http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7763734-B2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-52
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filingDate 2007-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a344439c3be7771d6692dfc5d39fa31
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_922e0c176a2425debdd4a6eda83a0d8b
publicationDate 2010-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7763734-B2
titleOfInvention Synthesis, structure and use of bisoxazolidines for asymmetric catalysis and synthesis
abstract One aspect of the invention relates to chiral bisoxazolidines and their use in asymmetric catalysis. The chiral bisoxazolidines are a novel class of compounds that is expected to find multiple applications, for example, in asymmetric synthesis. For example, a bisoxazolidine ligand enabled the catalytic enantioselective alkynylation and alkylation of a range of aromatic and aliphatic aldehydes, generating chiral propargylic alcohols and secondary alcohols in high yields and enantiomeric excess.
priorityDate 2006-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1659.