Synlett 2013; 24(3): 359-362
DOI: 10.1055/s-0032-1318003
letter
© Georg Thieme Verlag Stuttgart · New York

Suzuki–Miyaura Reactions of 2,7-Dichloro-1,8-naphthyridine

Peter Ehlers
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany, Fax: +49(381)4986412   Email: peter.langer@uni-rostock.de
b   Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
,
Andranik Petrosyan
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany, Fax: +49(381)4986412   Email: peter.langer@uni-rostock.de
b   Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
c   Faculty of Chemistry, Yerevan State University, Alex Manoogian 1, 0025 Yerevan, Armenia
,
Tariel V. Ghochikyan
c   Faculty of Chemistry, Yerevan State University, Alex Manoogian 1, 0025 Yerevan, Armenia
,
Ashot S. Saghyan
c   Faculty of Chemistry, Yerevan State University, Alex Manoogian 1, 0025 Yerevan, Armenia
d   Scientific and Production Center ‘Armbiotechnology’ of NAS RA, Gyurjyan str. 14, 0056 Yerevan, Armenia
,
Antje Neubauer
e   Institut für Physik, Universität Rostock, Universitätsplatz 3, 18051 Rostock, Germany
,
Stefan Lochbrunner
e   Institut für Physik, Universität Rostock, Universitätsplatz 3, 18051 Rostock, Germany
,
Peter Langer*
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany, Fax: +49(381)4986412   Email: peter.langer@uni-rostock.de
b   Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
› Author Affiliations
Further Information

Publication History

Received: 06 December 2012

Accepted: 17 December 2012

Publication Date:
10 January 2013 (online)


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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.

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