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filingDate 2005-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-04-03-04:00^^<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_2847a9a5e121846140182921c4464648
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51cb0fcb85ac08d68f58fd1e017c45ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df31f673dafb6f62f303bd51147d41c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10536db575b1f17dcfce2aa4b2277dd9
publicationDate 2012-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2566464-C
titleOfInvention Synthesis of tetracyclines and analogues thereof
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 modular synthesis of tetracyclines and tetracycline analogs described provides an efficient and enantioselective route to a variety of tetracycline analogs and polycyclines previously inaccessible via earlier tetracycline syntheses and semi-synthetic methods. These analogs may be used as anti-microbial agents or anti-proliferative agents in the treatment of diseases of humans or other animals. The present invention relates to an enone represented by a compound of the formula: (see above formula) wherein R3, R4, R5, R6 and P' are as defined herein.
priorityDate 2004-05-21-04:00^^<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: 693.