http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106242935-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d40285e27f4ed83b8728b0d477404958
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C41-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-42
filingDate 2016-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fac74cbc0e6c2ccca73ca42896090009
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_578a9fc32187751904b60360f52d5adb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46eaf556003d3d31301d35c624ee27b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bda75673f32c7d2ec73b131f0978afd5
publicationDate 2016-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106242935-A
titleOfInvention A kind of synthetic method of triaryl substituted chiral compound
abstract The present invention provides a kind of synthetic method of the triaryl substituted chiral compound shown in formula (1), described synthetic method is: in water-oil two-phase system, the 2-(aryl group shown in raw material formula (2) (p-toluenesulfonyl) methyl) phenol and the 2-naphthol shown in formula (3) react under the effect of acid-binding agent, chiral catalyst, TLC tracking monitors to reaction completely, afterward reaction solution is through aftertreatment, Obtain the triaryl substituted chiral compound shown in product formula (1); The present invention uses the chiral catalyst containing at least one tertiary amine and nitrogen squarylium functional group as the catalytic system, reacts in water-oil two-phase, post-treatment The isolated product triaryl-substituted chiral compound can be used as a class of important organic intermediates in the fields of medicine, pesticides and the like; the method of the invention has the advantages of low solvent pollution, fast reaction speed, high yield, good asymmetric selectivity, and low reaction bottom. It has a wide range of substances, and the reaction reagents are cheap and easy to obtain, which has important application value;
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113004109-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110950793-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110950793-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109896999-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109896999-A
priorityDate 2016-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102557955-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153261641
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415216715
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425935677
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID149598480

Total number of triples: 35.