Please use this identifier to cite or link to this item:
http://hdl.handle.net/2067/52733
Title: | Palladium-catalyzed synthesis of 6-aryl dopamine derivatives | Authors: | Calcaterra Andrea Fernández García Santiago Marrone Federico Bernini, Roberta Fabrizi Giancarlo Goggiamani Antonella Iazzetti Antonia |
Journal: | CATALYSTS | Issue Date: | 2024 | Abstract: | Dopamine is a key neurotransmitter involved in a series of biologically relevant processes and its derivatives have sparked significant interest as intriguing synthetic targets. This class of compounds is indeed not only considerable for the potential biological activities but is also promising for diverse applications in material science. In light of this, our research was focused on the synthesis of 6-aryldopamine derivatives starting from 4-(2-aminoethyl)phenol through a sequential protocol, whose main steps are hydroxylation, halogenation, and Suzuki cross-coupling. Our method demonstrated versatility, efficiency, and compatibility with various functional groups, including aldehydes, ketones, esters, ethers, and fluorine. |
URI: | http://hdl.handle.net/2067/52733 | ISSN: | 2073-4344 | DOI: | 10.3390/catal14070401 | Rights: | Attribution-NonCommercial-NoDerivatives 4.0 International |
Appears in Collections: | A1. Articolo in rivista |
Files in This Item:
File | Description | Size | Format | Existing users please |
---|---|---|---|---|
Catalysts 2024_14_7_401 415.pdf | 791.99 kB | Adobe PDF | Request a copy |
SCOPUSTM
Citations
1
Last Week
0
0
Last month
checked on Feb 2, 2025
Page view(s)
9
checked on Feb 5, 2025
Google ScholarTM
Check
Altmetric
This item is licensed under a Creative Commons License