http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-445381-A1

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filingDate 1976-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-445381-A1
titleOfInvention A PROCEDURE OF ASYMMETRICAL CONVERTING 2-DEUTERO-3-FLUOR-1-ALANINE INTO THE CORRESPONDING ISOMER D.
abstract 2-Deutero-3-fluoro-L-alanine is converted into its D-isomer in an asymmetrical manner. In this process, the L-isomer is reacted with sodium nitrite to give the corresponding L-2-deutero-2-halo-3-fluoro-propionic acid in solution in an aqueous hydrohalic acid. This L-2-deutero-2-halo-3-fluoropropionic acid is then reacted either with ammonia or with sodium azide with replacement of the 2-halogen substituent by a 2-azido group and subsequent catalytic hydrogenation to give 2-deutero-3-fluoro-D-alanine. 2-Deutero-3-fluoro-L-alanine can be converted into pharmaceutically acceptable salts. The resulting compound can be used for inhibition of the growth of Gram-positive and Gram-negative pathogenic bacteria.
priorityDate 1975-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 27.