---
_id: '62086'
author:
- first_name: Vivian
  full_name: Stefanow, Vivian
  last_name: Stefanow
- first_name: Lukas
  full_name: Kell, Lukas
  last_name: Kell
- first_name: Aiga
  full_name: Leduskrasta, Aiga
  last_name: Leduskrasta
- first_name: Marcus
  full_name: Eh, Marcus
  last_name: Eh
- first_name: Johannes
  full_name: Panten, Johannes
  last_name: Panten
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  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>
  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>
  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}
    }'
  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>.'
  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>.'
  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>.
  short: V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, T. Werner, The Journal
    of Organic Chemistry 90 (2025) 12877–12887.
date_created: 2025-11-05T15:10:13Z
date_updated: 2025-11-10T08:43:33Z
department:
- _id: '35'
- _id: '2'
doi: 10.1021/acs.joc.5c00889
intvolume: '        90'
issue: '37'
keyword:
- T4
- CSSD
language:
- iso: eng
page: 12877-12887
publication: The Journal of Organic Chemistry
publication_identifier:
  issn:
  - 0022-3263
  - 1520-6904
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance
  Ingredients
type: journal_article
user_id: '89271'
volume: 90
year: '2025'
...
---
_id: '62092'
author:
- first_name: Suzanne L.
  full_name: Nyemeck, Suzanne L.
  last_name: Nyemeck
- first_name: Kenneth O.
  full_name: Eyong, Kenneth O.
  last_name: Eyong
- first_name: Ronald
  full_name: Bidingha, Ronald
  last_name: Bidingha
- first_name: Michael HK.
  full_name: Kamdem, Michael HK.
  last_name: Kamdem
- first_name: Derek T.
  full_name: Ndinteh, Derek T.
  last_name: Ndinteh
- first_name: Patricia O.
  full_name: Odumosu, Patricia O.
  last_name: Odumosu
- first_name: Gabriel N.
  full_name: Folefoc, Gabriel N.
  last_name: Folefoc
- first_name: Danielle C.
  full_name: Bilanda, Danielle C.
  last_name: Bilanda
- first_name: Andrew E.
  full_name: Egbe, Andrew E.
  last_name: Egbe
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
- first_name: Boris D.
  full_name: Bekono, Boris D.
  last_name: Bekono
- first_name: Fidele
  full_name: Ntie-Kang, Fidele
  last_name: Ntie-Kang
citation:
  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>
  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>
  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}
    }'
  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>.'
  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>.'
  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>.
  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.
date_created: 2025-11-05T15:18:32Z
date_updated: 2025-11-10T07:45:58Z
department:
- _id: '35'
- _id: '2'
doi: 10.1016/j.phytol.2024.06.004
intvolume: '        62'
keyword:
- T4
language:
- iso: eng
page: 59-67
publication: Phytochemistry Letters
publication_identifier:
  issn:
  - 1874-3900
publication_status: published
publisher: Elsevier BV
status: public
title: Design, isolation, synthesis, and mechanistic insight of flavonoids isolated
  from Beilschmiedia obscura, as potential α-glucosidase inhibitors
type: journal_article
user_id: '89271'
volume: 62
year: '2024'
...
---
_id: '62094'
author:
- first_name: Pierre
  full_name: Yemback, Pierre
  last_name: Yemback
- first_name: Kenneth O.
  full_name: Eyong, Kenneth O.
  last_name: Eyong
- first_name: Noella M.
  full_name: Efange, Noella M.
  last_name: Efange
- first_name: Michael HK.
  full_name: Kamdem, Michael HK.
  last_name: Kamdem
- first_name: Derek T.
  full_name: Ndinteh, Derek T.
  last_name: Ndinteh
- first_name: Patricia O.
  full_name: Odumosu, Patricia O.
  last_name: Odumosu
- first_name: Gabriel N.
  full_name: Folefoc, Gabriel N.
  last_name: Folefoc
- first_name: Lawrence
  full_name: Ayong, Lawrence
  last_name: Ayong
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  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>'
  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>'
  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} }'
  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>.'
  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>.'
  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>.'
  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.
date_created: 2025-11-05T15:21:35Z
date_updated: 2025-11-10T07:47:25Z
department:
- _id: '35'
- _id: '2'
doi: 10.1016/j.phytol.2023.06.009
intvolume: '        57'
keyword:
- T4
language:
- iso: eng
page: 26-35
publication: Phytochemistry Letters
publication_identifier:
  issn:
  - 1874-3900
publication_status: published
publisher: Elsevier BV
status: public
title: 'Lupane derivatives: Design, isolation, synthesis and evaluation of antiplasmodial
  activity against Plasmodium falciparum 3D7 strain'
type: journal_article
user_id: '89271'
volume: 57
year: '2023'
...
---
_id: '62096'
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>
article_number: e202300917
author:
- first_name: Constanza
  full_name: Terazzi, Constanza
  last_name: Terazzi
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Jan
  full_name: von Langermann, Jan
  last_name: von Langermann
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  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>
  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>
  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}
    }'
  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>.'
