[{"doi":"10.1039/d3gc03993e","title":"Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines","date_created":"2025-11-05T15:16:32Z","author":[{"first_name":"Changyue","last_name":"Ren","full_name":"Ren, Changyue"},{"first_name":"Constanza","last_name":"Terazzi","full_name":"Terazzi, Constanza"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":26,"publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T08:44:44Z","citation":{"short":"C. Ren, C. Terazzi, T. Werner, Green Chemistry 26 (2024) 439–447.","mla":"Ren, Changyue, et al. “Tuneable Reduction of CO<sub>2</sub> – Organocatalyzed Selective Formylation and Methylation of Amines.” <i>Green Chemistry</i>, vol. 26, no. 1, Royal Society of Chemistry (RSC), 2024, pp. 439–47, doi:<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>.","bibtex":"@article{Ren_Terazzi_Werner_2024, title={Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines}, volume={26}, DOI={<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>}, number={1}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Ren, Changyue and Terazzi, Constanza and Werner, Thomas}, year={2024}, pages={439–447} }","apa":"Ren, C., Terazzi, C., &#38; Werner, T. (2024). Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines. <i>Green Chemistry</i>, <i>26</i>(1), 439–447. <a href=\"https://doi.org/10.1039/d3gc03993e\">https://doi.org/10.1039/d3gc03993e</a>","ama":"Ren C, Terazzi C, Werner T. Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines. <i>Green Chemistry</i>. 2024;26(1):439-447. doi:<a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>","chicago":"Ren, Changyue, Constanza Terazzi, and Thomas Werner. “Tuneable Reduction of CO<sub>2</sub> – Organocatalyzed Selective Formylation and Methylation of Amines.” <i>Green Chemistry</i> 26, no. 1 (2024): 439–47. <a href=\"https://doi.org/10.1039/d3gc03993e\">https://doi.org/10.1039/d3gc03993e</a>.","ieee":"C. Ren, C. Terazzi, and T. Werner, “Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines,” <i>Green Chemistry</i>, vol. 26, no. 1, pp. 439–447, 2024, doi: <a href=\"https://doi.org/10.1039/d3gc03993e\">10.1039/d3gc03993e</a>."},"intvolume":"        26","page":"439-447","year":"2024","issue":"1","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"language":[{"iso":"eng"}],"keyword":["T1","T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"}],"_id":"62090","status":"public","abstract":[{"text":"<jats:p>The selective <jats:italic>N</jats:italic>-formylation and <jats:italic>N</jats:italic>-methylation of amines with carbon dioxide (CO<jats:sub>2</jats:sub>) catalyzed by methyltriphenylphosphonium methylcarbonate and tuned by polymethylhydrosiloxane or trimethoxysilane as reducing agents is reported.</jats:p>","lang":"eng"}],"type":"journal_article","publication":"Green Chemistry"},{"doi":"10.1039/d1gc00953b","date_updated":"2025-11-10T08:48:01Z","author":[{"full_name":"Tönjes, Jan","last_name":"Tönjes","first_name":"Jan"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":23,"citation":{"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>.","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>","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>","short":"J. Tönjes, L. Longwitz, T. Werner, Green Chemistry 23 (2021) 4852–4857.","bibtex":"@article{Tönjes_Longwitz_Werner_2021, title={Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction}, volume={23}, DOI={<a href=\"https://doi.org/10.1039/d1gc00953b\">10.1039/d1gc00953b</a>}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tönjes, Jan and Longwitz, Lars and Werner, Thomas}, year={2021}, pages={4852–4857} }","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>."},"intvolume":"        23","page":"4852-4857","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"_id":"37945","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article","title":"Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T20:25:13Z","year":"2021","issue":"13","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"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"}],"publication":"Green Chemistry"},{"issue":"19","year":"2019","date_created":"2023-01-22T20:43:38Z","publisher":"Royal Society of Chemistry (RSC)","title":"Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts","publication":"Green Chemistry","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>"}],"language":[{"iso":"eng"}],"keyword":["T3","CSSD"],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","intvolume":"        21","page":"5248-5255","citation":{"chicago":"Liu, Xin, Johannes G. de Vries, and Thomas Werner. