http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8088346-B2

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5bc5292a07e34d16eb1d033a16d3aec3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f2991172bd6a577d793fe35e544bab3a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B37-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01G55-00
filingDate 2008-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9c839554cbb5a9319a45c72bb7b1f4a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42e46c03ad5b7b1a421171acdc701e3b
publicationDate 2012-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8088346-B2
titleOfInvention Alkene hydrofunctionalization reactions
abstract A reductive cross coupling reaction process for functionalization of a nucleophilic alkene can be achieved. The nucleophilic alkene and a nucleophilic cross coupling partner compound can be reacted in the presence of an oxidizable alcohol and a suitable catalyst to form a reductive coupling product. Various additives can also be useful to refine the process such as by mitigating certain undesirable intermediates, facilitating specific site selectivity for various substitutions or reaction sites, etc. Chiral additives can be optionally used which act to provide asymmetric catalysis, e.g. allow for regioselective and stereoselective production of reductive coupling products. A reductive cross coupling pathway can include oxidizing the oxidizable alcohol to form a catalyst hydride. The nucleophilic alkene can be inserted into the catalyst hydride to form a catalyst-alkyl intermediate. Further, the catalyst-alkyl intermediate can be transmetallized with the nucleophilic cross coupling partner compound to form a transmetallated intermediate. The catalyst can be reductively eliminated to form the reductive coupling product and a reduced catalyst. Finally, the reduced catalyst can be oxidized under aerobic conditions, for example with oxygen, to form the oxidized catalyst and subsequent repetition through the cyclic pathway.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021118931-A1
priorityDate 2007-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57615057
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245160554
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57615059
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7501
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127367713
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11136797
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57615062
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410492059
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448020525
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12160751
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449649348
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57615072
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424651693
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411460564
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415942271
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127815183
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546721
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228769639
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57615073
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406941890
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID332297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228768922
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226400488
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160669737
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228768923
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243224902

Total number of triples: 327.