  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).
date_created: 2025-11-05T15:23:21Z
date_updated: 2025-11-10T08:46:22Z
department:
- _id: '35'
- _id: '2'
doi: 10.1002/cctc.202300917
intvolume: '        15'
issue: '19'
keyword:
- T1
- T4
- CSSD
language:
- iso: eng
publication: ChemCatChem
publication_identifier:
  issn:
  - 1867-3880
  - 1867-3899
publication_status: published
publisher: Wiley
status: public
title: Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution
  of Glycerol‐Derived Cyclic Carbonates
type: journal_article
user_id: '89271'
volume: 15
year: '2023'
...
---
_id: '37946'
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>
author:
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
- first_name: Aiga
  full_name: Grandane, Aiga
  last_name: Grandane
- first_name: Linda
  full_name: Pudnika, Linda
  last_name: Pudnika
- first_name: Ilona
  full_name: Domraceva, Ilona
  last_name: Domraceva
- first_name: Raivis
  full_name: Zalubovskis, Raivis
  last_name: Zalubovskis
citation:
  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>
  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>
  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} }'
  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>.'
  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>.'
  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>.
  short: T. Werner, A. Grandane, L. Pudnika, I. Domraceva, R. Zalubovskis, Synthesis
    53 (2021) 3545–3554.
date_created: 2023-01-22T20:27:34Z
date_updated: 2025-11-10T08:47:47Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1055/a-1509-6078
intvolume: '        53'
issue: '19'
keyword:
- T2
- T4
- CSSD
language:
- iso: eng
page: 3545-3554
publication: Synthesis
publication_identifier:
  issn:
  - 0039-7881
  - 1437-210X
publication_status: published
publisher: Georg Thieme Verlag KG
status: public
title: Base-Free Catalytic Wittig-/Cross-Coupling Reaction Sequence as Short Synthetic
  Strategy for the Preparation of Highly Functionalized Arylbenzoxepinones
type: journal_article
user_id: '89271'
volume: 53
year: '2021'
...
---
_id: '62098'
author:
- first_name: Vivian
  full_name: Stefanow, Vivian
  last_name: Stefanow
- first_name: Aiga
  full_name: Grandane, Aiga
  last_name: Grandane
- first_name: Marcus
  full_name: Eh, Marcus
  last_name: Eh
- first_name: Johannes
  full_name: Panten, Johannes
  last_name: Panten
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Stefanow V, Grandane A, Eh M, Panten J, Spannenberg A, Werner T. Stereoselective
    Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant.
    <i>Organic Process Research &#38;amp; Development</i>. 2021;25(1):89-97. doi:<a
    href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>
  apa: Stefanow, V., Grandane, A., Eh, M., Panten, J., Spannenberg, A., &#38; Werner,
    T. (2021). Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key
    Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>,
    <i>25</i>(1), 89–97. <a href="https://doi.org/10.1021/acs.oprd.0c00423">https://doi.org/10.1021/acs.oprd.0c00423</a>
  bibtex: '@article{Stefanow_Grandane_Eh_Panten_Spannenberg_Werner_2021, title={Stereoselective
    Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant},
    volume={25}, DOI={<a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>},
    number={1}, journal={Organic Process Research &#38;amp; Development}, publisher={American
    Chemical Society (ACS)}, author={Stefanow, Vivian and Grandane, Aiga and Eh, Marcus
    and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2021}, pages={89–97}
    }'
  chicago: 'Stefanow, Vivian, Aiga Grandane, Marcus Eh, Johannes Panten, Anke Spannenberg,
    and Thomas Werner. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol
    as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp;
    Development</i> 25, no. 1 (2021): 89–97. <a href="https://doi.org/10.1021/acs.oprd.0c00423">https://doi.org/10.1021/acs.oprd.0c00423</a>.'
  ieee: 'V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, and T. Werner,
    “Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate
    for an Amber Odorant,” <i>Organic Process Research &#38;amp; Development</i>,
    vol. 25, no. 1, pp. 89–97, 2021, doi: <a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>.'
  mla: Stefanow, Vivian, et al. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol
    as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp;
    Development</i>, vol. 25, no. 1, American Chemical Society (ACS), 2021, pp. 89–97,
    doi:<a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>.
  short: V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, T. Werner, Organic
    Process Research &#38;amp; Development 25 (2021) 89–97.
date_created: 2025-11-05T15:26:05Z
date_updated: 2025-11-10T08:48:33Z
department:
- _id: '35'
- _id: '2'
doi: 10.1021/acs.oprd.0c00423
intvolume: '        25'
issue: '1'
keyword:
- T4
- CSSD
language:
- iso: eng
page: 89-97
publication: Organic Process Research &amp; Development
publication_identifier:
  issn:
  - 1083-6160
  - 1520-586X
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate
  for an Amber Odorant
type: journal_article
user_id: '89271'
volume: 25
year: '2021'
...
---
_id: '62099'
author:
- first_name: Vivian
  full_name: Stefanow, Vivian
  last_name: Stefanow
- first_name: Aiga
  full_name: Grandane, Aiga
  last_name: Grandane
- first_name: Marcus
  full_name: Eh, Marcus
  last_name: Eh
- first_name: Johannes
  full_name: Panten, Johannes
  last_name: Panten
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Stefanow V, Grandane A, Eh M, Panten J, Spannenberg A, Werner T. Stereoselective
    Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant.
