http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2657797-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
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filingDate 2007-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8482cc0cacf5e3dd571e5d47c7887389
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cd0bab508b74138480ffba3209579c2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_848f771deef2afc6710f13db7a9aadb2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_921a84e169fb7c5c0546ca26ede45876
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf31cf997990e5ef548a8472410ee329
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55a2897c477d24318bec2d821fcf4317
publicationDate 2008-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2657797-A1
titleOfInvention Tetrahydrofuro [3, 2-b] pyrrol-3-one intermediates
abstract The present invention relates to a process for preparing a compound of formula (Ia), (Ib), (Ic) or (Id), or a pharmaceutically acceptable salt, hydrate, solvate, complex or prodrug thereof, said process comprising the steps of: (A) (i) treating a compound of formula (IVa), where R48 is alkyl or tosyl, with an oxidising agent to form a compound of formula (Va); and (ii) converting said compound of formula (Va) to a compound of formula (Ia) or (Ic); or (B) (i) treating a compound of formula (IVb), where R48 is alkyl or tosyl, with an oxidising agent to form a compound of formula (Vb); and (ii) converting said compound of formula (Vb) to a compound of formula (Ib) or (Id).
priorityDate 2006-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 561.