Copper-Catalyzed Remote C–H Arylation of Polycyclic Aromatic Hydrocarbons (PAHs)

Submitting author affiliation:
Sichuan University, Chengdu, China

Beilstein Arch. 2020, 202011. https://doi.org/10.3762/bxiv.2020.11.v1

Published 20 Jan 2020

Preprint
cc-by Logo

Abstract

The regioselective C–H arylation of substituted polycyclic aromatic hydrocarbons (PAHs) is a desired but challenging task. Herein, a copper-catalyzed C7–H arylation of 1-naphthamides has been developed by using aryliodonium salts as arylating reagents. This protocol does not need to use precious metal catalysts and can tolerate wide functional groups. Under standard conditions, the remote C–H arylation of other PAHs including phenanthrene-9-carboxamide, pyrene-1-carboxamide and fluoranthene-3-carboxamide has also accomplished, which provides an opportunity for the development of diverse organic optoelectronic materials.

Keywords: Copper-Catalyzed; C–H Arylation; Polycyclic Aromatic Hydrocarbons (PAHs); Non-precious Metal Catalyst; Regioselectivity

Supporting Information

Format: PDF Size: 6.3 MB   Download

How to Cite

When a peer-reviewed version of this preprint is available, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Luo, A.; Zhang, M.; Fu, Z.; Lan, J.; Wu, D.; You, J. Beilstein Arch. 2020, 202011. doi:10.3762/bxiv.2020.11.v1

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.

OTHER BEILSTEIN-INSTITUT OPEN SCIENCE ACTIVITIES