http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1694691-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-167
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 2004-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f18a64414cd1a335201aaa32958bcf21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd815078df4514c9ae5ddddbea79d997
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8661d922e78b152ea2095b0eb33f16dc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28f9f13accf8ad6daf8744c56e8089dd
publicationDate 2006-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1694691-A1
titleOfInvention Improved synthesis of 2-substituted adenosines
abstract Synthesis of 2-substituted adenosines of formula (I) using 2-nitro pentabenzoyl adenosine, or 2-nitro pentaacetyl adenosine, as intermediate is described: Formula (I) wherein R = C1-6 alkoxy (straight or branched), a phenoxy group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-, cyano, nitro, C1-6 alkyl, or C1-6 alkoxy), a benzyloxy group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-, cyano, nitro, C1-6 alkyl, or C1-6 alkoxy), or a benzoyl group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-,cyano, nitro, C1-6 alkyl, or C1-6 alkoxy). The methods provide improved yield and purity of product.
priorityDate 2003-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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