http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007119402-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8d35e17017d13a5b026b605aefc3d34c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-293
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-343
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-343
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-773
filingDate 2007-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61672eb71171961d8cfac89e859d7c33
publicationDate 2007-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007119402-A1
titleOfInvention Method for producing 1,2-phenylethane compound using atom transfer radical coupling reaction
abstract Disclosed is a method for producing an 1,2-phenylethane compound with an extremely high yield through a short-time reaction. Specifically disclosed is a method for producing an 1,2-phenylethane compound, wherein a compound represented by the formula (II) below is produced by subjecting a compound represented by the formula (I) below to a coupling reaction in the presence of a transition metal complex. [Chemical formula 1] (I) (In the formula, Ra represents a hydrogen atom or a substituted or unsubstituted phenyl group; Rb represents a hydrogen atom or a substituent, n represents an integer of 1-5, and when n is not less than 2, Rb's may be the same as or different from each other and may combine together to form a ring; and X represents a halogen atom.) [Chemical formula 2] (II)
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110015960-A
priorityDate 2006-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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