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Transition-metal-free solid phase synthesis of 1,2-disubstituted 4-quinolones via the regiospecific synthesis of enaminones
Herein, the transition-metal-free economical solid phase synthesis of 1,2-disubstituted 4-quinolones has been developed via the novel regiospecific synthesis of enaminones. Notably, a wide range of enaminones were synthesized via a silica-supported solid-phase reaction in good to excellent yields. T...
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Published in: | RSC advances 2016, Vol.6 (14), p.11528-11535 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Herein, the transition-metal-free economical solid phase synthesis of 1,2-disubstituted 4-quinolones has been developed
via
the novel regiospecific synthesis of enaminones. Notably, a wide range of enaminones were synthesized
via
a silica-supported solid-phase reaction in good to excellent yields. The transformation of enaminones to 1,2-disubstituted 4-quinolones and
N
-methyl-2-aryl-4-quinolone alkaloid was achieved in high yield
via
an alumina-supported solid phase reaction. In addition, all the synthesized compounds were isolated directly in their pure form from the reaction mixture using an easy workup procedure. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C5RA21421A |