http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0214331-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_94b51d317764e2f4f1bbcb355b274c8b |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65844 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4465 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4484 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6584 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-44 |
filingDate | 2001-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10d191ac4c78c2711a9eb33d61544c37 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b66254af634a66aed862ae722e9a4870 |
publicationDate | 2002-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | WO-0214331-A1 |
titleOfInvention | Amino acid-derived phosphonamidic anhydrides and methods of preparing the same |
abstract | New phosphonamide compounds and methods of forming those compounds are provided. The inventive methods comprise forming a template opened-ring phosphonamide compound and optionally subjecting the template to a ring-closing metathesis reaction in the presence of a ring-closing catalyst (e.g., a Grubbs catalyst) to yield a heterocyclic phosphonamide. Advantageously, the template structures can be provided with a wide array of functional groups (e.g., amino acid side chains, peptides) chosen to provide particular properties to the compound. The preferred heterocyclic phosphonamides are represented by formula (I). |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013023454-A |
priorityDate | 2000-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 132.