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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7bbf0cb262a0b75b400e780e8a078265
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-04
filingDate 2012-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0456e360219d9abcfd19f300e8487e9a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67e6894794e09fc293e0c75a1199bcd1
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publicationDate 2013-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2013056939-A
titleOfInvention Oligonucleotide synthesis
abstract The object of the present invention is to provide a method for preparing oligonucleotides that overcomes at least some of the disadvantages of the prior art. A method for preparing an oligonucleotide comprising: a) providing a hydroxyl group-containing compound having the formula (A); b) in the presence of an activator having the formula I (activator I). A step of preparing a phosphorylated compound by reacting the compound with a phosphorylating agent; c) in the presence of an activator II different from the activator I, the phosphorylated compound not isolated is represented by the formula (A): A method comprising reacting with a second compound. [Selection figure] None
priorityDate 2005-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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