    <i>Organic Process Research &#38;amp; Development</i>. 2021;25(1):89-97. doi:<a
    href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>
  apa: Stefanow, V., Grandane, A., Eh, M., Panten, J., Spannenberg, A., &#38; Werner,
    T. (2021). Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key
    Intermediate for an Amber Odorant. <i>Organic Process Research &#38;amp; Development</i>,
    <i>25</i>(1), 89–97. <a href="https://doi.org/10.1021/acs.oprd.0c00423">https://doi.org/10.1021/acs.oprd.0c00423</a>
  bibtex: '@article{Stefanow_Grandane_Eh_Panten_Spannenberg_Werner_2021, title={Stereoselective
    Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate for an Amber Odorant},
    volume={25}, DOI={<a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>},
    number={1}, journal={Organic Process Research &#38;amp; Development}, publisher={American
    Chemical Society (ACS)}, author={Stefanow, Vivian and Grandane, Aiga and Eh, Marcus
    and Panten, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2021}, pages={89–97}
    }'
  chicago: 'Stefanow, Vivian, Aiga Grandane, Marcus Eh, Johannes Panten, Anke Spannenberg,
    and Thomas Werner. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol
    as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp;
    Development</i> 25, no. 1 (2021): 89–97. <a href="https://doi.org/10.1021/acs.oprd.0c00423">https://doi.org/10.1021/acs.oprd.0c00423</a>.'
  ieee: 'V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, and T. Werner,
    “Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate
    for an Amber Odorant,” <i>Organic Process Research &#38;amp; Development</i>,
    vol. 25, no. 1, pp. 89–97, 2021, doi: <a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>.'
  mla: Stefanow, Vivian, et al. “Stereoselective Synthesis of a<i>Cis</i>-Cedrane-8,9-Diol
    as a Key Intermediate for an Amber Odorant.” <i>Organic Process Research &#38;amp;
    Development</i>, vol. 25, no. 1, American Chemical Society (ACS), 2021, pp. 89–97,
    doi:<a href="https://doi.org/10.1021/acs.oprd.0c00423">10.1021/acs.oprd.0c00423</a>.
  short: V. Stefanow, A. Grandane, M. Eh, J. Panten, A. Spannenberg, T. Werner, Organic
    Process Research &#38;amp; Development 25 (2021) 89–97.
date_created: 2025-11-05T15:28:23Z
date_updated: 2025-11-10T08:49:27Z
department:
- _id: '35'
- _id: '2'
doi: 10.1021/acs.oprd.0c00423
intvolume: '        25'
issue: '1'
keyword:
- T4
- CSSD
language:
- iso: eng
page: 89-97
publication: Organic Process Research &amp; Development
publication_identifier:
  issn:
  - 1083-6160
  - 1520-586X
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Stereoselective Synthesis of a<i>cis</i>-Cedrane-8,9-diol as a Key Intermediate
  for an Amber Odorant
type: journal_article
user_id: '89271'
volume: 25
year: '2021'
...
---
_id: '37943'
article_number: '112768'
author:
- first_name: Marisa A.
  full_name: Wirth, Marisa A.
  last_name: Wirth
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Marion
  full_name: Kanwischer, Marion
  last_name: Kanwischer
- first_name: Peter
  full_name: Gros, Peter
  last_name: Gros
- first_name: Peter
  full_name: Leinweber, Peter
  last_name: Leinweber
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: https://orcid.org/0000-0001-9025-3244
citation:
  ama: Wirth MA, Longwitz L, Kanwischer M, Gros P, Leinweber P, Werner T. AMPA-15N
    – Synthesis and application as standard compound in traceable degradation studies
    of glyphosate. <i>Ecotoxicology and Environmental Safety</i>. 2021;225. 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). AMPA-15N – Synthesis and application as standard compound in
    traceable degradation studies of glyphosate. <i>Ecotoxicology and Environmental
    Safety</i>, <i>225</i>, Article 112768. <a href="https://doi.org/10.1016/j.ecoenv.2021.112768">https://doi.org/10.1016/j.ecoenv.2021.112768</a>
  bibtex: '@article{Wirth_Longwitz_Kanwischer_Gros_Leinweber_Werner_2021, title={AMPA-15N
    – Synthesis and application as standard compound in traceable degradation studies
    of glyphosate}, volume={225}, DOI={<a href="https://doi.org/10.1016/j.ecoenv.2021.112768">10.1016/j.ecoenv.2021.112768</a>},
    number={112768}, journal={Ecotoxicology and Environmental Safety}, publisher={Elsevier
    BV}, author={Wirth, Marisa A. and Longwitz, Lars and Kanwischer, Marion and Gros,
    Peter and Leinweber, Peter and Werner, Thomas}, year={2021} }'
  chicago: Wirth, Marisa A., Lars Longwitz, Marion Kanwischer, Peter Gros, Peter Leinweber,
    and Thomas Werner. “AMPA-15N – Synthesis and Application as Standard Compound
    in Traceable Degradation Studies of Glyphosate.” <i>Ecotoxicology and Environmental
    Safety</i> 225 (2021). <a href="https://doi.org/10.1016/j.ecoenv.2021.112768">https://doi.org/10.1016/j.ecoenv.2021.112768</a>.
