[{"doi":"10.1039/d0ob01492c","user_id":"53339","page":"7321-7325","language":[{"iso":"eng"}],"_id":"22234","date_updated":"2023-01-23T12:58:16Z","publication_status":"published","status":"public","year":"2020","title":"FLP-catalysis meets hydrogen-bond activation","publication_identifier":{"issn":["1477-0520","1477-0539"]},"author":[{"last_name":"Sitte","first_name":"Nikolai A.","full_name":"Sitte, Nikolai A."},{"last_name":"Köring","first_name":"Laura","full_name":"Köring, Laura"},{"full_name":"Roesky, Peter W.","last_name":"Roesky","first_name":"Peter W."},{"id":"53339","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan","full_name":"Paradies, Jan"}],"type":"journal_article","date_created":"2021-05-26T10:27:23Z","abstract":[{"lang":"eng","text":"<p>The potential of two chiral amidines and three non-chiral boranes in the metal-free hydrogen activation was explored.</p>"}],"publication":"Organic & Biomolecular Chemistry","citation":{"mla":"Sitte, Nikolai A., et al. “FLP-Catalysis Meets Hydrogen-Bond Activation.” <i>Organic &#38; Biomolecular Chemistry</i>, 2020, pp. 7321–25, doi:<a href=\"https://doi.org/10.1039/d0ob01492c\">10.1039/d0ob01492c</a>.","ama":"Sitte NA, Köring L, Roesky PW, Paradies J. FLP-catalysis meets hydrogen-bond activation. <i>Organic &#38; Biomolecular Chemistry</i>. Published online 2020:7321-7325. doi:<a href=\"https://doi.org/10.1039/d0ob01492c\">10.1039/d0ob01492c</a>","bibtex":"@article{Sitte_Köring_Roesky_Paradies_2020, title={FLP-catalysis meets hydrogen-bond activation}, DOI={<a href=\"https://doi.org/10.1039/d0ob01492c\">10.1039/d0ob01492c</a>}, journal={Organic &#38; Biomolecular Chemistry}, author={Sitte, Nikolai A. and Köring, Laura and Roesky, Peter W. and Paradies, Jan}, year={2020}, pages={7321–7325} }","apa":"Sitte, N. A., Köring, L., Roesky, P. W., &#38; Paradies, J. (2020). FLP-catalysis meets hydrogen-bond activation. <i>Organic &#38; Biomolecular Chemistry</i>, 7321–7325. <a href=\"https://doi.org/10.1039/d0ob01492c\">https://doi.org/10.1039/d0ob01492c</a>","ieee":"N. A. Sitte, L. Köring, P. W. Roesky, and J. Paradies, “FLP-catalysis meets hydrogen-bond activation,” <i>Organic &#38; Biomolecular Chemistry</i>, pp. 7321–7325, 2020, doi: <a href=\"https://doi.org/10.1039/d0ob01492c\">10.1039/d0ob01492c</a>.","chicago":"Sitte, Nikolai A., Laura Köring, Peter W. Roesky, and Jan Paradies. “FLP-Catalysis Meets Hydrogen-Bond Activation.” <i>Organic &#38; Biomolecular Chemistry</i>, 2020, 7321–25. <a href=\"https://doi.org/10.1039/d0ob01492c\">https://doi.org/10.1039/d0ob01492c</a>.","short":"N.A. Sitte, L. Köring, P.W. Roesky, J. Paradies, Organic &#38; Biomolecular Chemistry (2020) 7321–7325."}},{"type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:01:59Z","abstract":[{"text":"<p>The lithium <italic>tert</italic>-butoxide catalyzed addition of CS<sub>2</sub> to epoxides and thiiranes under mild conditions is reported. A mechanism has been proposed taking into account the regio- and stereochemical outcome of the reaction.</p>","lang":"eng"}],"extern":"1","publication":"Organic and Biomolecular Chemistry","issue":"31","doi":"10.1039/c6ob01081d","language":[{"iso":"eng"}],"date_updated":"2025-11-10T09:24:16Z","publication_status":"published","intvolume":"        14","year":"2016","title":"Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes","author":[{"first_name":"J.","last_name":"Diebler","full_name":"Diebler, J."},{"full_name":"Spannenberg, A.","last_name":"Spannenberg","first_name":"A."},{"id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"publication_identifier":{"issn":["1477-0520","1477-0539"]},"citation":{"mla":"Diebler, J., et al. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, Royal Society of Chemistry (RSC), 2016, pp. 7480–89, doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>.","bibtex":"@article{Diebler_Spannenberg_Werner_2016, title={Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes}, volume={14}, DOI={<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>}, number={31}, journal={Organic and Biomolecular Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Diebler, J. and Spannenberg, A. and Werner, Thomas}, year={2016}, pages={7480–7489} }","ama":"Diebler J, Spannenberg A, Werner T. Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>. 2016;14(31):7480-7489. doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>","ieee":"J. Diebler, A. Spannenberg, and T. Werner, “Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes,” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, pp. 7480–7489, 2016, doi: <a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>.","apa":"Diebler, J., Spannenberg, A., &#38; Werner, T. (2016). Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>, <i>14</i>(31), 7480–7489. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>","short":"J. Diebler, A. Spannenberg, T. Werner, Organic and Biomolecular Chemistry 14 (2016) 7480–7489.","chicago":"Diebler, J., A. Spannenberg, and Thomas Werner. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i> 14, no. 31 (2016): 7480–89. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>."},"user_id":"89271","volume":14,"page":"7480-7489","publisher":"Royal Society of Chemistry (RSC)","_id":"37981","status":"public"}]