Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
The compounds 6-(pyrrol-2-yl)-2,2‘-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting str...
Main Authors: | Matthias Böttger, Björn Wiegmann, Steffen Schaumburg, Peter G. Jones, Wolfgang Kowalsky, Hans-Hermann Johannes |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2012-07-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.8.116 |
Similar Items
-
An Efficient Synthesis of Aryl-Substituted Pyrroles by the Suzuki–Miyaura Coupling Reaction of SEM-Protected Pyrroles
by: Keli Cui, et al.
Published: (2019-04-01) -
Free-radical cyclization approach to polyheterocycles containing pyrrole and pyridine rings
by: Ivan P. Mosiagin, et al.
Published: (2021-06-01) -
Towards a Metal-catalyzed Annulation Route to Pyridines and N-Hydroxy Pyrroles
by: Whitmore, Kenneth M.
Published: (2012) -
Towards a Metal-catalyzed Annulation Route to Pyridines and N-Hydroxy Pyrroles
by: Whitmore, Kenneth M.
Published: (2012) -
Towards a Metal-catalyzed Annulation Route to Pyridines and N-Hydroxy Pyrroles
by: Whitmore, Kenneth M.
Published: (2012)