http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103044313-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-88 |
| filingDate | 2012-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2014-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103044313-B |
| titleOfInvention | Method for synthesising carbazole compounds |
| abstract | The invention relates to a method for synthesising carbazole compounds, comprising the step of selectively reacting 1-(indol-2-yl)-3-alkyne-1-alcohol in the presence of gold trichloride in high region to synthesise functionalized carbazole. The method disclosed by the invention has the advantages that operation is simple, raw materials and reagents are available, conditions are moderate, the regioselectivity of the reaction is high, and the like; and moreover, a plurality of substituent groups can be introduced simultaneously, and the product is easily separated and purified. The method is suitable for synthesising various substituent carbazole compounds. |
| priorityDate | 2012-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.