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Hu, Z. Wei, A. Frey, C. Kubis, C. Ren, A. Spannenberg, H. Jiao, T. Werner, ChemSusChem 14 (2021) 363–372.","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","_id":"37950","publisher":"Wiley","page":"363-372","volume":14,"user_id":"89271","publication":"ChemSusChem","issue":"1","extern":"1","date_created":"2023-01-22T20:34:17Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1"],"type":"journal_article","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"full_name":"Hu, Yuya","first_name":"Yuya","last_name":"Hu"},{"last_name":"Wei","first_name":"Zhihong","full_name":"Wei, Zhihong"},{"last_name":"Frey","first_name":"Anna","full_name":"Frey, Anna"},{"last_name":"Kubis","first_name":"Christoph","full_name":"Kubis, Christoph"},{"full_name":"Ren, Chang‐Yue","first_name":"Chang‐Yue","last_name":"Ren"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Haijun","last_name":"Jiao","full_name":"Jiao, Haijun"},{"orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"title":"Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts","year":"2021","intvolume":"        14","publication_status":"published","date_updated":"2025-11-10T08:04:27Z","language":[{"iso":"eng"}],"doi":"10.1002/cssc.202002267"},{"_id":"37946","publisher":"Georg Thieme Verlag KG","page":"3545-3554","volume":53,"user_id":"89271","status":"public","citation":{"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} }","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>","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>.","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>.","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>"},"language":[{"iso":"eng"}],"doi":"10.1055/a-1509-6078","publication_identifier":{"issn":["0039-7881","1437-210X"]},"author":[{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"last_name":"Grandane","first_name":"Aiga","full_name":"Grandane, Aiga"},{"last_name":"Pudnika","first_name":"Linda","full_name":"Pudnika, Linda"},{"full_name":"Domraceva, Ilona","last_name":"Domraceva","first_name":"Ilona"},{"full_name":"Zalubovskis, Raivis","last_name":"Zalubovskis","first_name":"Raivis"}],"title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones","year":"2021","intvolume":"        53","date_updated":"2025-11-10T08:47:47Z","publication_status":"published","date_created":"2023-01-22T20:27:34Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","T4","CSSD"],"issue":"19","publication":"Synthesis","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>"}]},{"volume":12,"user_id":"89271","_id":"37944","publisher":"Royal Society of Chemistry (RSC)","page":"10590-10597","status":"public","citation":{"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>","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>."},"doi":"10.1039/d1sc02663a","language":[{"iso":"eng"}],"intvolume":"        12","publication_status":"published","date_updated":"2025-11-10T08:49:01Z","author":[{"full_name":"Liu, Xin","first_name":"Xin","last_name":"Liu"},{"orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["2041-6520","2041-6539"]},"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","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T20:24:03Z","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"},{"doi":"10.1039/d1gc00953b","language":[{"iso":"eng"}],"intvolume":"        23","publication_status":"published","date_updated":"2025-11-10T08:48:01Z","author":[{"full_name":"Tönjes, Jan","last_name":"Tönjes","first_name":"Jan"},{"full_name":"Longwitz, Lars","first_name":"Lars","last_name":"Longwitz"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"year":"2021","title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:25:13Z","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"}],"issue":"13","publication":"Green Chemistry","volume":23,"user_id":"89271","_id":"37945","publisher":"Royal Society of Chemistry (RSC)","page":"4852-4857","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} }","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.","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>.","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>","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>."}},{"publication":"Ecotoxicology and Environmental Safety","date_created":"2023-01-22T20:23:06Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T4","CSSD"],"type":"journal_article","author":[{"full_name":"Wirth, Marisa A.","last_name":"Wirth","first_name":"Marisa A."},{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"last_name":"Kanwischer","first_name":"Marion","full_name":"Kanwischer, Marion"},{"first_name":"Peter","last_name":"Gros","full_name":"Gros, Peter"},{"first_name":"Peter","last_name":"Leinweber","full_name":"Leinweber, Peter"},{"full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","id":"89271"}],"publication_identifier":{"issn":["0147-6513"]},"year":"2021","title":"AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate","intvolume":"       225","date_updated":"2025-11-10T08:48:20Z","publication_status":"published","language":[{"iso":"eng"}],"article_number":"112768","doi":"10.1016/j.ecoenv.2021.112768","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>"},"status":"public","_id":"37943","publisher":"Elsevier BV","volume":225,"user_id":"89271"},{"issue":"4","publication":"Advanced Synthesis and Catalysis","extern":"1","date_created":"2023-01-22T20:30:29Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","publication_identifier":{"issn":["1615-4150","1615-4169"]},"author":[{"full_name":"Liu, Xin","last_name":"Liu","first_name":"Xin"},{"id":"89271","last_name":"Werner","first_name":"Thomas","orcid":"https://orcid.org/0000-0001-9025-3244","full_name":"Werner, Thomas"}],"year":"2021","title":"Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides","intvolume":"       363","date_updated":"2025-11-10T08:48:47Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1002/adsc.202001209","citation":{"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>.","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} }","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>","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>.","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>","short":"X. Liu, T. Werner, Advanced Synthesis and Catalysis 363 (2021) 1096–1104.","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>."},"status":"public","publisher":"Wiley","_id":"37948","page":"1096-1104","volume":363,"user_id":"89271"},{"citation":{"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>.","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). 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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"},{"citation":{"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>","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>.","short":"X. Liu, J.G. de Vries, T. 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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>","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} }"},"status":"public","volume":21,"user_id":"89271","_id":"37961","publisher":"Royal Society of Chemistry (RSC)","page":"5248-5255","abstract":[{"lang":"eng","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>"}],"extern":"1","publication":"Green Chemistry","issue":"19","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:43:38Z","intvolume":"        21","date_updated":"2025-11-10T08:55:06Z","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"full_name":"Liu, Xin","first_name":"Xin","last_name":"Liu"},{"full_name":"de Vries, Johannes G.","first_name":"Johannes G.","last_name":"de Vries"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"year":"2019","title":"Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts","doi":"10.1039/c9gc02052g","language":[{"iso":"eng"}]},{"doi":"10.1002/cssc.201900678","language":[{"iso":"eng"}],"intvolume":"        12","publication_status":"published","date_updated":"2025-11-10T08:56:56Z","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"full_name":"Kohrt, Christina","first_name":"Christina","last_name":"Kohrt"},{"first_name":"Christoph","last_name":"Wulf","full_name":"Wulf, Christoph"},{"last_name":"Schäffner","first_name":"Benjamin","full_name":"Schäffner, Benjamin"},{"first_name":"Karsten","last_name":"Groenke","full_name":"Groenke, Karsten"},{"last_name":"Hu","first_name":"Yuya","full_name":"Hu, Yuya"},{"full_name":"Kruse, Daniela","first_name":"Daniela","last_name":"Kruse"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"title":"Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate","year":"2019","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T4","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:44:24Z","extern":"1","issue":"12","publication":"ChemSusChem","volume":12,"user_id":"89271","_id":"37963","publisher":"Wiley","page":"2701-2707","status":"public","citation":{"ama":"Büttner H, Kohrt C, Wulf C, et al. 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