http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0010986-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-36
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-36
filingDate 1999-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12add1c6d1539b64898ca85e75dfec5b
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publicationDate 2000-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0010986-A1
titleOfInvention Process for the preparation of (2r, 3s)-3-amino-1,2-oxirane
abstract A process for the preparation of (2R, 3S)-3-amino-4-phenylbutane-1,2-epoxide, which comprises treating a (2S, 3S)-3-amino-1-halo-2-hydroxy-4-phenylbutane or (2S, 3S)-3-amino-4-phenylbutane-1,2-epoxide either with a quaternary ammonium carboxylate or with both a metal carboxylate and a quaternary ammonium salt to prepare a (2S, 3S)-1-acyloxy-3-amino-2-hydroxy-4-phenylbutane, treating this compound with a sulfonyl halide in the presence of an organic base to prepare a (2S, 3S)-1-acyloxy-3-amino-2-sulfonyloxy-4-phenylbutane, and subjecting the compound thus obtained to treatment with an inorganic base. This process makes it possible to efficiently produce intermediates for HIV protease inhibitors by using L-phenylalanine as a raw material.
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Total number of triples: 27.