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i> 21, no. 19 (2019): 5248–55. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>.","ieee":"X. Liu, J. G. de Vries, and T. Werner, “Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts,” <i>Green Chemistry</i>, vol. 21, no. 19, pp. 5248–5255, 2019, doi: <a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","ama":"Liu X, de Vries JG, Werner T. Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>. 2019;21(19):5248-5255. doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>","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>","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} }","short":"X. Liu, J.G. de Vries, T. Werner, Green Chemistry 21 (2019) 5248–5255.","mla":"Liu, Xin, et al. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i>, vol. 21, no. 19, Royal Society of Chemistry (RSC), 2019, pp. 5248–55, doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>."},"volume":21,"author":[{"first_name":"Xin","last_name":"Liu","full_name":"Liu, Xin"},{"first_name":"Johannes G.","last_name":"de Vries","full_name":"de Vries, Johannes G."},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"date_updated":"2025-11-10T08:55:06Z","doi":"10.1039/c9gc02052g","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37961","extern":"1"},{"status":"public","abstract":[{"text":"<p>An immobilized bifunctional phosphonium salt catalyst efficiently catalyzed the synthesis of cyclic carbonates under mild conditions, and was reused up to 15 times.</p>","lang":"eng"}],"publication":"Green Chemistry","type":"journal_article","language":[{"iso":"eng"}],"extern":"1","keyword":["T1","T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37973","intvolume":"        19","page":"4435-4445","citation":{"ieee":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, and T. Werner, “Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides,” <i>Green Chemistry</i>, vol. 19, no. 18, pp. 4435–4445, 2017, doi: <a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>.","chicago":"Steinbauer, J., L. Longwitz, M. Frank, J. Epping, U. Kragl, and Thomas Werner. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i> 19, no. 18 (2017): 4435–45. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>.","ama":"Steinbauer J, Longwitz L, Frank M, Epping J, Kragl U, Werner T. Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>. 2017;19(18):4435-4445. doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>","mla":"Steinbauer, J., et al. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 18, Royal Society of Chemistry (RSC), 2017, pp. 4435–45, doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>.","bibtex":"@article{Steinbauer_Longwitz_Frank_Epping_Kragl_Werner_2017, title={Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>}, number={18}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Longwitz, L. and Frank, M. and Epping, J. and Kragl, U. and Werner, Thomas}, year={2017}, pages={4435–4445} }","short":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 4435–4445.","apa":"Steinbauer, J., Longwitz, L., Frank, M., Epping, J., Kragl, U., &#38; Werner, T. (2017). Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>, <i>19</i>(18), 4435–4445. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>"},"year":"2017","issue":"18","publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published","doi":"10.1039/c7gc01782k","title":"Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides","volume":19,"date_created":"2023-01-22T20:57:38Z","author":[{"full_name":"Steinbauer, J.","last_name":"Steinbauer","first_name":"J."},{"full_name":"Longwitz, L.","last_name":"Longwitz","first_name":"L."},{"first_name":"M.","last_name":"Frank","full_name":"Frank, M."},{"first_name":"J.","full_name":"Epping, J.","last_name":"Epping"},{"first_name":"U.","last_name":"Kragl","full_name":"Kragl, U."},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T09:18:10Z"},{"type":"journal_article","publication":"Green Chemistry","abstract":[{"lang":"eng","text":"<p>Calcium punched beyond its weight: An <italic>in situ</italic> formed Ca<sup>2+</sup>–crown ether complex showed unprecedented efficiency in cyclic carbonate synthesis.</p>"}],"status":"public","_id":"37975","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"extern":"1","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"issue":"16","year":"2017","citation":{"chicago":"Steinbauer, J., A. Spannenberg, and Thomas Werner. “An in Situ Formed Ca<sup>2+</sup>–Crown Ether Complex and Its Use in CO<sub>2</sub>-Fixation Reactions with Terminal and Internal Epoxides.” <i>Green Chemistry</i> 19, no. 16 (2017): 3769–79. