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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_067fa7a6d043b14968b8dca94aa94e37
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-608
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D301-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-32
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-608
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
filingDate 2000-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c073c010cb7fe324047c6a6fbde65034
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2557ce4eebedd58af8813f068ee0859
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3247508aee73e179c2154dbe5c65857
publicationDate 2000-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1048643-A1
titleOfInvention Process for the preparation of chiral epoxides
abstract The invention describes novel malonates and a process for using saidnmalonates for the preparation of chiral epoxides of formulan nhaving a cyclanic (1R) configuration, the group in position 2 having a transconfigurationnand the epoxy group having a cis-configuration with respect to thensubstituent in position 1 and wherein R is an alkyl group from C 1 to C 4 , linear ornbranched, and R 1 is an alkyl or an alkenyl group from C 2 to C 8 , linear or branched. Thenabove process comprises the rearrangement of malonate (VII) to malonate (VI) and thendecarboxylation reaction ofn ninto an ester of formulan nfollowed by the stereoselective epoxidation of the thus-obtained compound.
priorityDate 1999-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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