieee":"Y. Hu, J. Steinbauer, V. Stefanow, A. Spannenberg, and T. Werner, “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 7, no. 15, pp. 13257–13269, 2019, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">10.1021/acssuschemeng.9b02502</a>.","apa":"Hu, Y., Steinbauer, J., Stefanow, V., Spannenberg, A., &#38; Werner, T. (2019). 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