http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105130722-B

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-215
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B37-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C15-54
filingDate 2015-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105130722-B
titleOfInvention The monosubstituted 1,3,5 s-triazine compound of 1,2,3 triazoles cooperates with CuSO4·5H2The method of O catalytic decarboxylation coupling reactions
abstract The invention discloses a kind of monosubstituted 1,3,5 s-triazine compound of 1,2,3 triazole cooperates with CuSO 4 ·5H 2 The method of O catalytic decarboxylation coupling reactions, the method is with good stability, CuSO cheap and easy to get 4 ·5H 2 O and be catalyst system and catalyzing to water, air-stable, the high compound in triazine class to sense dough, the decarboxylation coupling reaction of catalysis halogenated aryl hydrocarbon and phenylpropiolic acid, the reaction system is without using traditional Phosphine ligands, reduce environmental pollution, and with good substrate applicability, the easily separated purification of target product high income.The present invention is a kind of decarboxylation coupling reaction system efficiently, safe, can be applicable to a step and constructs Csp Csp 2 Key.
priorityDate 2015-08-24-04:00^^<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: 49.