[{"citation":{"apa":"Stefanow, V., Kell, L., Leduskrasta, A., Eh, M., Panten, J., &#38; Werner, T. (2025). Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>, <i>90</i>(37), 12877–12887. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>","ieee":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, and T. Werner, “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients,” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, pp. 12877–12887, 2025, doi: <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","chicago":"Stefanow, Vivian, Lukas Kell, Aiga Leduskrasta, Marcus Eh, Johannes Panten, and Thomas Werner. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i> 90, no. 37 (2025): 12877–87. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>.","short":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, T. Werner, The Journal of Organic Chemistry 90 (2025) 12877–12887.","mla":"Stefanow, Vivian, et al. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, American Chemical Society (ACS), 2025, pp. 12877–87, doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","ama":"Stefanow V, Kell L, Leduskrasta A, Eh M, Panten J, Werner T. Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>. 2025;90(37):12877-12887. doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>","bibtex":"@article{Stefanow_Kell_Leduskrasta_Eh_Panten_Werner_2025, title={Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients}, volume={90}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>}, number={37}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Stefanow, Vivian and Kell, Lukas and Leduskrasta, Aiga and Eh, Marcus and Panten, Johannes and Werner, Thomas}, year={2025}, pages={12877–12887} }"},"status":"public","page":"12877-12887","_id":"62086","publisher":"American Chemical Society (ACS)","user_id":"89271","volume":90,"issue":"37","publication":"The Journal of Organic Chemistry","date_created":"2025-11-05T15:10:13Z","type":"journal_article","keyword":["T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"}],"year":"2025","title":"Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients","publication_identifier":{"issn":["0022-3263","1520-6904"]},"author":[{"first_name":"Vivian","last_name":"Stefanow","full_name":"Stefanow, Vivian"},{"full_name":"Kell, Lukas","last_name":"Kell","first_name":"Lukas"},{"full_name":"Leduskrasta, Aiga","first_name":"Aiga","last_name":"Leduskrasta"},{"first_name":"Marcus","last_name":"Eh","full_name":"Eh, Marcus"},{"last_name":"Panten","first_name":"Johannes","full_name":"Panten, Johannes"},{"orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"publication_status":"published","date_updated":"2025-11-10T08:43:33Z","intvolume":"        90","language":[{"iso":"eng"}],"doi":"10.1021/acs.joc.5c00889"},{"doi":"10.1016/j.phytol.2024.06.004","language":[{"iso":"eng"}],"intvolume":"        62","publication_status":"published","date_updated":"2025-11-10T07:45:58Z","author":[{"first_name":"Suzanne L.","last_name":"Nyemeck","full_name":"Nyemeck, Suzanne L."},{"full_name":"Eyong, Kenneth O.","first_name":"Kenneth O.","last_name":"Eyong"},{"last_name":"Bidingha","first_name":"Ronald","full_name":"Bidingha, Ronald"},{"full_name":"Kamdem, Michael HK.","last_name":"Kamdem","first_name":"Michael HK."},{"first_name":"Derek T.","last_name":"Ndinteh","full_name":"Ndinteh, Derek T."},{"last_name":"Odumosu","first_name":"Patricia O.","full_name":"Odumosu, Patricia O."},{"full_name":"Folefoc, Gabriel N.","last_name":"Folefoc","first_name":"Gabriel N."},{"last_name":"Bilanda","first_name":"Danielle C.","full_name":"Bilanda, Danielle C."