http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2076133-A2

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filingDate 2007-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e37f4042a87dcf65c296e0c06de3783a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c8c0e376548f396e65ab6399ca39310
publicationDate 2009-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2076133-A2
titleOfInvention Synthesis of enone intermediate
abstract The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The recent development of a modular synthesis of tetracycline analogs through a chiral enone intermediate has allowed for the efficient synthesis of novel tetracycline analogs never prepared before. The present invention provides a more efficient route for preparing the enone intermediate.
priorityDate 2006-10-11-04:00^^<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: 1040.