@article{37945,
  abstract     = {{<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>}},
  author       = {{Tönjes, Jan and Longwitz, Lars and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T2, CSSD}},
  number       = {{13}},
  pages        = {{4852--4857}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction}}},
  doi          = {{10.1039/d1gc00953b}},
  volume       = {{23}},
  year         = {{2021}},
}

@article{62098,
  author       = {{Stefanow, Vivian and Grandane, Aiga and Eh, Marcus and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{1083-6160}},
  journal      = {{Organic Process Research &amp; Development}},
  keywords     = {{T4, CSSD}},
  number       = {{1}},
  pages        = {{89--97}},
  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}}},
  doi          = {{10.1021/acs.oprd.0c00423}},
  volume       = {{25}},
  year         = {{2021}},
}

@article{62099,
  author       = {{Stefanow, Vivian and Grandane, Aiga and Eh, Marcus and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{1083-6160}},
  journal      = {{Organic Process Research &amp; Development}},
  keywords     = {{T4, CSSD}},
  number       = {{1}},
  pages        = {{89--97}},
  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}}},
  doi          = {{10.1021/acs.oprd.0c00423}},
  volume       = {{25}},
  year         = {{2021}},
}

@article{37943,
  author       = {{Wirth, Marisa A. and Longwitz, Lars and Kanwischer, Marion and Gros, Peter and Leinweber, Peter and Werner, Thomas}},
  issn         = {{0147-6513}},
  journal      = {{Ecotoxicology and Environmental Safety}},
  keywords     = {{T4, CSSD}},
  publisher    = {{Elsevier BV}},
  title        = {{{AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate}}},
  doi          = {{10.1016/j.ecoenv.2021.112768}},
  volume       = {{225}},
  year         = {{2021}},
}

@article{37948,
  author       = {{Liu, Xin and Werner, Thomas}},
  issn         = {{1615-4150}},
  journal      = {{Advanced Synthesis and Catalysis}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{4}},
  pages        = {{1096--1104}},
  publisher    = {{Wiley}},
  title        = {{{Selective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides}}},
  doi          = {{10.1002/adsc.202001209}},
  volume       = {{363}},
  year         = {{2021}},
}

@article{62101,
  abstract     = {{<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>}},
  author       = {{Longwitz, Lars and Werner, Thomas}},
  issn         = {{0044-8249}},
  journal      = {{Angewandte Chemie}},
  keywords     = {{T2, T4}},
  number       = {{7}},
  pages        = {{2782--2785}},
  publisher    = {{Wiley}},
  title        = {{{Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis}}},
  doi          = {{10.1002/ange.201912991}},
  volume       = {{132}},
  year         = {{2020}},
}

@misc{62147,
  author       = {{Werner, Thomas and Stefanow, V. and Grandane, A. and Panten, J. and Eh, M.}},
  keywords     = {{T4}},
  title        = {{{Novel processes for preparing cis-cedrandiol}}},
  year         = {{2020}},
}

@article{37956,
  author       = {{Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Greb, Julian and Gulder, Tobias and Hüttel, Wolfgang and Kath‐Schorr, Stephanie and Kordes, Markus and Lehmann, Matthias and Lindel, Thomas and Luy, Burkhard and Mück‐Lichtenfeld, Christian and Muhle, Claudia and Narine, Arun and Niemeyer, Jörg and Paradies, Jan and Pfau, Roland and Pietruszka, Jörg and Schaschke, Norbert and Senge, Mathias and Straub, Bernd F. and Werner, Thomas and Werz, Daniel B. and Winter, Christian}},
  issn         = {{1439-9598}},
  journal      = {{Nachrichten aus der Chemie}},
  keywords     = {{General Chemical Engineering, General Chemistry}},
  number       = {{3}},
  pages        = {{42--72}},
  publisher    = {{Wiley}},
  title        = {{{Organische Chemie}}},
  doi          = {{10.1002/nadc.20204095515}},
  volume       = {{68}},
  year         = {{2020}},
}

@article{62102,
  abstract     = {{<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>}},
  author       = {{Longwitz, Lars and Werner, Thomas}},
  issn         = {{1433-7851}},
  journal      = {{Angewandte Chemie International Edition}},
  keywords     = {{T2, T4, CSSD}},
  number       = {{7}},
  pages        = {{2760--2763}},
  publisher    = {{Wiley}},
  title        = {{{Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling Catalysis}}},
  doi          = {{10.1002/anie.201912991}},
  volume       = {{59}},
  year         = {{2020}},
}

@article{37951,
  author       = {{Liu, Xin and Longwitz, Lars and Spiegelberg, Brian and Tönjes, Jan and Beweries, Torsten and Werner, Thomas}},
  issn         = {{2155-5435}},
  journal      = {{ACS Catalysis}},
  keywords     = {{T3, CSSD}},
  number       = {{22}},
  pages        = {{13659--13667}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions}}},
  doi          = {{10.1021/acscatal.0c03294}},
  volume       = {{10}},
  year         = {{2020}},
}

