@article{62090,
  abstract     = {{<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>}},
  author       = {{Ren, Changyue and Terazzi, Constanza and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{1}},
  pages        = {{439--447}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Tuneable reduction of CO<sub>2</sub> – organocatalyzed selective formylation and methylation of amines}}},
  doi          = {{10.1039/d3gc03993e}},
  volume       = {{26}},
  year         = {{2024}},
}

@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{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{37973,
  abstract     = {{<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>}},
  author       = {{Steinbauer, J. and Longwitz, L. and Frank, M. and Epping, J. and Kragl, U. and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{18}},
  pages        = {{4435--4445}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides}}},
  doi          = {{10.1039/c7gc01782k}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37975,
  abstract     = {{<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>}},
  author       = {{Steinbauer, J. and Spannenberg, A. and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{16}},
  pages        = {{3769--3779}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  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}},
  volume       = {{19}},
  year         = {{2017}},
}

@article{37983,
  abstract     = {{<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>}},
  author       = {{Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}},
  issn         = {{1463-9262}},
  journal      = {{Green Chemistry}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{13}},
  pages        = {{3775--3788}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables}}},
  doi          = {{10.1039/c6gc00671j}},
  volume       = {{18}},
  year         = {{2016}},
}