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Winter, Nachrichten Aus Der Chemie 69 (2021) 38–68."},"volume":69,"user_id":"89271","_id":"37947","publisher":"Wiley","page":"38-68","status":"public"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1"],"date_created":"2023-01-22T20:34:17Z","extern":"1","issue":"1","publication":"ChemSusChem","doi":"10.1002/cssc.202002267","language":[{"iso":"eng"}],"intvolume":"        14","date_updated":"2025-11-10T08:04:27Z","publication_status":"published","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"full_name":"Wei, Zhihong","first_name":"Zhihong","last_name":"Wei"},{"full_name":"Frey, Anna","last_name":"Frey","first_name":"Anna"},{"full_name":"Kubis, Christoph","last_name":"Kubis","first_name":"Christoph"},{"full_name":"Ren, Chang‐Yue","last_name":"Ren","first_name":"Chang‐Yue"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"last_name":"Jiao","first_name":"Haijun","full_name":"Jiao, Haijun"},{"full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","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","citation":{"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>.","short":"Y. Hu, Z. Wei, A. Frey, C. Kubis, C. Ren, A. Spannenberg, H. Jiao, T. Werner, ChemSusChem 14 (2021) 363–372.","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>","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>.","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>","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} }","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>."},"volume":14,"user_id":"89271","publisher":"Wiley","_id":"37950","page":"363-372","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>"},"volume":53,"user_id":"89271","_id":"37946","publisher":"Georg Thieme Verlag KG","page":"3545-3554","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","T4","CSSD"],"type":"journal_article","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","publication_status":"published","date_updated":"2025-11-10T08:47:47Z","publication_identifier":{"issn":["0039-7881","1437-210X"]},"author":[{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","id":"89271"},{"full_name":"Grandane, Aiga","first_name":"Aiga","last_name":"Grandane"},{"first_name":"Linda","last_name":"Pudnika","full_name":"Pudnika, Linda"},{"last_name":"Domraceva","first_name":"Ilona","full_name":"Domraceva, Ilona"},{"full_name":"Zalubovskis, Raivis","first_name":"Raivis","last_name":"Zalubovskis"}],"title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones","year":"2021"},{"_id":"37944","publisher":"Royal Society of Chemistry (RSC)","page":"10590-10597","volume":12,"user_id":"89271","status":"public","citation":{"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>","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.","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>.","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>"},"language":[{"iso":"eng"}],"doi":"10.1039/d1sc02663a","publication_identifier":{"issn":["2041-6520","2041-6539"]},"author":[{"last_name":"Liu","first_name":"Xin","full_name":"Liu, Xin"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","first_name":"Thomas"}],"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","intvolume":"        12","publication_status":"published","date_updated":"2025-11-10T08:49:01Z","date_created":"2023-01-22T20:24:03Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","issue":"31","publication":"Chemical Science","abstract":[{"lang":"eng","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>"}]},{"citation":{"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>","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."},"status":"public","volume":23,"user_id":"89271","publisher":"Royal Society of Chemistry (RSC)","_id":"37945","page":"4852-4857","abstract":[{"lang":"eng","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>"}],"issue":"13","publication":"Green Chemistry","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"],"date_created":"2023-01-22T20:25:13Z","intvolume":"        23","date_updated":"2025-11-10T08:48:01Z","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"last_name":"Tönjes","first_name":"Jan","full_name":"Tönjes, Jan"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","id":"89271"}],"year":"2021","title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","doi":"10.1039/d1gc00953b","language":[{"iso":"eng"}]},{"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>.","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>","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} }","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>","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>.","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)."},"volume":225,"user_id":"89271","publisher":"Elsevier BV","_id":"37943","status":"public","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","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","author":[{"full_name":"Wirth, Marisa A.","first_name":"Marisa A.","last_name":"Wirth"},{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"first_name":"Marion","last_name":"Kanwischer","full_name":"Kanwischer, Marion"},{"full_name":"Gros, Peter","last_name":"Gros","first_name":"Peter"},{"full_name":"Leinweber, Peter","first_name":"Peter","last_name":"Leinweber"},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244"}],"publication_identifier":{"issn":["0147-6513"]},"year":"2021","title":"AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate"},{"doi":"10.1002/adsc.202001209","language":[{"iso":"eng"}],"publication_status":"published","date_updated":"2025-11-10T08:48:47Z","intvolume":"       363","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":[{"last_name":"Liu","first_name":"Xin","full_name":"Liu, Xin"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","full_name":"Werner, Thomas"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:30:29Z","extern":"1","issue":"4","publication":"Advanced Synthesis and Catalysis","user_id":"89271","volume":363,"page":"1096-1104","publisher":"Wiley","_id":"37948","status":"public","citation":{"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>.","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>.","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>.","ama":"Liu X, Werner T. 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