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filingDate 2003-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9179c9ee19b6aab7926b0c0810c0cb8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25240ccb300a3fde6b3adaf9866cb31e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee682bf3ea469452b0968ef7c5239953
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8db85b86177a4c4e41ffbceac4cc13f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39b0e45ea6422ceee96da46378b5240d
publicationDate 2004-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004138468-A1
titleOfInvention Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
abstract One aspect of the present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-sulfur bond between the sulfur atom of a thiol moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper(II)-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-carbon bond between the carbon atom of cyanide ion and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In another embodiment, the present invention relates to a copper-catalyzed method of transforming an aryl, heteroaryl, or vinyl chloride or bromide into the corresponding aryl, heteroaryl, or vinyl iodide. Yet another embodient of the present invention relates to a tandem method, which may be practiced in a single reaction vessel, wherein the first step of the method involves the copper-catalyzed formation of an aryl, heteroaryl, or vinyl iodide from the corresponding aryl, heteroaryl, or vinyl chloride or bromide; and the second step of the method involves the copper-catalyzed formation of an aryl, heteroaryl, or vinyl nitrile, amide or sulfide from the aryl, heteroaryl, or vinyl iodide formed in the first step.
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priorityDate 2002-08-02-04:00^^<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/substance/SID455431039
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68976
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142692508
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223737534
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71250739
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399377
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12408998
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21226206
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226450233
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142692511
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID249030314

Total number of triples: 1242.