Substitution reactions in the acenaphthene analog of quino[7,8-h]quinoline and an unusual synthesis of the corresponding acenaphthylenes by tele-elimination

Ekaterina V. Kolupaeva, Narek A. Dzhangiryan, Alexander F. Pozharskii, Oleg P. Demidov and Valery A. Ozeryanskii
Beilstein J. Org. Chem. 2024, 20, 243–253. https://doi.org/10.3762/bjoc.20.24

Supporting Information

CCDC 2294253 (for 2(5)·(4,6-dichlororesorcinol)), 2294254 (for HBF4), 2294255 (for HBF4), 2294256 (for 5), 2294257 (for HCl·2H2O) contain supporting crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Center via https://www.ccdc.cam.ac.uk/data_request/cif.

Supporting Information File 1: Additional experimental and XRD information, synthetic procedures, copies of NMR spectral data for new compounds.
Format: PDF Size: 3.3 MB Download

Cite the Following Article

Substitution reactions in the acenaphthene analog of quino[7,8-h]quinoline and an unusual synthesis of the corresponding acenaphthylenes by tele-elimination
Ekaterina V. Kolupaeva, Narek A. Dzhangiryan, Alexander F. Pozharskii, Oleg P. Demidov and Valery A. Ozeryanskii
Beilstein J. Org. Chem. 2024, 20, 243–253. https://doi.org/10.3762/bjoc.20.24

How to Cite

Kolupaeva, E. V.; Dzhangiryan, N. A.; Pozharskii, A. F.; Demidov, O. P.; Ozeryanskii, V. A. Beilstein J. Org. Chem. 2024, 20, 243–253. doi:10.3762/bjoc.20.24

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: 8.0 MB Download
Other Beilstein-Institut Open Science Activities