AlCl3-mediated hydroarylationheteroarylation in a single pot: a direct access to densely functionalized olefins of pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of in vitro/in vivo and docking study. See DOI: 10.1039/c3cc42840k
An unprecedented AlCl 3 -mediated method has been developed involving aromatic CH bond addition to an alkyne and heteroarylation of an arene in a single pot leading to densely functionalized novel olefins, e.g. 2-(2,2-diarylvinyl)-3-arylquinoxalines, as potential inhibitors of sirtuins. Novel 2-viny...
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Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An unprecedented AlCl
3
-mediated method has been developed involving aromatic CH bond addition to an alkyne and heteroarylation of an arene in a single pot leading to densely functionalized novel olefins,
e.g.
2-(2,2-diarylvinyl)-3-arylquinoxalines, as potential inhibitors of sirtuins.
Novel 2-vinyl-3-arylquinoxalines are synthesized
via
an AlCl
3
-mediated hydroarylationheteroarylation reaction in a single pot. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c3cc42840k |