  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>.'
  mla: Wirth, Marisa A., et al. “AMPA-15N – Synthesis and Application as Standard
    Compound in Traceable Degradation Studies of Glyphosate.” <i>Ecotoxicology and
    Environmental Safety</i>, vol. 225, 112768, Elsevier BV, 2021, doi:<a href="https://doi.org/10.1016/j.ecoenv.2021.112768">10.1016/j.ecoenv.2021.112768</a>.
  short: M.A. Wirth, L. Longwitz, M. Kanwischer, P. Gros, P. Leinweber, T. Werner,
    Ecotoxicology and Environmental Safety 225 (2021).
date_created: 2023-01-22T20:23:06Z
date_updated: 2025-11-10T08:48:20Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1016/j.ecoenv.2021.112768
intvolume: '       225'
keyword:
- T4
- CSSD
language:
- iso: eng
publication: Ecotoxicology and Environmental Safety
publication_identifier:
  issn:
  - 0147-6513
publication_status: published
publisher: Elsevier BV
status: public
title: AMPA-15N – Synthesis and application as standard compound in traceable degradation
  studies of glyphosate
type: journal_article
user_id: '89271'
volume: 225
year: '2021'
...
---
_id: '62101'
abstract:
- lang: eng
  text: <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:
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Longwitz L, Werner T. 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>
  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>
  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} }'
  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>.'
  ieee: 'L. Longwitz and T. 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, pp. 2782–2785,
    2020, doi: <a href="https://doi.org/10.1002/ange.201912991">10.1002/ange.201912991</a>.'
  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.
date_created: 2025-11-05T15:39:06Z
date_updated: 2025-11-10T08:11:23Z
department:
- _id: '35'
- _id: '2'
doi: 10.1002/ange.201912991
intvolume: '       132'
issue: '7'
keyword:
- T2
- T4
language:
- iso: eng
page: 2782-2785
publication: Angewandte Chemie
publication_identifier:
  issn:
  - 0044-8249
  - 1521-3757
publication_status: published
publisher: Wiley
status: public
title: Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling
  Catalysis
type: journal_article
user_id: '89271'
volume: 132
year: '2020'
...
---
_id: '62147'
author:
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
- first_name: V.
  full_name: Stefanow, V.
  last_name: Stefanow
- first_name: A.
  full_name: Grandane, A.
  last_name: Grandane
- first_name: J.
  full_name: Panten, J.
  last_name: Panten
- first_name: M.
  full_name: Eh, M.
  last_name: Eh
citation:
  ama: Werner T, Stefanow V, Grandane A, Panten J, Eh M. Novel processes for preparing
    cis-cedrandiol. Published online 2020.
  apa: Werner, T., Stefanow, V., Grandane, A., Panten, J., &#38; Eh, M. (2020). <i>Novel
    processes for preparing cis-cedrandiol</i>.
  bibtex: '@article{Werner_Stefanow_Grandane_Panten_Eh_2020, title={Novel processes
    for preparing cis-cedrandiol}, author={Werner, Thomas and Stefanow, V. and Grandane,
    A. and Panten, J. and Eh, M.}, year={2020} }'
  chicago: Werner, Thomas, V. Stefanow, A. Grandane, J. Panten, and M. Eh. “Novel
    Processes for Preparing Cis-Cedrandiol,” 2020.
  ieee: T. Werner, V. Stefanow, A. Grandane, J. Panten, and M. Eh, “Novel processes
    for preparing cis-cedrandiol.” 2020.
  mla: Werner, Thomas, et al. <i>Novel Processes for Preparing Cis-Cedrandiol</i>.
    2020.
  short: T. Werner, V. Stefanow, A. Grandane, J. Panten, M. Eh, (2020).
date_created: 2025-11-10T08:09:42Z
date_updated: 2025-11-10T08:10:00Z
department:
- _id: '35'
- _id: '2'
ipc: '-'
ipn: WO2022/002380 A1
keyword:
- T4
publication_date: 2022-01-06
status: public
title: Novel processes for preparing cis-cedrandiol
type: patent
user_id: '89271'
year: '2020'
...
---
_id: '62102'
abstract:
- lang: eng
  text: <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:
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Longwitz L, Werner T. Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup>
    Redox Cycling Catalysis. <i>Angewandte Chemie International Edition</i>. 2020;59(7):2760-2763.
    doi:<a href="https://doi.org/10.1002/anie.201912991">10.1002/anie.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 International Edition</i>, <i>59</i>(7),
    2760–2763. <a href="https://doi.org/10.1002/anie.201912991">https://doi.org/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} }'
  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 International
    Edition</i> 59, no. 7 (2020): 2760–63. <a href="https://doi.org/10.1002/anie.201912991">https://doi.org/10.1002/anie.201912991</a>.'
  ieee: 'L. Longwitz and T. 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, pp. 2760–2763, 2020, doi: <a href="https://doi.org/10.1002/anie.201912991">10.1002/anie.201912991</a>.'
