Abstract
[reaction: see text]. A highly regioselective Friedländer reaction is described. By introduction of a phosphonate group at one of the alpha-carbons of a ketone, regioselectivity can be perfectly controlled.
MeSH terms
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Carbon / chemistry
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Ketones / chemistry
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Magnetic Resonance Spectroscopy
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Methanol / chemistry
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Models, Chemical
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Naphthyridines / chemical synthesis*
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Phosphates / chemistry
Substances
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Ketones
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Naphthyridines
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Phosphates
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Carbon
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Methanol