http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20040017233-A

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D327-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D411-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D327-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 2002-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20040017233-A
titleOfInvention Stereoselective method for the preparation of nucleoside analogues
abstract The present invention relates to a method for producing an excellent cis nucleosides of the formula (A) or nucleoside homolog derivatives thereof,n n n n n n n n (Wherein R 1 is a pyridine base or a pharmaceutically acceptable derivative thereof and Q is oxygen, carbon, sulfur)n n n The process of coupling the pyridine base and the compound of formula (B) in an appropriate coupling solvent in the presence of a catalytic amount of an element or a combination of elements of group IB or IIB of the Periodic Table of Elements, in the presence of tertiary amines and Lewis acids ) To obtain an intermediate mixture, which is then deprotected to produce the compound of formula (A).
priorityDate 2001-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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