http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2419768-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/C07C307-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-36 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C307-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-36 |
filingDate | 2001-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b66254af634a66aed862ae722e9a4870 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7f86481229402af3494fedcf196c614 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f7be269e609599ae18bb0d1882b781a |
publicationDate | 2002-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-2419768-A1 |
titleOfInvention | Amino acid-derived, 7-membered cyclic sulfamides and methods of synthesizing the same |
abstract | New sulfamide compounds and methods of forming those compounds are provided. The inventive methods comprise subjecting a template opened-ring sulfamide compound to a ring-closing metathesis reaction in the presence of a Grubbs catalyst to yield a heterocyclic sulfamide. Advantageously, the template structures can be provided with a wide array of functional groups (e.g., substituted and unsubstituted amino acid side chains, peptides) chosen to provide particular properties to the compound. The preferred heterocyclic sulfamides are represented by a formula selected from the group consisting of formulae (I), (II), (III), and (IV). |
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: 36.