http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2354476-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C279-36
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filingDate 1999-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7861e8f825f3acec45a8721568653ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36c2251be3d7032bf729be043a5f6cc5
publicationDate 2000-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2354476-A1
titleOfInvention Methods for the synthesis of alpha-hydroxy-beta-amino acid and amide derivatives
abstract Methods for the synthesis of .alpha.-hydroxy-.beta.-amino acid and amide derivatives and .alpha.-ketoamide derivatives and novel derivatives made by these methods are provided. These methods involve reacting an N-terminally blocked (protected) aminoaldehyde with an isonitrile and a carboxylic acid to give an amino-.alpha.-acyloxy carboxamide. The acyloxy group may be removed to give the derivative. Alternatively the protecting group is removed and acyl shift occurs to give the derivative. These derivatives are useful in the synthesis of compounds such as peptidyl .alpha.-ketoamides and .alpha.-hydroxy-.beta.-carboxylic acid and amide derivatives. Certain of these compounds have been reported to have activity as inhibitors of proteases, such as serine proteases and cysteine proteases.
priorityDate 1998-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 905.