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2 ratio was increased from 1:1 to 2:1 to limit reductive de-iodination.
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Initial synthetic attempts using formic acetic anhydride as the CO source produced compound 3, albeit in much lower yield, with predominant formation of the des-iodoquinolone.
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Initial synthetic attempts using formic acetic anhydride as the CO source produced compound 3, albeit in much lower yield, with predominant formation of the des-iodoquinolone.
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Because of a bias against compounds containing two carboxylic acid functional groups, further investigation of the scaffold represented by 8 {6} was not pursued in spite of its improved PHD inhibitory activity.
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Because of a bias against compounds containing two carboxylic acid functional groups, further investigation of the scaffold represented by 8 {6} was not pursued in spite of its improved PHD inhibitory activity.
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Molecular modeling studies were performed as described in ref 7f.
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Molecular modeling studies were performed as described in ref 7f.
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