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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-01
filingDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1989-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aedc744329e13a653c32f238027562d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75a46a2ff23b40de624f5d456db12651
publicationDate 1989-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4857544-A
titleOfInvention 27-Halo derivatives of LL-F28249 compounds
abstract The present invention relates to novel derivatives of LL-F28249 compounds wherein the pendent C(26,27) olefinic group at C(25) is converted into a 27-bromo or 27-chloro-26-methylene group. The 27-bromo compounds are derived by reacting the LL-F28249 compounds or 5-0-trisubstituted silyl LL-F28249 compounds with N-bromoacetamide or N-bromosuccinimide in aqueous acetone, followed by desilylation for silylated LL-F28249 intermediates. The 27-chloro compounds are prepared by reacting LL-F28249 compounds with N-chlorosuccinimide in methanol. These novel halo compounds have anthelmintic, ectoparasitic, insecticidal, nematicidal and acaricidal activity and are also useful intermediates for the preparation of other novel biologically active compounds. Compositions containing the present compounds as active ingredients thereof are presented.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5106994-A
priorityDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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