  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>.
  short: L. Longwitz, T. Werner, Angewandte Chemie International Edition 59 (2020)
    2760–2763.
date_created: 2025-11-05T15:39:56Z
date_updated: 2025-11-10T08:49:52Z
department:
- _id: '35'
- _id: '2'
doi: 10.1002/anie.201912991
intvolume: '        59'
issue: '7'
keyword:
- T2
- T4
- CSSD
language:
- iso: eng
page: 2760-2763
publication: Angewandte Chemie International Edition
publication_identifier:
  issn:
  - 1433-7851
  - 1521-3773
publication_status: published
publisher: Wiley
status: public
title: Reduction of Activated Alkenes by P<sup>III</sup>/P<sup>V</sup> Redox Cycling
  Catalysis
type: journal_article
user_id: '89271'
volume: 59
year: '2020'
...
---
_id: '37952'
article_number: '115496'
author:
- first_name: Aiga
  full_name: Grandane, Aiga
  last_name: Grandane
- first_name: Alessio
  full_name: Nocentini, Alessio
  last_name: Nocentini
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
- first_name: Raivis
  full_name: Zalubovskis, Raivis
  last_name: Zalubovskis
- first_name: Claudiu T.
  full_name: Supuran, Claudiu T.
  last_name: Supuran
citation:
  ama: 'Grandane A, Nocentini A, Werner T, Zalubovskis R, Supuran CT. Benzoxepinones:
    A new isoform-selective class of tumor associated carbonic anhydrase inhibitors.
    <i>Bioorganic and Medicinal Chemistry</i>. 2020;28(11). doi:<a href="https://doi.org/10.1016/j.bmc.2020.115496">10.1016/j.bmc.2020.115496</a>'
  apa: 'Grandane, A., Nocentini, A., Werner, T., Zalubovskis, R., &#38; Supuran, C.
    T. (2020). Benzoxepinones: A new isoform-selective class of tumor associated carbonic
    anhydrase inhibitors. <i>Bioorganic and Medicinal Chemistry</i>, <i>28</i>(11),
    Article 115496. <a href="https://doi.org/10.1016/j.bmc.2020.115496">https://doi.org/10.1016/j.bmc.2020.115496</a>'
  bibtex: '@article{Grandane_Nocentini_Werner_Zalubovskis_Supuran_2020, title={Benzoxepinones:
    A new isoform-selective class of tumor associated carbonic anhydrase inhibitors},
    volume={28}, DOI={<a href="https://doi.org/10.1016/j.bmc.2020.115496">10.1016/j.bmc.2020.115496</a>},
    number={11115496}, journal={Bioorganic and Medicinal Chemistry}, publisher={Elsevier
    BV}, author={Grandane, Aiga and Nocentini, Alessio and Werner, Thomas and Zalubovskis,
    Raivis and Supuran, Claudiu T.}, year={2020} }'
  chicago: 'Grandane, Aiga, Alessio Nocentini, Thomas Werner, Raivis Zalubovskis,
    and Claudiu T. Supuran. “Benzoxepinones: A New Isoform-Selective Class of Tumor
    Associated Carbonic Anhydrase Inhibitors.” <i>Bioorganic and Medicinal Chemistry</i>
    28, no. 11 (2020). <a href="https://doi.org/10.1016/j.bmc.2020.115496">https://doi.org/10.1016/j.bmc.2020.115496</a>.'
  ieee: 'A. Grandane, A. Nocentini, T. Werner, R. Zalubovskis, and C. T. Supuran,
    “Benzoxepinones: A new isoform-selective class of tumor associated carbonic anhydrase
    inhibitors,” <i>Bioorganic and Medicinal Chemistry</i>, vol. 28, no. 11, Art.
    no. 115496, 2020, doi: <a href="https://doi.org/10.1016/j.bmc.2020.115496">10.1016/j.bmc.2020.115496</a>.'
  mla: 'Grandane, Aiga, et al. “Benzoxepinones: A New Isoform-Selective Class of Tumor
    Associated Carbonic Anhydrase Inhibitors.” <i>Bioorganic and Medicinal Chemistry</i>,
    vol. 28, no. 11, 115496, Elsevier BV, 2020, doi:<a href="https://doi.org/10.1016/j.bmc.2020.115496">10.1016/j.bmc.2020.115496</a>.'
  short: A. Grandane, A. Nocentini, T. Werner, R. Zalubovskis, C.T. Supuran, Bioorganic
    and Medicinal Chemistry 28 (2020).
date_created: 2023-01-22T20:36:02Z
date_updated: 2025-11-10T08:51:24Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1016/j.bmc.2020.115496
extern: '1'
intvolume: '        28'
issue: '11'
keyword:
- T4
- T2
- CSSD
language:
- iso: eng
publication: Bioorganic and Medicinal Chemistry
publication_identifier:
  issn:
  - 0968-0896
publication_status: published
publisher: Elsevier BV
status: public
title: 'Benzoxepinones: A new isoform-selective class of tumor associated carbonic
  anhydrase inhibitors'
type: journal_article
user_id: '89271'
volume: 28
year: '2020'
...
