http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200706543-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K49-14
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filingDate 2005-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6e783f7da45d5c2fb4f2bdbe294aca5
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publicationDate 2007-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200706543-A
titleOfInvention A convenient method for the preparation of no-carrier-added O-(2-[18F]fluoroethyl)-L-tyrosine
abstract This is a new precursor and new method for the synthesis of no-carrier-added O-(2-[18F]fluoroethyl)-L-Tyrosine which has been proved a suitable PET (position emission tomography) probe for tumor diagnosis imaging. The preparation of the title compound starts from precursors with the chemical structures as in Figure 1, wherein R1 is a protective group for the carboxyl functional group, R2 is a protective group for the amino group, and R3 acts as a leaving group. R1 represents an arylalkyl group, R2 represents a carboxyl group, and R represents a p-tosyloxy, methane sulfonyloxy or trifluoromethane sulfonyloxy or bromine. The invention includes a method for the syntheses of new precursors with the chemical structures as in Figure 1.
priorityDate 2005-08-04-04:00^^<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: 25.