Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2013; 24(3): 359-362
DOI: 10.1055/s-0032-1318003
DOI: 10.1055/s-0032-1318003
letter
Suzuki–Miyaura Reactions of 2,7-Dichloro-1,8-naphthyridine
Further Information
Publication History
Received: 06 December 2012
Accepted: 17 December 2012
Publication Date:
10 January 2013 (online)


Abstract
2,7-Diaryl- and 2,7-dialkenyl-1,8-naphthyridines were prepared in high yields by Suzuki–Miyaura reactions of 2,7-dichloro-1,8-naphthyridines. While most of the products proved to be not or only weakly fluorescent, we observed a strong fluorescence in case of 2,7-bis(4-methoxyphenyl)-1,8-naphthyridine containing two electron-donating aryl groups.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synlett.
- Supporting Information