---
_id: '37963'
author:
- first_name: Hendrik
  full_name: Büttner, Hendrik
  last_name: Büttner
- first_name: Christina
  full_name: Kohrt, Christina
  last_name: Kohrt
- first_name: Christoph
  full_name: Wulf, Christoph
  last_name: Wulf
- first_name: Benjamin
  full_name: Schäffner, Benjamin
  last_name: Schäffner
- first_name: Karsten
  full_name: Groenke, Karsten
  last_name: Groenke
- first_name: Yuya
  full_name: Hu, Yuya
  last_name: Hu
- first_name: Daniela
  full_name: Kruse, Daniela
  last_name: Kruse
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Büttner H, Kohrt C, Wulf C, et al. Life Cycle Assessment for the Organocatalytic
    Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>. 2019;12(12):2701-2707.
    doi:<a href="https://doi.org/10.1002/cssc.201900678">10.1002/cssc.201900678</a>
  apa: Büttner, H., Kohrt, C., Wulf, C., Schäffner, B., Groenke, K., Hu, Y., Kruse,
    D., &#38; Werner, T. (2019). Life Cycle Assessment for the Organocatalytic Synthesis
    of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>, <i>12</i>(12), 2701–2707.
    <a href="https://doi.org/10.1002/cssc.201900678">https://doi.org/10.1002/cssc.201900678</a>
  bibtex: '@article{Büttner_Kohrt_Wulf_Schäffner_Groenke_Hu_Kruse_Werner_2019, title={Life
    Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate},
    volume={12}, DOI={<a href="https://doi.org/10.1002/cssc.201900678">10.1002/cssc.201900678</a>},
    number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik
    and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke,
    Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}, year={2019}, pages={2701–2707}
    }'
  chicago: 'Büttner, Hendrik, Christina Kohrt, Christoph Wulf, Benjamin Schäffner,
    Karsten Groenke, Yuya Hu, Daniela Kruse, and Thomas Werner. “Life Cycle Assessment
    for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i>
    12, no. 12 (2019): 2701–7. <a href="https://doi.org/10.1002/cssc.201900678">https://doi.org/10.1002/cssc.201900678</a>.'
  ieee: 'H. Büttner <i>et al.</i>, “Life Cycle Assessment for the Organocatalytic
    Synthesis of Glycerol Carbonate Methacrylate,” <i>ChemSusChem</i>, vol. 12, no.
    12, pp. 2701–2707, 2019, doi: <a href="https://doi.org/10.1002/cssc.201900678">10.1002/cssc.201900678</a>.'
  mla: Büttner, Hendrik, et al. “Life Cycle Assessment for the Organocatalytic Synthesis
    of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i>, vol. 12, no. 12, Wiley,
    2019, pp. 2701–07, doi:<a href="https://doi.org/10.1002/cssc.201900678">10.1002/cssc.201900678</a>.
  short: H. Büttner, C. Kohrt, C. Wulf, B. Schäffner, K. Groenke, Y. Hu, D. Kruse,
    T. Werner, ChemSusChem 12 (2019) 2701–2707.
date_created: 2023-01-22T20:44:24Z
date_updated: 2025-11-10T08:56:56Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1002/cssc.201900678
extern: '1'
intvolume: '        12'
issue: '12'
keyword:
- T1
- T4
- CSSD
language:
- iso: eng
page: 2701-2707
publication: ChemSusChem
publication_identifier:
  issn:
  - 1864-5631
  - 1864-564X
publication_status: published
publisher: Wiley
status: public
title: Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate
  Methacrylate
type: journal_article
user_id: '89271'
volume: 12
year: '2019'
...
---
_id: '37960'
author:
- first_name: Bernhard M.
  full_name: Stadler, Bernhard M.
  last_name: Stadler
- first_name: Christoph
  full_name: Wulf, Christoph
  last_name: Wulf
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
- first_name: Sergey
  full_name: Tin, Sergey
  last_name: Tin
- first_name: Johannes G.
  full_name: de Vries, Johannes G.
  last_name: de Vries
citation:
  ama: Stadler BM, Wulf C, Werner T, Tin S, de Vries JG. Catalytic Approaches to Monomers
    for Polymers Based on Renewables. <i>ACS Catalysis</i>. 2019;9(9):8012-8067. doi:<a
    href="https://doi.org/10.1021/acscatal.9b01665">10.1021/acscatal.9b01665</a>
  apa: Stadler, B. M., Wulf, C., Werner, T., Tin, S., &#38; de Vries, J. G. (2019).
    Catalytic Approaches to Monomers for Polymers Based on Renewables. <i>ACS Catalysis</i>,
    <i>9</i>(9), 8012–8067. <a href="https://doi.org/10.1021/acscatal.9b01665">https://doi.org/10.1021/acscatal.9b01665</a>
  bibtex: '@article{Stadler_Wulf_Werner_Tin_de Vries_2019, title={Catalytic Approaches
    to Monomers for Polymers Based on Renewables}, volume={9}, DOI={<a href="https://doi.org/10.1021/acscatal.9b01665">10.1021/acscatal.9b01665</a>},
    number={9}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)},
    author={Stadler, Bernhard M. and Wulf, Christoph and Werner, Thomas and Tin, Sergey
    and de Vries, Johannes G.}, year={2019}, pages={8012–8067} }'
  chicago: 'Stadler, Bernhard M., Christoph Wulf, Thomas Werner, Sergey Tin, and Johannes
    G. de Vries. “Catalytic Approaches to Monomers for Polymers Based on Renewables.”
    <i>ACS Catalysis</i> 9, no. 9 (2019): 8012–67. <a href="https://doi.org/10.1021/acscatal.9b01665">https://doi.org/10.1021/acscatal.9b01665</a>.'
