http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101109845-B1

Outgoing Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C68-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-013
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-54
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-385
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-587
filingDate 2004-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101109845-B1
titleOfInvention Method for producing cyclocyclic ketones and intermediates thereof
abstract Provided is a method for producing a mousse cone by the 1,4-conjugated methyl addition reaction of 2-cyclopentadecenone in a high yield under practical conditions without being subjected to cryogenic or low concentration reaction conditions. do.n n n In the method of the present invention, 1,4-conjugated addition reaction is carried out to 2-cyclopentadecenone with a methylated organometallic reagent in the presence of a copper catalyst or a nickel catalyst and an enol anion scavenger, and is represented by the general formula (II). ):n n n n n n n n The 3-methyl-1-cyclopentadecene derivative shown by this is obtained, Next, a muscon is obtained by solvolysis of the enol part of this 3-methyl-1-cyclopentadecene derivative.
priorityDate 2004-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424847942
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10877069

Total number of triples: 27.