http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-9902743-A2
Outgoing Links
Predicate | Object |
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classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-675 |
filingDate | 1997-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b02b6e58c7859b0b3a48bf5310066086 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ce66f4b884bcb87dadd0fa402c4d075 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74931572fa8bb46d8e5cc92211bb747e |
publicationDate | 1999-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | HU-9902743-A2 |
titleOfInvention | Enzymatic process for the stereoselective production of therapeutic amides |
abstract | The present invention relates to a process for the preparation of a general formula (I) of an optically active compound in which E is a nitrogen mucilage or a CZ tuber, and in the incubator C is a ring member of carbon, when E is a tube roaster, an (A) X is an Ar-Y-tube distributor in which the Y-barrel is a spinner. in the case of a carbine, hydrofluoric, cyano, C 1 -C 4 alkyl and / or 1 to 4 carbonate alkyloxylcarboxylate, in the case of a hydrogen atom, a six-membered heterocyclic monocarboxylic acid alone or two nitrogens. a heterocaryl ring, or one or two nitrogen genes, and / or a five-membered heteroaryl ring containing a sulfur heterocyclic ring, and Z is hydrogen or a cyanogen, cyano, hydroxyl, C 1-4 alkyl or 1-4 carbon atomic radical; , and gives Z on the phenyl ring in which case, up to two halo, hydroglycyl, cyano, nitrogen, C 1-4 alkyl, and / or C 1-4 alkyloxy substituents are denaturing phenylthio, phenylsulfinyl or phenylfilyl; while the term "N" denotes a nitrogen atom, "X" may mean any of the apertures specified for X in the above (A), and the asterisk (*) represents an asymmetric center of gravity in a hypocritical manner, harboring a racemic compound of formula (II) wherein E and X are as defined above. And R1 represents one or more hydrofluorocarbon, halogen, C1-4alkyl, cyano, C1-4alkylamino and / or C1-4alkylalkylamino-lower alkylcarbonate, as appropriate, treated with a hydrazase enzyme. The invention further extends to the synthesis of useful intermediary intermediates for the synthesis of the above-mentioned compounds and the preparation thereof. ŕ |
priorityDate | 1997-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 169.