http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1055078-A

Outgoing Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J3-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00
filingDate 1964-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1055078-A
titleOfInvention 17 beta methyl-20-alkyl-18-nor-17 alpha -pregnenes
abstract Novel steroids of the formula <FORM:1055078/C2/1> wherein the A and B rings have one of the structures <FORM:1055078/C2/2> (wherein R is C1-4 alkyl and R1 and R11 ar each either hydrogen or acetyl) are prepared by reacting steroids of the formula <FORM:1055078/C2/3> (wherein the A and B rings have one of the 3-hydroxy or -acyloxy-containing structures depicted above) with an alkyl Grignard reagent at a temperature between - 10 DEG and + 30 DEG C. in an inert, anhydrous, organic solvent with subsequent mild hydrolysis in water, to give a steroid of the first general formula above wherein R11 is hydrogen and the A and B rings are as in the starting material. Then subsequently 3b -acetates are hydrolysed to 3b -ols, the 3b ,16a -diols are acetylated to the diacetates (which can also be obtained by acetylation of the 3-mono-acetates) and these may be hydrolysed to give the 3b ,16a -diols again. The D 5-3-ols or their acylates may be catalytically hydrogenated to the 5,6-saturated compounds. The D 4-3-ones are prepared by oxidation of the D 5-3-ols, and on catalytic hydrogenation they yield the ring A saturated 3-ones. The 16-monoacetoxy compounds are prepared by standard methods from the 3-oxo-16-ols.
priorityDate 1963-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 28.