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>.","ieee":"J. Steinbauer, A. Spannenberg, and T. Werner, “An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides,” <i>Green Chemistry</i>, vol. 19, no. 16, pp. 3769–3779, 2017, doi: <a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>.","ama":"Steinbauer J, Spannenberg A, Werner T. An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides. <i>Green Chemistry</i>. 2017;19(16):3769-3779. doi:<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>","apa":"Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides. <i>Green Chemistry</i>, <i>19</i>(16), 3769–3779. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>","mla":"Steinbauer, J., et al. “An in Situ Formed Ca<sup>2+</sup>–Crown Ether Complex and Its Use in CO<sub>2</sub>-Fixation Reactions with Terminal and Internal Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 16, Royal Society of Chemistry (RSC), 2017, pp. 3769–79, doi:<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>.","bibtex":"@article{Steinbauer_Spannenberg_Werner_2017, title={An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>}, number={16}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Spannenberg, A. and Werner, Thomas}, year={2017}, pages={3769–3779} }","short":"J. Steinbauer, A. Spannenberg, T. Werner, Green Chemistry 19 (2017) 3769–3779."},"intvolume":"        19","page":"3769-3779","publisher":"Royal Society of Chemistry (RSC)","date_updated":"2025-11-10T09:18:18Z","author":[{"full_name":"Steinbauer, J.","last_name":"Steinbauer","first_name":"J."},{"first_name":"A.","full_name":"Spannenberg, A.","last_name":"Spannenberg"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_created":"2023-01-22T20:59:12Z","volume":19,"title":"An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides","doi":"10.1039/c7gc01114h"},{"keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"<p><bold>Taking Control!</bold>The binary catalyst system composed of MoO<sub>3</sub>and an organic phoshponium salt [Bu<sub>4</sub>P]X proved very efficient to produce oleochemical cyclic carbonates from renewables.</p>"}],"publication":"Green Chemistry","title":"Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T21:03:02Z","year":"2016","issue":"13","extern":"1","_id":"37983","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","status":"public","type":"journal_article","doi":"10.1039/c6gc00671j","date_updated":"2025-11-10T09:20:35Z","volume":18,"author":[{"first_name":"Nils","last_name":"Tenhumberg","full_name":"Tenhumberg, Nils"},{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"first_name":"Benjamin","full_name":"Schäffner, Benjamin","last_name":"Schäffner"},{"first_name":"Daniela","full_name":"Kruse, Daniela","last_name":"Kruse"},{"last_name":"Blumenstein","full_name":"Blumenstein, Michael","first_name":"Michael"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"page":"3775-3788","intvolume":"        18","citation":{"apa":"Tenhumberg, N., Büttner, H., Schäffner, B., Kruse, D., Blumenstein, M., &#38; Werner, T. (2016). Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>, <i>18</i>(13), 3775–3788. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>","bibtex":"@article{Tenhumberg_Büttner_Schäffner_Kruse_Blumenstein_Werner_2016, title={Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables}, volume={18}, DOI={<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}, year={2016}, pages={3775–3788} }","short":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, T. Werner, Green Chemistry 18 (2016) 3775–3788.","mla":"Tenhumberg, Nils, et al. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i>, vol. 18, no. 13, Royal Society of Chemistry (RSC), 2016, pp. 3775–88, doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","chicago":"Tenhumberg, Nils, Hendrik Büttner, Benjamin Schäffner, Daniela Kruse, Michael Blumenstein, and Thomas Werner. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i> 18, no. 13 (2016): 3775–88. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>.","ieee":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, and T. Werner, “Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables,” <i>Green Chemistry</i>, vol. 18, no. 13, pp. 3775–3788, 2016, doi: <a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","ama":"Tenhumberg N, Büttner H, Schäffner B, Kruse D, Blumenstein M, Werner T. Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>. 2016;18(13):3775-3788. doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>"},"publication_identifier":{"issn":["1463-9262","1463-9270"]},"publication_status":"published"}]