Efficient electroorganic synthesis of 2,3,6,7,10,11-hexahydroxytriphenylene derivatives

Carolin Regenbrecht and Siegfried R. Waldvogel
Beilstein J. Org. Chem. 2012, 8, 1721–1724. https://doi.org/10.3762/bjoc.8.196

Supporting Information

Supporting Information File 1: Characterization data and spectra of synthesized compounds.
Format: PDF Size: 828.0 KB Download

Cite the Following Article

Efficient electroorganic synthesis of 2,3,6,7,10,11-hexahydroxytriphenylene derivatives
Carolin Regenbrecht and Siegfried R. Waldvogel
Beilstein J. Org. Chem. 2012, 8, 1721–1724. https://doi.org/10.3762/bjoc.8.196

How to Cite

Regenbrecht, C.; Waldvogel, S. R. Beilstein J. Org. Chem. 2012, 8, 1721–1724. doi:10.3762/bjoc.8.196

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Knapp, J. G.; Wang, X.; Rosen, A. S.; Wang, X.; Gong, X.; Schneider, M.; Elkin, T.; Kirlikovali, K. O.; Fairley, M.; Krzyaniak, M. D.; Wasielewski, M. R.; Gianneschi, N. C.; Snurr, R. Q.; Farha, O. K. Evidence of a Uranium-Paddlewheel Node in a Catecholate-Based Metal-Organic Framework. Angewandte Chemie (International ed. in English) 2023, 62, e202305526. doi:10.1002/anie.202305526
  • Knapp, J. G.; Wang, X.; Rosen, A. S.; Wang, X.; Gong, X.; Schneider, M.; Elkin, T.; Kirlikovali, K. O.; Fairley, M.; Krzyaniak, M. D.; Wasielewski, M. R.; Gianneschi, N. C.; Snurr, R. Q.; Farha, O. K. Evidence of a Uranium‐Paddlewheel Node in a Catecholate‐Based Metal–Organic Framework. Angewandte Chemie 2023, 135. doi:10.1002/ange.202305526
  • Babujohn, N. A.; Eluri, A.; Nabeela, V. One pot synthesis of crystalline covalent organic polymers with tunable pores for the removal of gold and toxic organic pollutants. Chemical Engineering Journal 2023, 464, 142459. doi:10.1016/j.cej.2023.142459
  • Li, Z.; Shuai, B.; Ma, C.; Fang, P.; Mei, T. Nickel‐Catalyzed Electroreductive Syntheses of Triphenylenes Using ortho‐Dihalobenzene‐Derived Benzynes. Chinese Journal of Chemistry 2022, 40, 2335–2344. doi:10.1002/cjoc.202200245
  • Sato, E.; Niki, Y.; Mitsudo, K.; Suga, S. Electro-oxidative Trimerization of 1,2-Dimethoxybenzene: Reductive Workup Strategy and Alternating Current Electrolysis to Peel off the Precipitated Radical Cation Ion Pair. Chemistry Letters 2022, 51, 629–632. doi:10.1246/cl.220112
  • Selt, M.; Waldvogel, S. R. 9 Anodic Arylation Reactions. Electrochemistry in Organic Synthesis; Georg Thieme Verlag KG, 2022. doi:10.1055/sos-sd-236-00167
  • Nakamura, Y.; Sato, Y.; Shida, N.; Atobe, M. Electrochemical Trimerization of Catechol to 2,3,6,7,10,11-Hexahydroxytriphenylene Using a Flow Microreactor. Electrochemistry 2021, 89, 395–399. doi:10.5796/electrochemistry.21-00053
  • Dahms, B.; Kohlpaintner, P. J.; Wiebe, A.; Breinbauer, R.; Schollmeyer, D.; Waldvogel, S. R. Selective Formation of 4,4′-Biphenols by Anodic Dehydrogenative Cross- and Homo-Coupling Reaction. Chemistry (Weinheim an der Bergstrasse, Germany) 2019, 25, 2713–2716. doi:10.1002/chem.201805737
  • Waldvogel, S. R.; Lips, S.; Selt, M.; Riehl, B.; Kampf, C. J. Electrochemical Arylation Reaction. Chemical reviews 2018, 118, 6706–6765. doi:10.1021/acs.chemrev.8b00233
  • Wiebe, A.; Gieshoff, T.; Möhle, S.; Rodrigo, E.; Zirbes, M.; Waldvogel, S. R. Electrifying Organic Synthesis. Angewandte Chemie (International ed. in English) 2018, 57, 5594–5619. doi:10.1002/anie.201711060
  • Wiebe, A.; Gieshoff, T.; Möhle, S.; Rodrigo, E.; Zirbes, M.; Waldvogel, S. R. Elektrifizierung der organischen Synthese. Angewandte Chemie 2018, 130, 5694–5721. doi:10.1002/ange.201711060
  • Tang, S.; Liu, Y.; Lei, A. Electrochemical Oxidative Cross-coupling with Hydrogen Evolution: A Green and Sustainable Way for Bond Formation. Chem 2018, 4, 27–45. doi:10.1016/j.chempr.2017.10.001
Other Beilstein-Institut Open Science Activities