An Improved Synthesis of <i>N</i>-Trifluoroacetyl-<scp>l</scp>-daunosamine

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<jats:title>Abstract</jats:title> <jats:p>A process which can afford a large quantity of the title compound was explored by modifying the Horton’s original route. The developed process features highly stereoselective reduction of the oxime with sodium dihydrobis(2-methoxyethanolato)aluminate(1-) and efficient dehydrobromination with 1,8-diazabicyclo[5.4.0]undec-7-ene.</jats:p>

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