http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016074646-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b1276d47865180ac49879b05af77d3ae |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C327-42 |
| filingDate | 2014-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee2107ed9ebed48b624340490bef18c8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_19f6985b9bdc35d6b0b98a42bc895c43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a94f504818e672b2e164d0dbaff797f6 |
| publicationDate | 2016-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2016074646-A |
| titleOfInvention | Thiamide derivative |
| abstract | The present invention provides a thioamide derivative that is used for a novel bioorthogonal novel click reaction that does not require an additive and proceeds even in an aqueous solution under mild conditions. For example, the following thioamide derivatives. (R1 is an alkyl group; R2 is 1) a C1-C6 alkylene having an amino group or a site where the amino group is carbamate-protected, and 2) the amino group or the amino group is carbamate-protected. A C1-3 alkylene bonded to a C1-3 alkylene terminated by a 1-6 methyleneoxymethylene chain, or 3) a C1 having a carboxyl group or an activated group thereof 6 alkylene. ) [Selection figure] None |
| priorityDate | 2014-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 48.