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filingDate 2011-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90d794e19f5b92ed013d55e22df201b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_667300d30cd11fd48c2f1e9ccb852fbd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77611cf3c740507af6af0b3b3028f815
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ef7dbbf3e35e476faf973d1e7632273
publicationDate 2018-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2794671-C
titleOfInvention Stereoselective synthesis of phosphorus containing actives
abstract Disclosed herein are phosphorus-containing actives, their use as actives for treating diseases, and a stereoselective process for preparing the same. Also disclosed herein are useful synthetic intermediates and processes for preparing the same. A process for preparing a composition comprising an enantiomerically- or a diastereomerically-enriched phosphorus-containing active, salt, or pharmaceutically acceptable salt thereof, of formula I is disclosed: 1 which comprises a) reacting a protected or unprotected Active with a base to form a salt of said active and then reacting said salt with an enantiomerically- or a diastereomerically enriched compound of formula II wherein Group is as defined herein, W is an aryl or -CCH2)nSC(O)C(CH3)m(CH2OH)3-m, where n is 2 or 3 and m is 0, 1, 2, or 3, and LG is a leaving group; b) optionally deprotecting the compound obtained in step a) and c) optionally subjecting the compound obtained in step a) or the compound obtained in step b) to chromatography, extraction, or crystallization to obtain the active.
priorityDate 2010-03-31-04:00^^<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: 1163.