http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11116542-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c95bc8f44f78158b5245b623a6c0109e |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-14 |
| filingDate | 1997-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad24723ab38a6375ae0321c7d8c74fa8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f80d8b5b58aa52469680f7b9f13cf64 |
| publicationDate | 1999-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H11116542-A |
| titleOfInvention | Process for producing gamma-glutamic amides |
| abstract | (57) Abstract: γ-glutamic acid amide such as theanine is synthesized according to the following reaction formula 1. Embedded image In particular, the use of the N-substituted pyrrolidonecarboxylic acid represented by the formula 1 enables theanine and the like to be obtained in a high yield in a reaction at room temperature and normal pressure for only a few hours without using 100% amine. And is particularly excellent as an industrial synthesis method. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100450996-C |
| priorityDate | 1997-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 57.