http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5079359-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6bfdf49224a405be1f7b653c56ebad94
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F17-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F17-02
filingDate 1990-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_109c4ec108bbc15d96094410e778bd35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16887ef411efade7b7e81a2c21f1f1f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f116624ee83d476d7a4c95757c31c59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dcdcb59fcc5a77c437248d674c35ca06
publicationDate 1992-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5079359-A
titleOfInvention Chiral amino-methyl ferrocene derivatives
abstract A ferrocene derivatives represented by the following formula (I): <IMAGE> (I) can be a useful ligand to metals with Lewis acidity and is used as a catalyst for asymmetric synthesis with good enantioselectivety. This ferrocene derivatives is synthesized from a novel haloferrocene derivative represented by formula (II) and the haloferrocene derivative is synthesized from a novel ferrocene derivative represented by formula (III).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006095181-A2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006095181-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103772442-A
priorityDate 1989-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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