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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-26
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
filingDate 2014-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104353491-B
titleOfInvention For the synthesis of a catalyst for chiral secondary alcohol, the chiral secondary alcohol synthetic method of its preparation method and this catalyst of employing
abstract The present invention relates to catalytic chemistry field, be specifically related to a kind of catalyst for the synthesis of chiral secondary alcohol, the chiral secondary alcohol synthetic method of its preparation method and this catalyst of employing. This catalyst is the complex compound that diethyl zinc and chiral ligand reaction generate, and described chiral ligand is that employing furans dialdehyde, potassium hydroxide and amino acid are the schiff bases that raw material chemical reaction generates. This catalyst has the advantages such as natural abundance is large, reaction condition is gentle, energy consumption is low, equipment requirement is low.
priorityDate 2014-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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