http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0203381-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-94
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C61-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-94
filingDate 2000-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94540714b7e8455cec29614bd54c63cd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d543be8396266c1455360c3fbe3ddfdb
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_305e9b6238b292920e79c464ed4bb105
publicationDate 2003-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0203381-A2
titleOfInvention 5-halo-4-fluoro-4,7,7-trimethyl-3-oxabicyclo [4.1.0] heptan-2-one for the preparation and use of cyclopropanecarboxylic acids.
abstract The present invention relates to compounds of formula I wherein Hal is chlorine, bromine or iodine. The compounds can be used as intermediates in the preparation of pyrethroid derivatives. The present invention also relates to a process for the preparation of compounds of formula I and to processes for the preparation of apiretroids. ) wherein R is an alcohol derived from a pyrethroid group. SHE
priorityDate 1999-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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