@article{37955,
  author       = {{Wulf, Christoph and Reckers, Matthias and Perechodjuk, Anna and Werner, Thomas}},
  issn         = {{2168-0485}},
  journal      = {{ACS Sustainable Chemistry and Engineering}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{3}},
  pages        = {{1651--1658}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes}}},
  doi          = {{10.1021/acssuschemeng.9b06662}},
  volume       = {{8}},
  year         = {{2020}},
}

@article{37953,
  author       = {{Hu, Yuya and Peglow, Sandra and Longwitz, Lars and Frank, Marcus and Epping, Jan Dirk and Brüser, Volker and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T2, T1, CSSD}},
  number       = {{7}},
  pages        = {{1825--1833}},
  publisher    = {{Wiley}},
  title        = {{{Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>}}},
  doi          = {{10.1002/cssc.201903384}},
  volume       = {{13}},
  year         = {{2020}},
}

@article{37952,
  author       = {{Grandane, Aiga and Nocentini, Alessio and Werner, Thomas and Zalubovskis, Raivis and Supuran, Claudiu T.}},
  issn         = {{0968-0896}},
  journal      = {{Bioorganic and Medicinal Chemistry}},
  keywords     = {{T4, T2, CSSD}},
  number       = {{11}},
  publisher    = {{Elsevier BV}},
  title        = {{{Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase inhibitors}}},
  doi          = {{10.1016/j.bmc.2020.115496}},
  volume       = {{28}},
  year         = {{2020}},
}

@article{37958,
  author       = {{Longwitz, Lars and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{2155-5435}},
  journal      = {{ACS Catalysis}},
  keywords     = {{T2, CSSD}},
  number       = {{10}},
  pages        = {{9237--9244}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature}}},
  doi          = {{10.1021/acscatal.9b02456}},
  volume       = {{9}},
  year         = {{2019}},
}

@article{37964,
  author       = {{Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Gulder, Tobias A. M. and Kath‐Schorr, Stephanie and Kordes, Markus and Lehmann, Matthias and Lindel, Thomas and Lüdeke, Steffen and Luy, Burkhard and Mantel, Marvin and Mück‐Lichtenfeld, Christian and Muhle‐Goll, Claudia and Narine, Arun and Niemeyer, Jochen and Pfau, Roland and Pietruszka, Jörg and Schaschke, Norbert and Senge, Mathias O. and Straub, Bernd F. and Werner, Thomas and Werz, Daniel B. and Winter, Christian}},
  issn         = {{1439-9598}},
  journal      = {{Nachrichten aus der Chemie}},
  keywords     = {{General Chemical Engineering, General Chemistry}},
  number       = {{3}},
  pages        = {{46--78}},
  publisher    = {{Wiley}},
  title        = {{{Trendbericht Organische Chemie}}},
  doi          = {{10.1002/nadc.20194085243}},
  volume       = {{67}},
  year         = {{2019}},
}

@article{37961,
  abstract     = {{<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>}},
  author       = {{Liu, Xin and de Vries, Johannes G. and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T3, CSSD}},
  number       = {{19}},
  pages        = {{5248--5255}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts}}},
  doi          = {{10.1039/c9gc02052g}},
  volume       = {{21}},
  year         = {{2019}},
}

@article{37963,
  author       = {{Büttner, Hendrik and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke, Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T4, CSSD}},
  number       = {{12}},
  pages        = {{2701--2707}},
  publisher    = {{Wiley}},
  title        = {{{Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate}}},
  doi          = {{10.1002/cssc.201900678}},
  volume       = {{12}},
  year         = {{2019}},
}

@article{37957,
  author       = {{Hu, Yuya and Steinbauer, Johannes and Stefanow, Vivian and Spannenberg, Anke and Werner, Thomas}},
  issn         = {{2168-0485}},
  journal      = {{ACS Sustainable Chemistry and Engineering}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{15}},
  pages        = {{13257--13269}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Polyethers as Complexing Agents in Calcium-Catalyzed Cyclic Carbonate Synthesis}}},
  doi          = {{10.1021/acssuschemeng.9b02502}},
  volume       = {{7}},
  year         = {{2019}},
}

@article{37962,
  author       = {{Longwitz, Lars and Jopp, Stefan and Werner, Thomas}},
  issn         = {{0022-3263}},
  journal      = {{The Journal of Organic Chemistry}},
  keywords     = {{T2, CSSD}},
  number       = {{12}},
  pages        = {{7863--7870}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling}}},
  doi          = {{10.1021/acs.joc.9b00741}},
  volume       = {{84}},
  year         = {{2019}},
}

@article{37959,
  abstract     = {{<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>}},
  author       = {{Longwitz, Lars and Werner, Thomas}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  keywords     = {{T2, CSSD}},
  number       = {{6456}},
  pages        = {{866--867}},
  publisher    = {{American Association for the Advancement of Science (AAAS)}},
  title        = {{{The Mitsunobu reaction, reimagined}}},
  doi          = {{10.1126/science.aay6635}},
  volume       = {{365}},
  year         = {{2019}},
}