http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-102014013462-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd24989c2801fbb18c11d531863f3ce6
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-08
filingDate 2014-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cad2cb3462f3bb706d502f2c6827dc0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1cf7f789e82bd20b1c71d2fb192aec1
publicationDate 2015-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-102014013462-A2
titleOfInvention ingenol-5,20-acetonide preparation method, preparation method of 3-ethynyl-3-hydroxy-4,7,7-trimethylbicyclo [4.1.0] heptane-2-carbaldehyde, preparation method of 2,2-dimethyl compound -4-ethynyl-5-triphenylphosphoranylidene-1,3-dioxane and intermediate
abstract ingenol-5,20-acetonide preparation method, preparation method of 3-ethynyl-3-hydroxy-4,7,7-trimethylbicyclo [4.1.0] heptane-2-carbaldehyde, preparation method of 2,2-dimethyl compound -4-Ethinyl-5-triphenylphosphoranylidene-1,3-dioxane and intermediate compound. The present invention relates to the method of preparing ingenol-5,20-acetonide as well as ingenol-5,20-acetonide obtained by such a process. The invention also relates to novel intermediate compounds in the preparation of ingenol-5,20-acetonide.
priorityDate 2014-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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