Rapid construction of tricyclic tetrahydrocyclopenta[4,5]pyrrolo[2,3-b]pyridine via isocyanide-based multicomponent reaction

Xiu-Yu Chen, Ying Han, Jing Sun and Chao-Guo Yan
Beilstein J. Org. Chem. 2024, 20, 1436–1443. https://doi.org/10.3762/bjoc.20.126

Supporting Information

The crystallographic data of the compounds 4a (CCDC 2346135) and 6g (CCDC 2346136) have been deposited at the Cambridge Crystallographic Database Center (http://www.ccdc.cam.ac.uk).

Supporting Information File 1: Characterization data and 1H NMR, 13C NMR, and HRMS spectra of compounds.
Format: PDF Size: 6.1 MB Download

Cite the Following Article

Rapid construction of tricyclic tetrahydrocyclopenta[4,5]pyrrolo[2,3-b]pyridine via isocyanide-based multicomponent reaction
Xiu-Yu Chen, Ying Han, Jing Sun and Chao-Guo Yan
Beilstein J. Org. Chem. 2024, 20, 1436–1443. https://doi.org/10.3762/bjoc.20.126

How to Cite

Chen, X.-Y.; Han, Y.; Sun, J.; Yan, C.-G. Beilstein J. Org. Chem. 2024, 20, 1436–1443. doi:10.3762/bjoc.20.126

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: 7.5 MB Download

Citations to This Article

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

Scholarly Works

  • Norouzi, M.; Nazeri, M. T.; Shaabani, A.; Notash, B. Synthesis of pyrrole-fused dibenzoxazepine/dibenzothiazepine/triazolobenzodiazepine derivatives via isocyanide-based multicomponent reactions. Beilstein journal of organic chemistry 2024, 20, 2870–2882. doi:10.3762/bjoc.20.241
  • Liu, D.-M.; Zhan, S.-C.; Fang, R.-J.; Sun, J.; Yan, C.-G. Selective Synthesis of Dihydro- and Dehydrogenated Spirocyclopenta[b]indoles via Acid-modulated [3+2] Cycloaddition Reaction. Journal of Molecular Structure 2024, 140792. doi:10.1016/j.molstruc.2024.140792
Other Beilstein-Institut Open Science Activities