http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113402516-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_53b4d53983adbf56dd0e7d0bf96f8ce5 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 |
| filingDate | 2021-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4458c5827d404f6bd5bb708d18e9488b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a243638909a8b4ea0f388846ea7d7f8c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1736358dd44e47b9a1c392e13ade4e3d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_233fa1273bfea50f51cb2604d5477f9d |
| publicationDate | 2021-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-113402516-A |
| titleOfInvention | A method for the synthesis of isoquinolinone derivatives by the room temperature C-H activation/cyclization cascade reaction of N-chloroamides |
| abstract | The present invention provides a method for synthesizing isoquinolinone derivatives by a room temperature C-H activation/cyclization cascade reaction of N -chloroamides. Taking N -chloroamide as the guiding group and alkynedione as the coupling reagent, the C-H activation/cyclization cascade reaction at room temperature is realized under transition metal catalysis to synthesize isoquinolinone derivatives. Compared with other methods, the present invention has the following significant advantages: the C-H activation/cyclization cascade reaction at room temperature is mild, green and safe; the substrate is suitable for a wide range, and the terminal alkyne is tolerant. |
| priorityDate | 2021-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 99.