http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4045518-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-657181
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6571
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-5357
filingDate 1975-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1977-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22f0fcf6704a3e8fa95af8f03328ef1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edb2e12d7e59b16770e431430052a0f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a210cb889a84ed7b8e13f0c73df51a2
publicationDate 1977-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4045518-A
titleOfInvention 1,2-Oxaphospholanes
abstract 2-Oxo-2-alkoxy-5-dialkylphosphono-1,2-oxaphospholanes of the formula <IMAGE> in which R1 to R7 are hydrocarbon radicals can be prepared from alpha , beta -unsaturated ketones and 2 or more moles of a dialkyl phosphite. Obviously alpha -ketophosphonates are intermediates of this reaction, as these compounds react with 1 or more moles of dialkyl phosphite in yielding the oxaphospholanes too. Both reactions are promoted by alkaline catalysts.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006207457-A1
priorityDate 1973-09-07-04:00^^<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: 613.