  ieee: 'B. M. Stadler, C. Wulf, T. Werner, S. Tin, and J. G. de Vries, “Catalytic
    Approaches to Monomers for Polymers Based on Renewables,” <i>ACS Catalysis</i>,
    vol. 9, no. 9, pp. 8012–8067, 2019, doi: <a href="https://doi.org/10.1021/acscatal.9b01665">10.1021/acscatal.9b01665</a>.'
  mla: Stadler, Bernhard M., et al. “Catalytic Approaches to Monomers for Polymers
    Based on Renewables.” <i>ACS Catalysis</i>, vol. 9, no. 9, American Chemical Society
    (ACS), 2019, pp. 8012–67, doi:<a href="https://doi.org/10.1021/acscatal.9b01665">10.1021/acscatal.9b01665</a>.
  short: B.M. Stadler, C. Wulf, T. Werner, S. Tin, J.G. de Vries, ACS Catalysis 9
    (2019) 8012–8067.
date_created: 2023-01-22T20:42:48Z
date_updated: 2025-11-10T09:01:51Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acscatal.9b01665
intvolume: '         9'
issue: '9'
keyword:
- T4
- CSSD
language:
- iso: eng
page: 8012-8067
publication: ACS Catalysis
publication_identifier:
  issn:
  - 2155-5435
  - 2155-5435
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Catalytic Approaches to Monomers for Polymers Based on Renewables
type: journal_article
user_id: '89271'
volume: 9
year: '2019'
...
---
_id: '37965'
author:
- first_name: Aiga
  full_name: Grandane, Aiga
  last_name: Grandane
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Catrin
  full_name: Roolf, Catrin
  last_name: Roolf
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Hugo
  full_name: Murua Escobar, Hugo
  last_name: Murua Escobar
- first_name: Christian
  full_name: Junghanss, Christian
  last_name: Junghanss
- first_name: Edgars
  full_name: Suna, Edgars
  last_name: Suna
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: 'Grandane A, Longwitz L, Roolf C, et al. Intramolecular Base-Free Catalytic
    Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>.
    2019;84(3):1320-1329. doi:<a href="https://doi.org/10.1021/acs.joc.8b02789">10.1021/acs.joc.8b02789</a>'
  apa: 'Grandane, A., Longwitz, L., Roolf, C., Spannenberg, A., Murua Escobar, H.,
    Junghanss, C., Suna, E., &#38; Werner, T. (2019). Intramolecular Base-Free Catalytic
    Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>,
    <i>84</i>(3), 1320–1329. <a href="https://doi.org/10.1021/acs.joc.8b02789">https://doi.org/10.1021/acs.joc.8b02789</a>'
  bibtex: '@article{Grandane_Longwitz_Roolf_Spannenberg_Murua Escobar_Junghanss_Suna_Werner_2019,
    title={Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones},
    volume={84}, DOI={<a href="https://doi.org/10.1021/acs.joc.8b02789">10.1021/acs.joc.8b02789</a>},
    number={3}, journal={The Journal of Organic Chemistry}, publisher={American Chemical
    Society (ACS)}, author={Grandane, Aiga and Longwitz, Lars and Roolf, Catrin and
    Spannenberg, Anke and Murua Escobar, Hugo and Junghanss, Christian and Suna, Edgars
    and Werner, Thomas}, year={2019}, pages={1320–1329} }'
  chicago: 'Grandane, Aiga, Lars Longwitz, Catrin Roolf, Anke Spannenberg, Hugo Murua
    Escobar, Christian Junghanss, Edgars Suna, and Thomas Werner. “Intramolecular
    Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones.” <i>The Journal
    of Organic Chemistry</i> 84, no. 3 (2019): 1320–29. <a href="https://doi.org/10.1021/acs.joc.8b02789">https://doi.org/10.1021/acs.joc.8b02789</a>.'
  ieee: 'A. Grandane <i>et al.</i>, “Intramolecular Base-Free Catalytic Wittig Reaction:
    Synthesis of Benzoxepinones,” <i>The Journal of Organic Chemistry</i>, vol. 84,
    no. 3, pp. 1320–1329, 2019, doi: <a href="https://doi.org/10.1021/acs.joc.8b02789">10.1021/acs.joc.8b02789</a>.'
  mla: 'Grandane, Aiga, et al. “Intramolecular Base-Free Catalytic Wittig Reaction:
    Synthesis of Benzoxepinones.” <i>The Journal of Organic Chemistry</i>, vol. 84,
    no. 3, American Chemical Society (ACS), 2019, pp. 1320–29, doi:<a href="https://doi.org/10.1021/acs.joc.8b02789">10.1021/acs.joc.8b02789</a>.'
  short: A. Grandane, L. Longwitz, C. Roolf, A. Spannenberg, H. Murua Escobar, C.
