AI Article Synopsis
- A new method has been developed to create 6-aminoquinoline derivatives by combining three specific chemical reactions: a tandem Povarov reaction, oxidation of dihydroquinoline, and reduction of imines.
- This synthesis leads to the formation of both symmetrical and unsymmetrical tetraarylpyrido[2,3-g]quinolines.
- These new compounds could be beneficial for applications in organic electronics.
Article Abstract
A new strategy is reported for the synthesis of 6-aminoquinoline derivatives via a tandem Povarov reaction, dihydroquinoline oxidation, and imine reduction. These products allow access to symmetrical as well as unsymmetrical tetraarylpyrido[2,3-g]quinolines, potentially useful organic electronics.
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| http://dx.doi.org/10.1021/ol4016354 | DOI Listing |
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