},{"full_name":"Egbe, Andrew E.","first_name":"Andrew E.","last_name":"Egbe"},{"full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271"},{"full_name":"Bekono, Boris D.","first_name":"Boris D.","last_name":"Bekono"},{"first_name":"Fidele","last_name":"Ntie-Kang","full_name":"Ntie-Kang, Fidele"}],"publication_identifier":{"issn":["1874-3900"]},"title":"Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors","year":"2024","department":[{"_id":"35"},{"_id":"2"}],"keyword":["T4"],"type":"journal_article","date_created":"2025-11-05T15:18:32Z","publication":"Phytochemistry Letters","volume":62,"user_id":"89271","publisher":"Elsevier BV","_id":"62092","page":"59-67","status":"public","citation":{"mla":"Nyemeck, Suzanne L., et al. “Design, Isolation, Synthesis, and Mechanistic Insight of Flavonoids Isolated from Beilschmiedia Obscura, as Potential α-Glucosidase Inhibitors.” <i>Phytochemistry Letters</i>, vol. 62, Elsevier BV, 2024, pp. 59–67, doi:<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>.","bibtex":"@article{Nyemeck_Eyong_Bidingha_Kamdem_Ndinteh_Odumosu_Folefoc_Bilanda_Egbe_Werner_et al._2024, title={Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors}, volume={62}, DOI={<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>}, journal={Phytochemistry Letters}, publisher={Elsevier BV}, author={Nyemeck, Suzanne L. and Eyong, Kenneth O. and Bidingha, Ronald and Kamdem, Michael HK. and Ndinteh, Derek T. and Odumosu, Patricia O. and Folefoc, Gabriel N. and Bilanda, Danielle C. and Egbe, Andrew E. and Werner, Thomas and et al.}, year={2024}, pages={59–67} }","ama":"Nyemeck SL, Eyong KO, Bidingha R, et al. Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors. <i>Phytochemistry Letters</i>. 2024;62:59-67. doi:<a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>","ieee":"S. L. Nyemeck <i>et al.</i>, “Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors,” <i>Phytochemistry Letters</i>, vol. 62, pp. 59–67, 2024, doi: <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">10.1016/j.phytol.2024.06.004</a>.","apa":"Nyemeck, S. L., Eyong, K. O., Bidingha, R., Kamdem, M. HK., Ndinteh, D. T., Odumosu, P. O., Folefoc, G. N., Bilanda, D. C., Egbe, A. E., Werner, T., Bekono, B. D., &#38; Ntie-Kang, F. (2024). Design, isolation, synthesis, and mechanistic insight of flavonoids isolated from Beilschmiedia obscura, as potential α-glucosidase inhibitors. <i>Phytochemistry Letters</i>, <i>62</i>, 59–67. <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">https://doi.org/10.1016/j.phytol.2024.06.004</a>","short":"S.L. Nyemeck, K.O. Eyong, R. Bidingha, M.HK. Kamdem, D.T. Ndinteh, P.O. Odumosu, G.N. Folefoc, D.C. Bilanda, A.E. Egbe, T. Werner, B.D. Bekono, F. Ntie-Kang, Phytochemistry Letters 62 (2024) 59–67.","chicago":"Nyemeck, Suzanne L., Kenneth O. Eyong, Ronald Bidingha, Michael HK. Kamdem, Derek T. Ndinteh, Patricia O. Odumosu, Gabriel N. Folefoc, et al. “Design, Isolation, Synthesis, and Mechanistic Insight of Flavonoids Isolated from Beilschmiedia Obscura, as Potential α-Glucosidase Inhibitors.” <i>Phytochemistry Letters</i> 62 (2024): 59–67. <a href=\"https://doi.org/10.1016/j.phytol.2024.06.004\">https://doi.org/10.1016/j.phytol.2024.06.004</a>."}},{"status":"public","_id":"62094","publisher":"Elsevier BV","page":"26-35","volume":57,"user_id":"89271","citation":{"mla":"Yemback, Pierre, et al. “Lupane Derivatives: Design, Isolation, Synthesis and Evaluation of Antiplasmodial Activity against Plasmodium Falciparum 3D7 Strain.” <i>Phytochemistry Letters</i>, vol. 57, Elsevier BV, 2023, pp. 26–35, doi:<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>.","ama":"Yemback P, Eyong KO, Efange NM, et al. Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain. <i>Phytochemistry Letters</i>. 2023;57:26-35. doi:<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>","bibtex":"@article{Yemback_Eyong_Efange_Kamdem_Ndinteh_Odumosu_Folefoc_Ayong_Werner_2023, title={Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain}, volume={57}, DOI={<a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>}, journal={Phytochemistry Letters}, publisher={Elsevier BV}, author={Yemback, Pierre and Eyong, Kenneth O. and Efange, Noella M. and Kamdem, Michael HK. and Ndinteh, Derek T. and Odumosu, Patricia O. and Folefoc, Gabriel N. and Ayong, Lawrence and Werner, Thomas}, year={2023}, pages={26–35} }","apa":"Yemback, P., Eyong, K. O., Efange, N. M., Kamdem, M. HK., Ndinteh, D. T., Odumosu, P. O., Folefoc, G. N., Ayong, L., &#38; Werner, T. (2023). Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain. <i>Phytochemistry Letters</i>, <i>57</i>, 26–35. <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">https://doi.org/10.1016/j.phytol.2023.06.009</a>","ieee":"P. Yemback <i>et al.</i>, “Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain,” <i>Phytochemistry Letters</i>, vol. 57, pp. 26–35, 2023, doi: <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">10.1016/j.phytol.2023.06.009</a>.","chicago":"Yemback, Pierre, Kenneth O. Eyong, Noella M. Efange, Michael HK. Kamdem, Derek T. Ndinteh, Patricia O. Odumosu, Gabriel N. Folefoc, Lawrence Ayong, and Thomas Werner. “Lupane Derivatives: Design, Isolation, Synthesis and Evaluation of Antiplasmodial Activity against Plasmodium Falciparum 3D7 Strain.” <i>Phytochemistry Letters</i> 57 (2023): 26–35. <a href=\"https://doi.org/10.1016/j.phytol.2023.06.009\">https://doi.org/10.1016/j.phytol.2023.06.009</a>.","short":"P. Yemback, K.O. Eyong, N.M. Efange, M.HK. Kamdem, D.T. Ndinteh, P.O. Odumosu, G.N. Folefoc, L. Ayong, T. Werner, Phytochemistry Letters 57 (2023) 26–35."},"publication_identifier":{"issn":["1874-3900"]},"author":[{"full_name":"Yemback, Pierre","first_name":"Pierre","last_name":"Yemback"},{"last_name":"Eyong","first_name":"Kenneth O.","full_name":"Eyong, Kenneth O."},{"last_name":"Efange","first_name":"Noella M.","full_name":"Efange, Noella M."},{"full_name":"Kamdem, Michael HK.","last_name":"Kamdem","first_name":"Michael HK."},{"first_name":"Derek T.","last_name":"Ndinteh","full_name":"Ndinteh, Derek T."},{"first_name":"Patricia O.","last_name":"Odumosu","full_name":"Odumosu, Patricia O."},{"full_name":"Folefoc, Gabriel N.","first_name":"Gabriel N.","last_name":"Folefoc"},{"first_name":"Lawrence","last_name":"Ayong","full_name":"Ayong, Lawrence"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"year":"2023","title":"Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial activity against Plasmodium falciparum 3D7 strain","intvolume":"        57","date_updated":"2025-11-10T07:47:25Z","publication_status":"published","language":[{"iso":"eng"}],"doi":"10.1016/j.phytol.2023.06.009","publication":"Phytochemistry Letters","date_created":"2025-11-05T15:21:35Z","department":[{"_id":"35"},{"_id":"2"}],"type":"journal_article","keyword":["T4"]},{"abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>The biocatalytic kinetic resolution of cyclic carbonates derived from glycerol is reported. A selection of 26 esterases and lipases was tested for the asymmetric hydrolysis of the model substrate (epichlorohydrin carbonate) in aqueous medium. Among them, Pig Liver Esterase and Novozym® 435 showed the best selectivity with <jats:italic>E</jats:italic>=38 and 49, respectively. Both enzymes were employed for the conversion of 12 glycerol derivatives under optimized conditions. The resolution of halogenated carbonates afforded the unconverted enantiomer in up to &gt;99 : 1 <jats:italic>er</jats:italic>. Furthermore, Novozym® 435 was successfully recycled 10 times without significant loss of activity. Upscaling and isolation of the chiral carbonate was also demonstrated. Subsequent conversion of this chiral building block allowed the direct one‐pot synthesis of (<jats:italic>S</jats:italic>)‐Guaifenesin, (<jats:italic>S</jats:italic>)‐Mephenesin and (<jats:italic>S</jats:italic>)‐Chlorphenesin in up to 89 % yield and 94 : 6 <jats:italic>er</jats:italic>.