[{"title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","date_created":"2023-01-22T20:25:13Z","publisher":"Royal Society of Chemistry (RSC)","year":"2021","issue":"13","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"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>"}],"publication":"Green Chemistry","doi":"10.1039/d1gc00953b","author":[{"first_name":"Jan","full_name":"Tönjes, Jan","last_name":"Tönjes"},{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":23,"date_updated":"2025-11-10T08:48:01Z","citation":{"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} }","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>.","short":"J. Tönjes, L. Longwitz, T. Werner, Green Chemistry 23 (2021) 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>","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>."},"page":"4852-4857","intvolume":"        23","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37945","status":"public","type":"journal_article"},{"publication_status":"published","publication_identifier":{"issn":["1083-6160","1520-586X"]},"issue":"1","year":"2021","citation":{"ama":"Stefanow V, Grandane A, Eh M, Panten J, Spannenberg A, Werner T. Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>. 2021;25(1):89-97. doi:<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>","chicago":"Stefanow, Vivian, Aiga Grandane, Marcus Eh, Johannes Panten, Anke Spannenberg, and Thomas Werner. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp; Development</i> 25, no. 1 (2021): 89–97. <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">https://doi.org/10.1021/acs.oprd.0c00423</a>.","ieee":"V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, and T. Werner, “Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant,” <i>Organic Process Research &#38;amp; Development</i>, vol. 25, no. 1, pp. 89–97, 2021, doi: <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>.","mla":"Stefanow, Vivian, et al. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp; Development</i>, vol. 25, no. 1, American Chemical Society (ACS), 2021, pp. 89–97, doi:<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>.","short":"V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, T. Werner, Organic Process Research &#38;amp; Development 25 (2021) 89–97.","bibtex":"@article{Stefanow_Grandane_Eh_Panten_Spannenberg_Werner_2021, title={Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant}, volume={25}, DOI={<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>}, number={1}, journal={Organic Process Research &#38;amp; Development}, publisher={American Chemical Society (ACS)}, author={Stefanow, Vivian and Grandane, Aiga and Eh, Marcus and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2021}, pages={89–97} }","apa":"Stefanow, V., Grandane, A., Eh, M., Panten, J., Spannenberg, A., &#38; Werner, T. (2021). Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>, <i>25</i>(1), 89–97. <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">https://doi.org/10.1021/acs.oprd.0c00423</a>"},"page":"89-97","intvolume":"        25","date_updated":"2025-11-10T08:48:33Z","publisher":"American Chemical Society (ACS)","date_created":"2025-11-05T15:26:05Z","author":[{"first_name":"Vivian","last_name":"Stefanow","full_name":"Stefanow, Vivian"},{"last_name":"Grandane","full_name":"Grandane, Aiga","first_name":"Aiga"},{"first_name":"Marcus","last_name":"Eh","full_name":"Eh, Marcus"},{"first_name":"Johannes","last_name":"Panten","full_name":"Panten, Johannes"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"volume":25,"title":"Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant","doi":"10.1021/acs.oprd.0c00423","type":"journal_article","publication":"Organic Process Research &amp; Development","status":"public","_id":"62098","user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"keyword":["T4","CSSD"],"language":[{"iso":"eng"}]},{"department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","_id":"62099","type":"journal_article","status":"public","volume":25,"author":[{"first_name":"Vivian","last_name":"Stefanow","full_name":"Stefanow, Vivian"},{"last_name":"Grandane","full_name":"Grandane, Aiga","first_name":"Aiga"},{"last_name":"Eh","full_name":"Eh, Marcus","first_name":"Marcus"},{"first_name":"Johannes","last_name":"Panten","full_name":"Panten, Johannes"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_updated":"2025-11-10T08:49:27Z","doi":"10.1021/acs.oprd.0c00423","publication_identifier":{"issn":["1083-6160","1520-586X"]},"publication_status":"published","page":"89-97","intvolume":"        25","citation":{"apa":"Stefanow, V., Grandane, A., Eh, M., Panten, J., Spannenberg, A., &#38; Werner, T. (2021). Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>, <i>25</i>(1), 89–97. <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">https://doi.org/10.1021/acs.oprd.0c00423</a>","short":"V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, T. Werner, Organic Process Research &#38;amp; Development 25 (2021) 89–97.","mla":"Stefanow, Vivian, et al. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp; Development</i>, vol. 25, no. 1, American Chemical Society (ACS), 2021, pp. 89–97, doi:<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>.","bibtex":"@article{Stefanow_Grandane_Eh_Panten_Spannenberg_Werner_2021, title={Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant}, volume={25}, DOI={<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>}, number={1}, journal={Organic Process Research &#38;amp; Development}, publisher={American Chemical Society (ACS)}, author={Stefanow, Vivian and Grandane, Aiga and Eh, Marcus and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2021}, pages={89–97} }","ieee":"V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, and T. Werner, “Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant,” <i>Organic Process Research &#38;amp; Development</i>, vol. 25, no. 1, pp. 89–97, 2021, doi: <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>.","chicago":"Stefanow, Vivian, Aiga Grandane, Marcus Eh, Johannes Panten, Anke Spannenberg, and Thomas Werner. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp; Development</i> 25, no. 1 (2021): 89–97. <a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">https://doi.org/10.1021/acs.oprd.0c00423</a>.","ama":"Stefanow V, Grandane A, Eh M, Panten J, Spannenberg A, Werner T. Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>. 2021;25(1):89-97. doi:<a href=\"https://doi.org/10.1021/acs.oprd.0c00423\">10.1021/acs.oprd.0c00423</a>"},"language":[{"iso":"eng"}],"keyword":["T4","CSSD"],"publication":"Organic Process Research &amp; Development","date_created":"2025-11-05T15:28:23Z","publisher":"American Chemical Society (ACS)","title":"Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant","issue":"1","year":"2021"},{"status":"public","type":"journal_article","publication":"Ecotoxicology and Environmental Safety","article_number":"112768","keyword":["T4","CSSD"],"language":[{"iso":"eng"}],"_id":"37943","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2021","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>.","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>.","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>","short":"M.A. Wirth, L. Longwitz, M. Kanwischer, P. Gros, P. Leinweber, T. Werner, Ecotoxicology and Environmental Safety 225 (2021).","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} }","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>.","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>"},"intvolume":"       225","publication_status":"published","publication_identifier":{"issn":["0147-6513"]},"title":"AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate","doi":"10.1016/j.ecoenv.2021.112768","publisher":"Elsevier BV","date_updated":"2025-11-10T08:48:20Z","date_created":"2023-01-22T20:23:06Z","author":[{"last_name":"Wirth","full_name":"Wirth, Marisa A.","first_name":"Marisa A."},{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"first_name":"Marion","full_name":"Kanwischer, Marion","last_name":"Kanwischer"},{"full_name":"Gros, Peter","last_name":"Gros","first_name":"Peter"},{"first_name":"Peter","full_name":"Leinweber, Peter","last_name":"Leinweber"},{"last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":225},{"_id":"37948","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public","date_updated":"2025-11-10T08:48:47Z","author":[{"last_name":"Liu","full_name":"Liu, Xin","first_name":"Xin"},{"full_name":"Werner, Thomas","id":"89271","orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":363,"doi":"10.1002/adsc.202001209","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"citation":{"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>.","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>.","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>","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>.","short":"X. Liu, T. Werner, Advanced Synthesis and Catalysis 363 (2021) 1096–1104.","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} }","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>"},"page":"1096-1104","intvolume":"       