Abstract
A new synthetic approach to 3-aryl isoquinolines, based on the Pd-catalyzed Suzuki cross-coupling reaction, is reported. The described procedure represents an efficient method to prepare 3-aryl isoquinolines by reaction of a preformed 3-chloro isoquinoline with a phenylboronic acid, especially when the nitrogen atom is positively charged.
Keywords: Suzuki cross-coupling, Pd catalysis, 3-aryl isoquinolines
Letters in Organic Chemistry
Title: New Synthesis of 3-Aryl Isoquinolines by Pd-Catalyzed Suzuki Cross-Coupling
Volume: 4 Issue: 2
Author(s): Marco Franceschin, Stefano Frasca, Antonello Alvino and Armandodoriano Bianco
Affiliation:
Keywords: Suzuki cross-coupling, Pd catalysis, 3-aryl isoquinolines
Abstract: A new synthetic approach to 3-aryl isoquinolines, based on the Pd-catalyzed Suzuki cross-coupling reaction, is reported. The described procedure represents an efficient method to prepare 3-aryl isoquinolines by reaction of a preformed 3-chloro isoquinoline with a phenylboronic acid, especially when the nitrogen atom is positively charged.
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Cite this article as:
Franceschin Marco, Frasca Stefano, Alvino Antonello and Bianco Armandodoriano, New Synthesis of 3-Aryl Isoquinolines by Pd-Catalyzed Suzuki Cross-Coupling, Letters in Organic Chemistry 2007; 4(2) . https://dx.doi.org/10.2174/157017807780414217
DOI https://dx.doi.org/10.2174/157017807780414217 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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