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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af99df08b153738cd418446a75d09bfc
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-18
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0217
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-20
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-20
filingDate 1996-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42dc646ee88690410e4e670369649e8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123547b186500a05120c0f8245ae28e6
publicationDate 1997-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2230272-A1
titleOfInvention Isomerization of bisphenols
abstract A catalyst useful for the condensation of an aldehyde or ketone starting material with a phenol was an insoluble mercaptosulfonic acid compound. The heterogeneous catalysts comprise catalytically-active species represented by formula (II). L was an optional linking group and - was a bond, which catalytically-active species was attached by the bond - to an insoluble organic or inorganic support; or a catalytically-active species represented by formula (III), wherein L' was an optional linking group, - was a bond and .theta.' and .theta." were residues of .theta., and a and b were independently selected from integers equal to or greater than 1. These catalysts isomerize o,p-bisphenols to p,p-bisphenols.
priorityDate 1995-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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