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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_107ea2b8f946a3d2e1a7edf0e96121db
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G61-02
filingDate 1997-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a731c47c3c8abecc9029db4738bf1385
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7473be4b1fc8ea2f74bf64224db41949
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b505f40b4615ab42ab3f1d44bd326d6c
publicationDate 2000-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6020452-A
titleOfInvention Chiral biphenyl compounds for use in asymmetric reactions
abstract A chiral biphenyl compound includes a hindered 2,2'-substituted-1,1'-biphenyl subunit and has the following formula: The chiral biphenyl compounds have been shown to be useful as catalysts in asymmetric reactions. For example, an organozinc species can be formed by reacting the chiral biphenyl compound with an organozinc compound, R14R15Zn and then used as a catalyst for the asymmetric alkylation of an aldehyde by an organozinc compound.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018089165-A1
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priorityDate 1996-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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