http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0727494-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-922
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-814
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-004
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
filingDate 1996-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1f7ed7364fede5f569136be7564f325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b413506e4297bae9c3f4d07df3666d8d
publicationDate 1996-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0727494-A1
titleOfInvention Method for the enzymatic acylation of alcohols with alkoxyvinylacetates through transesterification
abstract The invention relates to a process for the enzymatic acylation of primary and secondary alcohols with enol esters, in particular alkoxyvinyl acetates, in organic media, the enol ester being split into a simple ester formed after enolization and an acyl radical; this is transferred to the alcohol in the solution, the transfer taking place enantioselectively in the case of racemic or prochiral alcohols, i.e. H. selective acylation of only one enantiomer or pro-enantiomer takes place, leaving behind the free alcohol of the other enantiomer or pro-enantiomer. The chiral acylated compounds and unreacted chiral alcohols can easily be separated. The corresponding free alcohols can optionally be obtained from the acylated alcohols by simple ester cleavage.
priorityDate 1995-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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