http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105152934-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-343
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
filingDate 2015-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_487a1c804e613a4a070d218e2741d81e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2776380152c97bae0af422439c8ca2a4
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publicationDate 2015-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105152934-A
titleOfInvention Catalytic asymmetric synthesis of axial chiral biaryl diphenols
abstract The invention discloses a method for catalyzing the asymmetric synthesis of axial chiral biaryl diphenols. In an organic solvent, using chiral phosphoric acid as a catalyst, the compound of formula I and the compound of formula II are reacted to obtain the compound of formula III: wherein, R 1 is an alkane Oxygen, ester, halogen, alkyl, hydroxyl, aryl, aldehyde or amide ; R2 is alkoxy, cyano, ester, alkyl, aryl, halogen or H. The present invention uses simple and easy-to-prepare raw materials under mild reaction conditions to synthesize axial chiral biaryl diphenols with high yield; the synthetic method of the present invention has good enantioselectivity, and the ee value of the obtained product Very high; the synthetic method of the present invention can tolerate multiple functional groups, and the substituent of 2-naphthol can be an electron-withdrawing substituent or an electron-donating substituent; the source of the catalyst used in the present invention is convenient, without heavy metal pollution, and has the prospect of realizing industrialization .
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107501160-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107501163-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105859527-A
priorityDate 2015-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 38.