http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H1180097-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-14
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filingDate 1997-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5811247b3ac79f62fdb8f5ab7fc7a55e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_570e44084f811274b28e6dbf7bc03576
publicationDate 1999-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1180097-A
titleOfInvention Method for producing optically active bicyclo derivative and novel bicyclo derivative
abstract (57) Abstract: Provided is an optically active bicyclo derivative which can be an important synthetic intermediate of many natural products and / or bioactive compounds by a catalytic asymmetric intermolecular-intramolecular tandem nitroaldol reaction. . An aldehyde of the formula (1) is obtained by an asymmetric intermolecular-intramolecular tandem nitroaldol reaction using an asymmetric synthesis catalyst using a metal complex obtained by reacting an optically active binaphthol or a binaphthol derivative with a rare earth compound. From the compound and nitromethane, an optically active bicyclo derivative of formula (3), which is important for supplying raw materials for medicines, pesticides, fragrances, and liquid crystal intermediates, can be produced in a single step. Embedded image [In the formulas (1) and (3), R 1 represents an alkyl group having 1 to 3 carbon atoms, Y represents O, S or H 2 , m represents an integer of 2 to 4, and n represents 2 to 2. Represents an integer of 5. ]
priorityDate 1997-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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