http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0003578-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C405-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D301-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C405-00
filingDate 1998-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6ab2f332f3fea1f02818e468eaa45f6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ece036356b1bbfc5c059685bddf136bf
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publicationDate 2001-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0003578-A2
titleOfInvention A method for preparing epoxide intermediates for prostaglandins
abstract The present invention relates to a process for the preparation of novel epoxide intermediates of formula (I) for the preparation of 13,14-dihydro-prostaglandin derivatives A, E and F, wherein R is alkyl, carbocyclic aliphatic, heterocyclic aliphatic, aromatic or heteroaromatic; R 'is hydrogen, alkyl, carbocyclic aliphatic, heterocyclicaliphatic, aromatic or heteroaromatic, with the proviso that only one heteroatom is attached to 15-C; and Q is a suitable protecting group. New methyl (7-2-hydroxy-5- [2- (2-oxiranyl) ethyl] from commercially available methyl 7- (3- (R) -hydroxy-5-oxo-1-cyclopentylheptanoate) -4- (1,1,2,2-tetramethyl-1-silapropoxy) -cyclopentyl) -heptanoate can be readily coupled to O-, S- and N-containing nucleophiles in the presence of base or Lewis acid, and the products can be easily ring-opened compared to known lengthy processes 13,14-dihydroprostaglandin derivatives A, E and F can be prepared
priorityDate 1997-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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