http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013253104-A

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filingDate 2013-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c48cdcce22855dbeb5ef17b067d85c6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7a22985a719555bcb8b79d0d9202086
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93e3a784c6869b2c701e29fc6983ca56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f90fe444661afb0ed5c34efa2fcd210c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc0328f0e4323c6862f53dc1a527371f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cd68ec74772bf6a8e425632c103163a
publicationDate 2013-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2013253104-A
titleOfInvention De novo synthesis of complex
abstract A novel method for the production of PEG conjugates of pharmaceutically active compounds is provided. In one or more embodiments of the invention, a method of synthesizing a complex of pharmaceutically active compounds is provided, the method comprising one or more synthetically available intermediate compounds. Attaching at least one water-soluble oligomer directly or via a linker group at a position and completing the synthetic route to yield a complex of pharmaceutically active compounds. The method of the present invention advantageously provides, inter alia, “denovo” synthesis, wherein the intermediate is covalently linked to the water soluble oligomer and the remainder of the complex is then synthesized from the water soluble oligomer intermediate. [Selection figure] None
priorityDate 2007-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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