http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107011278-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a767f4998e53684ec68f4fdfbb8e4de7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
filingDate 2017-04-06^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1a33c63e848aa5e1abbc1fc1c4303d2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5de206b0df468c5d735f677e6d52139a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34b98c47044001e74c418d3c5b25818a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_022d7b408a5a5646c1de1b7f6c4e9a47
publicationDate 2017-08-04^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107011278-A
titleOfInvention 3,4,5‑, Trisubstituted‑4,5‑dihydroisoxazole, derivatives and their synthesis method and use
abstract A 3,4,5-trisubstituted-4,5-dihydroisoxazole and its derivatives as well as their synthesis method and application. The present invention mainly relates to a method for synthesizing isoxazoline compounds. No catalyst is needed for the synthesis. Aldehydes and oxime esters are converted into isoxazolines and their compounds only under the action of alkali and organic solvents are used as solvents. The technical scheme of derivatives; it overcomes the complex synthetic steps in the existing synthetic methods of isoxazoline compounds, which requires multi-step synthetic processes to complete, and also requires the use of metal catalysts, chemically equivalent metal oxidants or peroxides Difficulty; it maintains atom economy to the greatest extent; it has stable molecular structure, excellent chemical properties, molecular dicing and compound fragments contain rich biological and pharmacological activities; it also has simple reaction system, mild reaction conditions, Fewer reaction equipment, simple experimental operation, wide sources of materials, high yield, easy expansion of users and applications, high product utilization value, predictable market commercialization prospects, etc.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110551098-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108191785-A
priorityDate 2017-04-06^^<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-105622537-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101522672-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105198888-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466349001

Showing number of triples: 1 to 34 of 34.