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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C249-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-24
filingDate 1995-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7b739a612429c3986fc712304d2b035
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1de5b8582a72b903541b41c06c501dcf
publicationDate 1996-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08217735-A
titleOfInvention Optically active Schiff base and method for producing the same
abstract (57) [Summary] (Correction) [Structure] A salicylidene-type optically active Schiff base represented by the general formula [I]. (In the formula, X 1 represents an i-propyl group, a sec-butyl group or a t-butyl group, X 2 represents a hydrogen atom, a halogen atom, C1-10. Represents an alkoxy group or a C1-4 alkyl group. R 1 represents such also C1~6 alkyl group that is substituted with alkoxy or C1~4 alkylthio of C1-10, R 2 is alkoxy or C1~ of C1-10 4 represents a phenyl group which may be substituted with alkyl of 4. * Represents an asymmetric carbon. ) [Effect] Optically active α- It exhibits a particularly excellent effect as a ligand of an asymmetric complex catalyst when producing an acyloxyketone.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002241356-A
priorityDate 1995-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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