http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8350022-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_61894a6a8c2f1b045ada03b2506db369
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ee559ff883e40f9910be262c447333e8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_96a9420efe237f58621775a2dceab1a7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-00
filingDate 2009-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34c3983a603a49aa24f57611b7e3472b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_117c0bbc8c09596d7caa1d1277a92847
publicationDate 2013-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8350022-B2
titleOfInvention Method for the stereoselective synthesis of phosphorus compounds
abstract The present invention relates to a method for stereoselective synthesis of phosphorus compounds, whereby in the first reaction step a chiral auxiliary on the phosphorus atom of phosphoryl chloride, thiophosphoryl chloride or phosphorus trichloride is covalently bonded, the product from the first reaction step is reacted in the following step with an alcohol, thiol, or amine as the nucleophile in the presence of a base, and in the last step the chiral auxiliary is displaced from the product of the following step by a nucleophile.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10280192-B2
priorityDate 2008-04-04-04:00^^<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: 425.