http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006096994-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2fc8c4f23758df7ed658973e2a913e38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ce509eafc06ba0dd740f8d7c81346839
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B37-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B35-02
filingDate 2006-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2acafda81d2337d0161b2413acd71c43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66aad76f7fcbe8db98936ec23b66e5aa
publicationDate 2006-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2006096994-A1
titleOfInvention Fluorous oxazolidinone chiral auxiliary compounds and methods of manufacture
abstract The present invention relates generally to perfluoroalkyl chiral auxiliary compounds and methods of manufacture. These compounds have the functionality to effectively support the synthesis of chiral compounds in single reactions, high-throughput parallel recations, or combinatorial reactions The invention relates to two oxazolidmone chiral auxiliaries (1) and (2): wherein Rf is a perfluoroalkyl group having the general formula (CH2)x-CyF2y+1 where x = 1-5 and y = 4-10 and wherein B is an unfunctionalized aryl, alkyl or arylalkyl group Pn a preferred embodiment, x = 2 and y = 6 and B is derived from unfunctionalized ammo acids The ammo acids may be from either the D- or L- series, and are preferably enantiomeπcally pure or in very high enantiomeric excess in either configuration.
priorityDate 2005-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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