http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0453189-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_46ffc67cd29dd51dbd0bc0e335dd3994
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D275-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06
filingDate 1991-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b88c0d492c950fa4f0159338e1dfeab3
publicationDate 1991-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0453189-A1
titleOfInvention Process for preparing isoxazolines
abstract Chiral oxazolines having the general formula:n wherein R is C₁ to C₁₀ alkyl or phenyl and the R¹ groups are independently hydrogen or C₁ to C₄ alkyl are prepared in substatially optically pure form by a process comprising the steps of (1) reacting a nitrile oxide of formula R-C=N-O with an acryloyl derivative of formula Z-COCH=C(R¹)₂ where Z is a moiety derived from a chiral sultam and n   (2) reacting the product of step (1) with a hydrogenating agent to produce the oxazoline and a chiral sultam of formula ZH. n The chiral oxalines described are useful as intermediates in e.g. the pharmaceutical or agrochemical industries.
priorityDate 1990-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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