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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-67
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-67
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-743
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-707
filingDate 1992-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba22a36b0ed961b59587894e8faa51c8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a48cb8be90afcd3b9f41ff9c47b2ea2
publicationDate 1993-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05238979-A
titleOfInvention Process for producing optically active 4-hydroxycyclopentenones
abstract (57) [Summary] [Structure] General formula [Chemical formula 1] (In the formula, R represents an alkyl group, an alkenyl group, or an alkynyl group. However, the substituent R at the 2-position and the hydroxyl group at the 3-position are in trans-coordination.) A general formula characterized by rearrangement of tenone alcohols while retaining a stereo structure. (In the formula, R has the same meaning as described above.) A method for producing an optically active 4-hydroxycyclopentenone. [Effect] Optically active 4-hydroxycyclopentenones can be obtained at low cost and industrially advantageously with high purity and high yield.
priorityDate 1992-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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