363","keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"publication":"Advanced Synthesis and Catalysis","publisher":"Wiley","date_created":"2023-01-22T20:30:29Z","title":"Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides","issue":"4","year":"2021"},{"type":"journal_article","publication":"Angewandte Chemie","status":"public","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The carbon–carbon double bond of unsaturated carbonyl compounds was readily reduced by using a phosphetane oxide catalyst in the presence of a simple organosilane as the terminal reductant and water as the hydrogen source. Quantitative hydrogenation was observed when 1.0 mol % of a methyl‐substituted phosphetane oxide was employed as the catalyst. The procedure is highly selective towards activated double bonds, tolerating a variety of functional groups that are usually prone to reduction. In total, 25 alkenes and two alkynes were hydrogenated to the corresponding alkanes in excellent yields of up to 99 %. Notably, less active poly(methylhydrosiloxane) could also be utilized as the terminal reductant. Mechanistic investigations revealed the phosphane as the catalyst resting state and a protonation/deprotonation sequence as the crucial step in the catalytic cycle.</jats:p>","lang":"eng"}],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62101","language":[{"iso":"eng"}],"keyword":["T2","T4"],"issue":"7","publication_status":"published","publication_identifier":{"issn":["0044-8249","1521-3757"]},"citation":{"short":"L. Longwitz, T. Werner, Angewandte Chemie 132 (2020) 2782–2785.","bibtex":"@article{Longwitz_Werner_2020, title={Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis}, volume={132}, DOI={<a href=\"https://doi.org/10.1002/ange.201912991\">10.1002/ange.201912991</a>}, number={7}, journal={Angewandte Chemie}, publisher={Wiley}, author={Longwitz, Lars and Werner, Thomas}, year={2020}, pages={2782–2785} }","mla":"Longwitz, Lars, and Thomas Werner. “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis.” <i>Angewandte Chemie</i>, vol. 132, no. 7, Wiley, 2020, pp. 2782–85, doi:<a href=\"https://doi.org/10.1002/ange.201912991\">10.1002/ange.201912991</a>.","apa":"Longwitz, L., &#38; Werner, T. (2020). Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis. <i>Angewandte Chemie</i>, <i>132</i>(7), 2782–2785. <a href=\"https://doi.org/10.1002/ange.201912991\">https://doi.org/10.1002/ange.201912991</a>","ama":"Longwitz L, Werner T. Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis. <i>Angewandte Chemie</i>. 2020;132(7):2782-2785. doi:<a href=\"https://doi.org/10.1002/ange.201912991\">10.1002/ange.201912991</a>","chicago":"Longwitz, Lars, and Thomas Werner. “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis.” <i>Angewandte Chemie</i> 132, no. 7 (2020): 2782–85. <a href=\"https://doi.org/10.1002/ange.201912991\">https://doi.org/10.1002/ange.201912991</a>.","ieee":"L. Longwitz and T. Werner, “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis,” <i>Angewandte Chemie</i>, vol. 132, no. 7, pp. 2782–2785, 2020, doi: <a href=\"https://doi.org/10.1002/ange.201912991\">10.1002/ange.201912991</a>."},"intvolume":"       132","page":"2782-2785","year":"2020","date_created":"2025-11-05T15:39:06Z","author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":132,"date_updated":"2025-11-10T08:11:23Z","publisher":"Wiley","doi":"10.1002/ange.201912991","title":"Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis"},{"citation":{"bibtex":"@article{Werner_Stefanow_Grandane_Panten_Eh_2020, title={Novel processes for preparing cis-cedrandiol}, author={Werner, Thomas and Stefanow, V. and Grandane, A. and Panten, J. and Eh, M.}, year={2020} }","short":"T. Werner, V. Stefanow, A. Grandane, J. Panten, M. Eh, (2020).","mla":"Werner, Thomas, et al. <i>Novel Processes for Preparing Cis-Cedrandiol</i>. 2020.","apa":"Werner, T., Stefanow, V., Grandane, A., Panten, J., &#38; Eh, M. (2020). <i>Novel processes for preparing cis-cedrandiol</i>.","ama":"Werner T, Stefanow V, Grandane A, Panten J, Eh M. Novel processes for preparing cis-cedrandiol. Published online 2020.","chicago":"Werner, Thomas, V. Stefanow, A. Grandane, J. Panten, and M. Eh. “Novel Processes for Preparing Cis-Cedrandiol,” 2020.","ieee":"T. Werner, V. Stefanow, A. Grandane, J. Panten, and M. 