http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20070078998-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-18
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C61-13
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C61-135
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C61-13
filingDate 2007-01-29^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f21eb18143327cb944bd7e3873bc41c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a04c14d9481ad6d29b4cdd514b3aade
publicationDate 2007-08-03^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20070078998-A
titleOfInvention Bicyclo [4.3.0] nonane-3 (4), 7 (8) -dicarboxylic acid and preparation method thereof
abstract The present invention relates to a compound bicyclo [4.3.0] nonane-3 (4), 7 (8) -dicarboxylic acid and a process for preparing the same, wherein bicyclo [4,3,0] nona-3,7 In the presence of a transition metal compound of Group 8 of the Periodic Table of the Periodic Table including complex-bound organophosphorus compounds and an excess of organophosphorus compounds, at a temperature of 70 to 160 ° C. and a pressure of 5 to 35 MPa React with the synthesis gas in the organic phase and the resulting 3 (4), 7 (8) -bisporylbicyclo [4,3,0] -nonane undergoes an oxidation reaction or first 3 (4), 7 The hydrogenation reaction is carried out with (8) -dihydroxymethylbicyclo [4.3.0] nonane and the diol thus obtained is reacted in an alkali melt.
priorityDate 2006-01-31^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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