Supporting Information
| Supporting Information File 1: Experimental details, details on electrochemical characterization, 1H and 13C NMR spectra of compounds 4b,d–f, UV–vis spectrum and CV of 4b, as well as full crystal structure descriptions. | ||
| Format: PDF | Size: 1.4 MB | Download |
| Supporting Information File 2: Zip archive containing X-ray crystallographic data for 4a (CCDC 987551), 4b (CCDC 1049639), 4d (CCDC 1049638) and 4e (CCDC 1049637). | ||
| Format: ZIP | Size: 1.3 MB | Download |
Cite the Following Article
Tuning of tetrathiafulvalene properties: versatile synthesis of N-arylated monopyrrolotetrathiafulvalenes via Ullmann-type coupling reactions
Vladimir A. Azov, Diana Janott, Dirk Schlüter and Matthias Zeller
Beilstein J. Org. Chem. 2015, 11, 860–868.
https://doi.org/10.3762/bjoc.11.96
How to Cite
Azov, V. A.; Janott, D.; Schlüter, D.; Zeller, M. Beilstein J. Org. Chem. 2015, 11, 860–868. doi:10.3762/bjoc.11.96
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- Schlüter, D.; Korsching, K. R.; Azov, V. A. Lower-Rim-Modified Calix[4]arene-Pyrrolotetrathiafulvalene Molecular Tweezers. European Journal of Organic Chemistry 2021, 2021, 4469–4476. doi:10.1002/ejoc.202100676
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- Aitken, R. A.; Dragomir, G.-I. Five-Membered Ring Systems. Progress in Heterocyclic Chemistry; Elsevier, 2016; pp 341–359. doi:10.1016/b978-0-08-100755-6.00010-7
- Azov, V. A.; Janott, D.; Schlueter, D.; Zeller, M. Tuning of Tetrathiafulvalene Properties: Versatile Synthesis of N‐Arylated Monopyrrolotetrathiafulvalenes via Ullmann‐Type Coupling Reactions. ChemInform 2015, 46. doi:10.1002/chin.201529167
