Supporting Information
| Supporting Information File 1: Experimental details, synthetic procedures, single crystal X-ray data for 1, detailed theoretical calculations, and analytical data for the compounds. | ||
| Format: PDF | Size: 1.6 MB | Download |
Cite the Following Article
One-pot synthesis of dicyclopenta-fused peropyrene via a fourfold alkyne annulation
Ji Ma, Yubin Fu, Junzhi Liu and Xinliang Feng
Beilstein J. Org. Chem. 2020, 16, 791–797.
https://doi.org/10.3762/bjoc.16.72
How to Cite
Ma, J.; Fu, Y.; Liu, J.; Feng, X. Beilstein J. Org. Chem. 2020, 16, 791–797. doi:10.3762/bjoc.16.72
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: 277.1 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Sharma, P. K.; Babbar, A.; Mallick, D.; Das, S. Constructing 1-Ethoxyphenanthro[9,10-e]acephenanthrylene for the Synthesis of a Polyaromatic Hydrocarbon Containing a Formal Azulene Unit. The Journal of organic chemistry 2023, 88, 5473–5482. doi:10.1021/acs.joc.2c03103
- Chen, P.-T.; Yu, C.-L.; Shen, M.-H.; Cheng, M.-J.; Wu, Y.-T.; Hsu, H.-F. Highly Substituted Acephenanthrylenes and Their π-Extended Derivatives: Syntheses, Structural Analyses, and Properties. Organic letters 2022, 24, 4778–4782. doi:10.1021/acs.orglett.2c01778
- Ajayakumar, M. R.; Di Giovannantonio, M.; Pignedoli, C. A.; Yang, L.; Ruffieux, P.; Ma, J.; Fasel, R.; Feng, X. On‐surface synthesis of porous graphene nanoribbons containing nonplanar [14]annulene pores. Journal of Polymer Science 2022, 60, 1912–1917. doi:10.1002/pol.20220003
- Werner, S.; Vollgraff, T.; Sundermeyer, J. Tetrasubstituted Peropyrenes Formed by Reductive Aromatization: Synthesis, Functionalization and Characterization. Chemistry (Weinheim an der Bergstrasse, Germany) 2021, 27, 11065–11075. doi:10.1002/chem.202101101