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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.","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>","ama":"Andexer JN, Beifuss U, Beuerle F, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2020;68(3):42-72. doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">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>.","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>."},"volume":68,"author":[{"last_name":"Andexer","full_name":"Andexer, Jennifer N.","first_name":"Jennifer N."},{"first_name":"Uwe","last_name":"Beifuss","full_name":"Beifuss, Uwe"},{"last_name":"Beuerle","full_name":"Beuerle, Florian","first_name":"Florian"},{"first_name":"Malte","full_name":"Brasholz, Malte","last_name":"Brasholz"},{"last_name":"Breinbauer","full_name":"Breinbauer, Rolf","first_name":"Rolf"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"first_name":"Julian","full_name":"Greb, Julian","last_name":"Greb"},{"full_name":"Gulder, Tobias","last_name":"Gulder","first_name":"Tobias"},{"last_name":"Hüttel","full_name":"Hüttel, Wolfgang","first_name":"Wolfgang"},{"first_name":"Stephanie","full_name":"Kath‐Schorr, Stephanie","last_name":"Kath‐Schorr"},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"last_name":"Lehmann","full_name":"Lehmann, Matthias","first_name":"Matthias"},{"first_name":"Thomas","last_name":"Lindel","full_name":"Lindel, Thomas"},{"last_name":"Luy","full_name":"Luy, Burkhard","first_name":"Burkhard"},{"last_name":"Mück‐Lichtenfeld","full_name":"Mück‐Lichtenfeld, Christian","first_name":"Christian"},{"first_name":"Claudia","full_name":"Muhle, Claudia","last_name":"Muhle"},{"first_name":"Arun","last_name":"Narine","full_name":"Narine, Arun"},{"first_name":"Jörg","last_name":"Niemeyer","full_name":"Niemeyer, Jörg"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan","first_name":"Jan"},{"first_name":"Roland","full_name":"Pfau, Roland","last_name":"Pfau"},{"full_name":"Pietruszka, Jörg","last_name":"Pietruszka","first_name":"Jörg"},{"full_name":"Schaschke, Norbert","last_name":"Schaschke","first_name":"Norbert"},{"last_name":"Senge","full_name":"Senge, Mathias","first_name":"Mathias"},{"first_name":"Bernd F.","last_name":"Straub","full_name":"Straub, Bernd F."},{"last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"last_name":"Winter","full_name":"Winter, Christian","first_name":"Christian"}],"date_updated":"2025-11-10T08:13:43Z","doi":"10.1002/nadc.20204095515"},{"_id":"62102","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","keyword":["T2","T4","CSSD"],"language":[{"iso":"eng"}],"publication":"Angewandte Chemie International Edition","type":"journal_article","abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>The carbon–carbon double bond of unsaturated carbonyl compounds was readily reduced by using a phosphetane oxide catalyst in the presence of a simple organosilane as the terminal reductant and water as the hydrogen source. Quantitative hydrogenation was observed when 1.0 mol % of a methyl‐substituted phosphetane oxide was employed as the catalyst. The procedure is highly selective towards activated double bonds, tolerating a variety of functional groups that are usually prone to reduction. In total, 25 alkenes and two alkynes were hydrogenated to the corresponding alkanes in excellent yields of up to 99 %. Notably, less active poly(methylhydrosiloxane) could also be utilized as the terminal reductant. Mechanistic investigations revealed the phosphane as the catalyst resting state and a protonation/deprotonation sequence as the crucial step in the catalytic cycle.</jats:p>","lang":"eng"}],"status":"public","publisher":"Wiley","date_updated":"2025-11-10T08:49:52Z","volume":59,"date_created":"2025-11-05T15:39:56Z","author":[{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas"}],"title":"Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis","doi":"10.1002/anie.201912991","publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","issue":"7","year":"2020","page":"2760-2763","intvolume":"        59","citation":{"ama":"Longwitz L, Werner T. Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis. <i>Angewandte Chemie International Edition</i>. 