</jats:p>"}],"issue":"19","publication":"ChemCatChem","department":[{"_id":"35"},{"_id":"2"}],"type":"journal_article","keyword":["T1","T4","CSSD"],"date_created":"2025-11-05T15:23:21Z","intvolume":"        15","date_updated":"2025-11-10T08:46:22Z","publication_status":"published","publication_identifier":{"issn":["1867-3880","1867-3899"]},"author":[{"first_name":"Constanza","last_name":"Terazzi","full_name":"Terazzi, Constanza"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"full_name":"von Langermann, Jan","last_name":"von Langermann","first_name":"Jan"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","id":"89271"}],"year":"2023","title":"Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates","doi":"10.1002/cctc.202300917","language":[{"iso":"eng"}],"article_number":"e202300917","citation":{"bibtex":"@article{Terazzi_Spannenberg_von Langermann_Werner_2023, title={Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates}, volume={15}, DOI={<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>}, number={19e202300917}, journal={ChemCatChem}, publisher={Wiley}, author={Terazzi, Constanza and Spannenberg, Anke and von Langermann, Jan and Werner, Thomas}, year={2023} }","ama":"Terazzi C, Spannenberg A, von Langermann J, Werner T. Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates. <i>ChemCatChem</i>. 2023;15(19). doi:<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>","mla":"Terazzi, Constanza, et al. “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates.” <i>ChemCatChem</i>, vol. 15, no. 19, e202300917, Wiley, 2023, doi:<a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>.","short":"C. Terazzi, A. Spannenberg, J. von Langermann, T. Werner, ChemCatChem 15 (2023).","chicago":"Terazzi, Constanza, Anke Spannenberg, Jan von Langermann, and Thomas Werner. “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates.” <i>ChemCatChem</i> 15, no. 19 (2023). <a href=\"https://doi.org/10.1002/cctc.202300917\">https://doi.org/10.1002/cctc.202300917</a>.","ieee":"C. Terazzi, A. Spannenberg, J. von Langermann, and T. Werner, “Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates,” <i>ChemCatChem</i>, vol. 15, no. 19, Art. no. e202300917, 2023, doi: <a href=\"https://doi.org/10.1002/cctc.202300917\">10.1002/cctc.202300917</a>.","apa":"Terazzi, C., Spannenberg, A., von Langermann, J., &#38; Werner, T. (2023). Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates. <i>ChemCatChem</i>, <i>15</i>(19), Article e202300917. <a href=\"https://doi.org/10.1002/cctc.202300917\">https://doi.org/10.1002/cctc.202300917</a>"},"status":"public","volume":15,"user_id":"89271","_id":"62096","publisher":"Wiley"},{"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>"}],"publication":"Synthesis","issue":"19","type":"journal_article","keyword":["T2","T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:27:34Z","publication_status":"published","date_updated":"2025-11-10T08:47:47Z","intvolume":"        53","year":"2021","title":"Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones","author":[{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"full_name":"Grandane, Aiga","first_name":"Aiga","last_name":"Grandane"},{"full_name":"Pudnika, Linda","last_name":"Pudnika","first_name":"Linda"},{"first_name":"Ilona","last_name":"Domraceva","full_name":"Domraceva, Ilona"},{"full_name":"Zalubovskis, Raivis","last_name":"Zalubovskis","first_name":"Raivis"}],"publication_identifier":{"issn":["0039-7881","1437-210X"]},"doi":"10.1055/a-1509-6078","language":[{"iso":"eng"}],"citation":{"apa":"Werner, T., Grandane, A., Pudnika, L., Domraceva, I., &#38; Zalubovskis, R. (2021). Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>, <i>53</i>(19), 3545–3554. <a href=\"https://doi.org/10.1055/a-1509-6078\">https://doi.org/10.1055/a-1509-6078</a>","ieee":"T. Werner, A. Grandane, L. Pudnika, I. Domraceva, and R. Zalubovskis, “Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones,” <i>Synthesis</i>, vol. 53, no. 19, pp. 3545–3554, 2021, doi: <a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>.","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>.","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>.","ama":"Werner T, Grandane A, Pudnika L, Domraceva I, Zalubovskis R. Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones. <i>Synthesis</i>. 2021;53(19):3545-3554. doi:<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>","bibtex":"@article{Werner_Grandane_Pudnika_Domraceva_Zalubovskis_2021, title={Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones}, volume={53}, DOI={<a href=\"https://doi.org/10.1055/a-1509-6078\">10.1055/a-1509-6078</a>}, number={19}, journal={Synthesis}, publisher={Georg Thieme Verlag KG}, author={Werner, Thomas and Grandane, Aiga and Pudnika, Linda and Domraceva, Ilona and Zalubovskis, Raivis}, year={2021}, pages={3545–3554} }"},"status":"public","user_id":"89271","volume":53,"page":"3545-3554","_id":"37946","publisher":"Georg Thieme Verlag KG"},{"publication":"Organic Process Research &amp; Development","issue":"1","type":"journal_article","keyword":["T4","CSSD"],"department":[{"_id":"35"},{"_id":"2"}],"date_created":"2025-11-05T15:26:05Z","publication_status":"published","date_updated":"2025-11-10T08:48:33Z","intvolume":"        25","title":"Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant","year":"2021","author":[{"last_name":"Stefanow","first_name":"Vivian","full_name":"Stefanow, Vivian"},{"full_name":"Grandane, Aiga","first_name":"Aiga","last_name":"Grandane"},{"first_name":"Marcus","last_name":"Eh","full_name":"Eh, Marcus"},{"last_name":"Panten","first_name":"Johannes","full_name":"Panten, Johannes"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1083-6160","1520-586X"]},"doi":"10.1021/acs.oprd.0c00423","language":[{"iso":"eng"}],"citation":{"ama":"Stefanow V, Grandane A, Eh M, Panten J, Spannenberg A, Werner T. 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Kanwischer, P. Gros, P. Leinweber, T. Werner, Ecotoxicology and Environmental Safety 225 (2021).","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). 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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>","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>.","short":"L. Longwitz, T. Werner, Angewandte Chemie 132 (2020) 2782–2785.","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>.","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>","ieee":"L. Longwitz and T. 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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"}],"publication":"Angewandte Chemie","issue":"7","keyword":["T2","T4"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"}],"date_created":"2025-11-05T15:39:06Z"},{"user_id":"89271","publication_date":"2022-01-06","_id":"62147","ipn":"WO2022/002380 A1","date_updated":"2025-11-10T08:10:00Z","author":[{"full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271"},{"full_name":"Stefanow, V.","first_name":"V.","last_name":"Stefanow"},{"full_name":"Grandane, A.","last_name":"Grandane","first_name":"A."},{"last_name":"Panten","first_name":"J.","full_name":"Panten, J."},{"last_name":"Eh","first_name":"M.","full_name":"Eh, M."}],"year":"2020","status":"public","title":"Novel processes for preparing cis-cedrandiol","department":[{"_id":"35"},{"_id":"2"}],"type":"patent","keyword":["T4"],"date_created":"2025-11-10T08:09:42Z","ipc":"-","citation":{"chicago":"Werner, Thomas, V. 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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"}],"issue":"7","publication":"Angewandte Chemie International Edition","volume":59,"user_id":"89271","publisher":"Wiley","_id":"62102","page":"2760-2763","status":"public","citation":{"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>.","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} }","ama":"Longwitz L, Werner T. 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