    Junghanss, E. Suna, T. Werner, The Journal of Organic Chemistry 84 (2019) 1320–1329.
date_created: 2023-01-22T20:45:12Z
date_updated: 2025-11-10T09:10:18Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acs.joc.8b02789
extern: '1'
intvolume: '        84'
issue: '3'
keyword:
- T2
- T4
- CSSD
language:
- iso: eng
page: 1320-1329
publication: The Journal of Organic Chemistry
publication_identifier:
  issn:
  - 0022-3263
  - 1520-6904
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: 'Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones'
type: journal_article
user_id: '89271'
volume: 84
year: '2019'
...
---
_id: '62105'
author:
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Johannes
  full_name: Steinbauer, Johannes
  last_name: Steinbauer
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic
    System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.
    <i>ACS Catalysis</i>. 2018;8(1):665-672. doi:<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>
  apa: Longwitz, L., Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2018). Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions. <i>ACS Catalysis</i>, <i>8</i>(1), 665–672. <a href="https://doi.org/10.1021/acscatal.7b03367">https://doi.org/10.1021/acscatal.7b03367</a>
  bibtex: '@article{Longwitz_Steinbauer_Spannenberg_Werner_2018, title={Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions}, volume={8}, DOI={<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>},
    number={1}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)},
    author={Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner,
    Thomas}, year={2018}, pages={665–672} }'
  chicago: 'Longwitz, Lars, Johannes Steinbauer, Anke Spannenberg, and Thomas Werner.
    “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates
    under Mild Conditions.” <i>ACS Catalysis</i> 8, no. 1 (2018): 665–72. <a href="https://doi.org/10.1021/acscatal.7b03367">https://doi.org/10.1021/acscatal.7b03367</a>.'
  ieee: 'L. Longwitz, J. Steinbauer, A. Spannenberg, and T. Werner, “Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions,” <i>ACS Catalysis</i>, vol. 8, no. 1, pp. 665–672, 2018, doi: <a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>.'
  mla: Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of
    Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i>, vol.
    8, no. 1, American Chemical Society (ACS), 2018, pp. 665–72, doi:<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>.
  short: L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2018)
    665–672.
date_created: 2025-11-05T15:47:56Z
date_updated: 2025-11-10T09:05:26Z
department:
- _id: '35'
- _id: '2'
doi: 10.1021/acscatal.7b03367
intvolume: '         8'
issue: '1'
keyword:
- T1
- T3
- T4
- CSSD
language:
- iso: eng
page: 665-672
publication: ACS Catalysis
publication_identifier:
  issn:
  - 2155-5435
  - 2155-5435
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates
  under Mild Conditions
type: journal_article
user_id: '89271'
volume: 8
year: '2018'
...
---
_id: '37970'
author:
- first_name: Lars
  full_name: Longwitz, Lars
  last_name: Longwitz
- first_name: Johannes
  full_name: Steinbauer, Johannes
  last_name: Steinbauer
- first_name: Anke
  full_name: Spannenberg, Anke
  last_name: Spannenberg
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: https://orcid.org/0000-0001-9025-3244
citation:
  ama: Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic
    System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.
    <i>ACS Catalysis</i>. 2017;8(1):665-672. doi:<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>
  apa: Longwitz, L., Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions. <i>ACS Catalysis</i>, <i>8</i>(1), 665–672. <a href="https://doi.org/10.1021/acscatal.7b03367">https://doi.org/10.1021/acscatal.7b03367</a>
  bibtex: '@article{Longwitz_Steinbauer_Spannenberg_Werner_2017, title={Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions}, volume={8}, DOI={<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>},
    number={1}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)},
    author={Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner,
    Thomas}, year={2017}, pages={665–672} }'
  chicago: 'Longwitz, Lars, Johannes Steinbauer, Anke Spannenberg, and Thomas Werner.
    “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates
    under Mild Conditions.” <i>ACS Catalysis</i> 8, no. 1 (2017): 665–72. <a href="https://doi.org/10.1021/acscatal.7b03367">https://doi.org/10.1021/acscatal.7b03367</a>.'
  ieee: 'L. Longwitz, J. Steinbauer, A. Spannenberg, and T. Werner, “Calcium-Based
    Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild
    Conditions,” <i>ACS Catalysis</i>, vol. 8, no. 1, pp. 665–672, 2017, doi: <a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>.'
  mla: Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of
    Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i>, vol.
    8, no. 1, American Chemical Society (ACS), 2017, pp. 665–72, doi:<a href="https://doi.org/10.1021/acscatal.7b03367">10.1021/acscatal.7b03367</a>.
  short: L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2017)
    665–672.
date_created: 2023-01-22T20:47:19Z
date_updated: 2025-11-06T08:38:07Z
department:
- _id: '35'
- _id: '2'
- _id: '657'
doi: 10.1021/acscatal.7b03367
extern: '1'
intvolume: '         8'
issue: '1'
keyword:
- T1
- T3
- T4
language:
- iso: eng
page: 665-672
publication: ACS Catalysis
publication_identifier:
  issn:
  - 2155-5435
  - 2155-5435
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates
  under Mild Conditions
type: journal_article
user_id: '89271'
volume: 8
year: '2017'
...