2020;59(7):2760-2763. doi:<a href=\"https://doi.org/10.1002/anie.201912991\">10.1002/anie.201912991</a>","ieee":"L. Longwitz and T. Werner, “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis,” <i>Angewandte Chemie International Edition</i>, vol. 59, no. 7, pp. 2760–2763, 2020, doi: <a href=\"https://doi.org/10.1002/anie.201912991\">10.1002/anie.201912991</a>.","chicago":"Longwitz, Lars, and Thomas Werner. “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis.” <i>Angewandte Chemie International Edition</i> 59, no. 7 (2020): 2760–63. <a href=\"https://doi.org/10.1002/anie.201912991\">https://doi.org/10.1002/anie.201912991</a>.","mla":"Longwitz, Lars, and Thomas Werner. “Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis.” <i>Angewandte Chemie International Edition</i>, vol. 59, no. 7, Wiley, 2020, pp. 2760–63, doi:<a href=\"https://doi.org/10.1002/anie.201912991\">10.1002/anie.201912991</a>.","short":"L. Longwitz, T. Werner, Angewandte Chemie International Edition 59 (2020) 2760–2763.","bibtex":"@article{Longwitz_Werner_2020, title={Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis}, volume={59}, DOI={<a href=\"https://doi.org/10.1002/anie.201912991\">10.1002/anie.201912991</a>}, number={7}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Longwitz, Lars and Werner, Thomas}, year={2020}, pages={2760–2763} }","apa":"Longwitz, L., &#38; Werner, T. (2020). Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis. <i>Angewandte Chemie International Edition</i>, <i>59</i>(7), 2760–2763. <a href=\"https://doi.org/10.1002/anie.201912991\">https://doi.org/10.1002/anie.201912991</a>"}},{"keyword":["T3","CSSD"],"language":[{"iso":"eng"}],"publication":"ACS Catalysis","title":"Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:35:25Z","year":"2020","issue":"22","extern":"1","_id":"37951","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","status":"public","type":"journal_article","doi":"10.1021/acscatal.0c03294","date_updated":"2025-11-10T08:50:10Z","volume":10,"author":[{"full_name":"Liu, Xin","last_name":"Liu","first_name":"Xin"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"last_name":"Spiegelberg","full_name":"Spiegelberg, Brian","first_name":"Brian"},{"full_name":"Tönjes, Jan","last_name":"Tönjes","first_name":"Jan"},{"first_name":"Torsten","full_name":"Beweries, Torsten","last_name":"Beweries"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"intvolume":"        10","page":"13659-13667","citation":{"bibtex":"@article{Liu_Longwitz_Spiegelberg_Tönjes_Beweries_Werner_2020, title={Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions}, volume={10}, DOI={<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>}, number={22}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Liu, Xin and Longwitz, Lars and Spiegelberg, Brian and Tönjes, Jan and Beweries, Torsten and Werner, Thomas}, year={2020}, pages={13659–13667} }","mla":"Liu, Xin, et al. “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions.” <i>ACS Catalysis</i>, vol. 10, no. 22, American Chemical Society (ACS), 2020, pp. 13659–67, doi:<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>.","short":"X. Liu, L. Longwitz, B. Spiegelberg, J. Tönjes, T. Beweries, T. Werner, ACS Catalysis 10 (2020) 13659–13667.","apa":"Liu, X., Longwitz, L., Spiegelberg, B., Tönjes, J., Beweries, T., &#38; Werner, T. (2020). Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions. <i>ACS Catalysis</i>, <i>10</i>(22), 13659–13667. <a href=\"https://doi.org/10.1021/acscatal.0c03294\">https://doi.org/10.1021/acscatal.0c03294</a>","ama":"Liu X, Longwitz L, Spiegelberg B, Tönjes J, Beweries T, Werner T. Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions. <i>ACS Catalysis</i>. 2020;10(22):13659-13667. doi:<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>","chicago":"Liu, Xin, Lars Longwitz, Brian Spiegelberg, Jan Tönjes, Torsten Beweries, and Thomas Werner. “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions.” <i>ACS Catalysis</i> 10, no. 22 (2020): 13659–67. <a href=\"https://doi.org/10.1021/acscatal.0c03294\">https://doi.org/10.1021/acscatal.0c03294</a>.","ieee":"X. Liu, L. Longwitz, B. Spiegelberg, J. Tönjes, T. Beweries, and T. Werner, “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions,” <i>ACS Catalysis</i>, vol. 10, no. 22, pp. 13659–13667, 2020, doi: <a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>."},"publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published"},{"publication":"ACS Sustainable Chemistry and Engineering","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37955","language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T3","CSSD"],"issue":"3","publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","intvolume":"         8","page":"1651-1658","citation":{"ieee":"C. Wulf, M. Reckers, A. Perechodjuk, and T. Werner, “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 8, no. 3, pp. 1651–1658, 2020, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>.","chicago":"Wulf, Christoph, Matthias Reckers, Anna Perechodjuk, and Thomas Werner. “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes.” <i>ACS Sustainable Chemistry and Engineering</i> 8, no. 3 (2020): 1651–58. <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">https://doi.org/10.1021/acssuschemeng.9b06662</a>.","ama":"Wulf C, Reckers M, Perechodjuk A, Werner T. Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes. <i>ACS Sustainable Chemistry and Engineering</i>. 2020;8(3):1651-1658. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>","short":"C. Wulf, M. Reckers, A. Perechodjuk, T. Werner, ACS Sustainable Chemistry and Engineering 8 (2020) 1651–1658.","mla":"Wulf, Christoph, et al. “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 8, no. 3, American Chemical Society (ACS), 2020, pp. 1651–58, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>.","bibtex":"@article{Wulf_Reckers_Perechodjuk_Werner_2020, title={Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes}, volume={8}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>}, number={3}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Wulf, Christoph and Reckers, Matthias and Perechodjuk, Anna and Werner, Thomas}, year={2020}, pages={1651–1658} }","apa":"Wulf, C., Reckers, M., Perechodjuk, A., &#38; Werner, T. (2020). Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes. <i>ACS Sustainable Chemistry and Engineering</i>, <i>8</i>(3), 1651–1658. <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">https://doi.org/10.1021/acssuschemeng.9b06662</a>"},"year":"2020","volume":8,"date_created":"2023-01-22T20:39:32Z","author":[{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"full_name":"Reckers, Matthias","last_name":"Reckers","first_name":"Matthias"},{"last_name":"Perechodjuk","full_name":"Perechodjuk, Anna","first_name":"Anna"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:51:03Z","doi":"10.1021/acssuschemeng.9b06662","title":"Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes"},{"doi":"10.1002/cssc.201903384","volume":13,"author":[{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"first_name":"Sandra","last_name":"Peglow","full_name":"Peglow, Sandra"},{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Marcus","last_name":"Frank","full_name":"Frank, Marcus"},{"last_name":"Epping","full_name":"Epping, Jan Dirk","first_name":"Jan Dirk"},{"first_name":"Volker","full_name":"Brüser, Volker","last_name":"Brüser"},{"full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"date_updated":"2025-11-10T08:50:25Z","page":"1825-1833","intvolume":"        13","citation":{"chicago":"Hu, Yuya, Sandra Peglow, Lars Longwitz, Marcus Frank, Jan Dirk Epping, Volker Brüser, and Thomas Werner. “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>.” <i>ChemSusChem</i> 13, no. 7 (2020): 1825–33. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>.","ieee":"Y. Hu <i>et al.</i>, “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>,” <i>ChemSusChem</i>, vol. 13, no. 7, pp. 1825–1833, 2020, doi: <a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>.","ama":"Hu Y, Peglow S, Longwitz L, et al. Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>. 2020;13(7):1825-1833. doi:<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>","apa":"Hu, Y., Peglow, S., Longwitz, L., Frank, M., Epping, J. D., Brüser, V., &#38; Werner, T. (2020). Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>, <i>13</i>(7), 1825–1833. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>","short":"Y. Hu, S. Peglow, L. Longwitz, M. Frank, J.D. Epping, V. Brüser, T. 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(2019). Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature. <i>ACS Catalysis</i>, <i>9</i>(10), 9237–9244. <a href=\"https://doi.org/10.1021/acscatal.9b02456\">https://doi.org/10.1021/acscatal.9b02456</a>","mla":"Longwitz, Lars, et al. “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature.” <i>ACS Catalysis</i>, vol. 9, no. 10, American Chemical Society (ACS), 2019, pp. 9237–44, doi:<a href=\"https://doi.org/10.1021/acscatal.9b02456\">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} }","short":"L. 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Werner, “Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature,” <i>ACS Catalysis</i>, vol. 9, no. 10, pp. 9237–9244, 2019, doi: <a href=\"https://doi.org/10.1021/acscatal.9b02456\">10.1021/acscatal.9b02456</a>."},"publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published"},{"publisher":"Wiley","date_created":"2023-01-22T20:44:46Z","title":"Trendbericht Organische Chemie","issue":"3","year":"2019","keyword":["General Chemical Engineering","General Chemistry"],"language":[{"iso":"eng"}],"publication":"Nachrichten aus der Chemie","date_updated":"2025-11-10T08:57:09Z","author":[{"last_name":"Andexer","full_name":"Andexer, Jennifer N.","first_name":"Jennifer N."