http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104513116-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C269-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D321-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D321-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-205 |
| filingDate | 2014-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104513116-B |
| titleOfInvention | A kind of chiral amino formic acid esters and the synthetic method of derivant thereof |
| abstract | The present invention relates to a kind of chiral amino formic acid esters and the synthetic method of derivant thereof.Being reaction reagent with organic amine, nucleophilic addition is to having complete isostructural meso epoxyalkane and CO 2 Alternate copolymer and cause it to degrade, formed high antimer excess organic molecule chiral amino formic acid esters and derivant.This synthetic method has the Green Chemistry features such as mild condition, Atom economy and productivity are high, Merlon spatial configuration of its chiral carbon atom in organic amine nucleophilic addition degradation process is fully retained, produce enantiomeric excess value be up to 99% can functionalization hydroxy carbamate derivant.Carbamate and derivant thereof are important pesticide, medical important intermediate, and, SARS drug design complete synthesis at natural product is all with a wide range of applications. |
| priorityDate | 2014-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 85.