http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-419468-B

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filingDate 1996-08-29^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-01-21^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4881450c12ec11a1cb1802266ffac8e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ae592202504f9a021fc0a12a41047ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4566c914ec8c3f44dc1f0e2428f03a77
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0f7187b50c3f8538b62735d8168466f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2573587c3232c4d6018c1ba46d0f6e4
publicationDate 2001-01-21^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-419468-B
titleOfInvention Phenyloxazolidinones having a C-C bond to 4-8 membered heterocyclic rings
abstract A compound of the formula (I), or pharmaceutical acceptable salts thereof wherein X is NR1, s(o)g, or O; R1 is H, C1-6 alky1 optionally substituted with one or more OH, CN, or halo, or R1 is -(CH2)h-ary1, -COR1-1, -COOR1-2,-CO-(CH2)h-COR1-1, C1-6 alky1 sulfony1, -SO2-(CH2)h-ary1, or -(CO)I-Het, R2 is H, C1-6 alky1, -(CH2)h-ary1, or halo; R3 and R4 are the same or different and are H or halo; R5 is H,C1-12 alky1 optionally substituted with one or more halo, C3-12 cycloalky1, C1-6alkoxy. The compounds are useful antimicrobial agents.
priorityDate 1995-09-01^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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