},{"full_name":"Beifuss, Uwe","last_name":"Beifuss","first_name":"Uwe"},{"first_name":"Florian","full_name":"Beuerle, Florian","last_name":"Beuerle"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"last_name":"Ernst","full_name":"Ernst, Martin","first_name":"Martin"},{"last_name":"Gulder","full_name":"Gulder, Tobias A. 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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>.","chicago":"Hu, Yuya, Johannes Steinbauer, Vivian Stefanow, Anke Spannenberg, and Thomas Werner. “Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ACS Sustainable Chemistry and Engineering</i> 7, no. 15 (2019): 13257–69. <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">https://doi.org/10.1021/acssuschemeng.9b02502</a>.","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>","short":"Y. Hu, J. Steinbauer, V. Stefanow, A. Spannenberg, T. Werner, ACS Sustainable Chemistry and Engineering 7 (2019) 13257–13269.","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} }","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>.","apa":"Hu, Y., Steinbauer, J., Stefanow, V., Spannenberg, A., &#38; Werner, T. (2019). Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ACS Sustainable Chemistry and Engineering</i>, <i>7</i>(15), 13257–13269. <a href=\"https://doi.org/10.1021/acssuschemeng.9b02502\">https://doi.org/10.1021/acssuschemeng.9b02502</a>"},"publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","extern":"1","_id":"37957","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","status":"public","type":"journal_article"},{"publication_identifier":{"issn":["0022-3263","1520-6904"]},"publication_status":"published","issue":"12","year":"2019","page":"7863-7870","intvolume":"        84","citation":{"ama":"Longwitz L, Jopp S, Werner T. Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. <i>The Journal of Organic Chemistry</i>. 2019;84(12):7863-7870. doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>","ieee":"L. Longwitz, S. Jopp, and T. 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Werner, The Journal of Organic Chemistry 84 (2019) 7863–7870.","bibtex":"@article{Longwitz_Jopp_Werner_2019, title={Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling}, volume={84}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>}, number={12}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Jopp, Stefan and Werner, Thomas}, year={2019}, pages={7863–7870} }","mla":"Longwitz, Lars, et al. “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling.” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 12, American Chemical Society (ACS), 2019, pp. 7863–70, doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>."},"publisher":"American Chemical Society (ACS)","date_updated":"2025-11-10T08:54:28Z","volume":84,"date_created":"2023-01-22T20:44:02Z","author":[{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Jopp, Stefan","last_name":"Jopp","first_name":"Stefan"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"title":"Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling","doi":"10.1021/acs.joc.9b00741","publication":"The Journal of Organic Chemistry","type":"journal_article","status":"public","_id":"37962","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["T2","CSSD"],"extern":"1","language":[{"iso":"eng"}]},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37959","type":"journal_article","status":"public","volume":365,"author":[{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"date_updated":"2025-11-10T09:01:38Z","doi":"10.1126/science.aay6635","publication_identifier":{"issn":["0036-8075","1095-9203"]},"publication_status":"published","page":"866-867","intvolume":"       365","citation":{"ama":"Longwitz L, Werner T. 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The Mitsunobu reaction, reimagined. <i>Science</i>, <i>365</i>(6456), 866–867. <a href=\"https://doi.org/10.1126/science.aay6635\">https://doi.org/10.1126/science.aay6635</a>"},"language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"publication":"Science","abstract":[{"lang":"eng","text":"<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>"}],"date_created":"2023-01-22T20:42:20Z","publisher":"American Association for the Advancement of Science (AAAS)","title":"The Mitsunobu reaction, reimagined","issue":"6456","year":"2019"}]