http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5585252-A

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filingDate 1994-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1996-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0bd3397aed91db04647847e416a39de
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_366fdfcce093d6144b58917b255700c8
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publicationDate 1996-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5585252-A
titleOfInvention Enantio- and regioselective synthesis of organic compounds using enol esters as irreversible transacylation reagents
abstract A process for irreversible regio- and stereoselective enzyme catalyzed acylation of alcohols using enol esters as acylating reagents is disclosed. The present invention permits the selective modification of hydroxyl group(s) of chiral and meso alcohols, including sugars, organometallics, and glycosides. The enol freed upon transesterification rapidly tautomerizes to the corresponding volatile aldehyde or ketone thereby preventing the reverse reaction from occurring.
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priorityDate 1988-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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