1,4-Dithianes: attractive C2-building blocks for the synthesis of complex molecular architectures

Bram Ryckaert, Ellen Demeyere, Frederick Degroote, Hilde Janssens and Johan M. Winne
Beilstein J. Org. Chem. 2023, 19, 115–132. https://doi.org/10.3762/bjoc.19.12

Cite the Following Article

1,4-Dithianes: attractive C2-building blocks for the synthesis of complex molecular architectures
Bram Ryckaert, Ellen Demeyere, Frederick Degroote, Hilde Janssens and Johan M. Winne
Beilstein J. Org. Chem. 2023, 19, 115–132. https://doi.org/10.3762/bjoc.19.12

How to Cite

Ryckaert, B.; Demeyere, E.; Degroote, F.; Janssens, H.; Winne, J. M. Beilstein J. Org. Chem. 2023, 19, 115–132. doi:10.3762/bjoc.19.12

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.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 10.8 MB Download

Citations to This Article

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

Scholarly Works

  • Qatran Al-Khdhairawi, A. A.; Yuan, T.; Van Hecke, K.; Winne, J. M. Dearomative (3 + 2) Cycloaddition of Indoles for the Stereoselective Assembly of Fully Functionalized Cyclopentanoids. Organic letters 2024, 26, 4077–4081. doi:10.1021/acs.orglett.4c01139
  • Degroote, F.; Denoo, B.; Ryckaert, B.; Callebaut, B.; Van Hecke, K.; Hullaert, J.; Winne, J. M. Dithioallyl cation (3 + 2) cycloadditions under aprotic reaction conditions: rapid access to spiro-fused cyclopentane scaffolds. Organic & biomolecular chemistry 2023, 21, 8117–8124. doi:10.1039/d3ob01273e
  • Ryckaert, B.; Hullaert, J.; Van Hecke, K.; Winne, J. M. Dithioallyl Cations in Stereoselective Dearomative (3 + 2) Cycloadditions of Benzofurans: Mechanism and Synthetic Applications. The Journal of organic chemistry 2023, 88, 14504–14514. doi:10.1021/acs.joc.3c01546
Other Beilstein-Institut Open Science Activities