Fremgangsmåde til fremstilling af (S)-cyanhydriner
Preparation of (S)-cyanohydrin compounds of formula (I) comprises enzyme-catalysed reaction of carbonyl compounds of formula (II) with hydrocyanic acid, or a substance which releases hydrocyanic acid or CN, in the presence of a catalytic amount of an (S)-oxynitrilase immobilised on a nitrocellulose...
Gespeichert in:
Hauptverfasser: | , , , |
---|---|
Format: | Patent |
Sprache: | dan |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | EFFENBERGER, FRANZ, DR ROOS, JUERGEN WAJANT, HARALD FOERSTER, SIEGFRIED |
description | Preparation of (S)-cyanohydrin compounds of formula (I) comprises enzyme-catalysed reaction of carbonyl compounds of formula (II) with hydrocyanic acid, or a substance which releases hydrocyanic acid or CN, in the presence of a catalytic amount of an (S)-oxynitrilase immobilised on a nitrocellulose carrier. R, R' = H; 1-18C alkyl, 2-18C alkenyl or 2-18C alkynyl (all optionally substituted by ≥ 1 amine, imine, OH, 1-6C alkoxy, halo, carboxyl, 3-20C cycloalkyl and/or Het substituents, where the cyclic substituents are themselves optionally substituted by ≥ 1 halo, OH, 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl); or a (hetero)aromatic group containing 5-22 ring atoms, in which up to 4 ring C atoms may be replaced by N, O and/or S atoms, the ring being optionally substituted by ≥ 1 amine, imine, OH, 1-8C alkoxy, aryloxy, halo, carboxy or 1-22C optionally unsaturated alkyl, where ≥ 2 of the ring substituents may combine to form a cyclic group; Het = an aromatic ring with up to 22C atoms which is optionally substituted by N, O or S heteroatoms; provided that R' and R are not both H. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DK0799894TT3</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DK0799894TT3</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DK0799894TT33</originalsourceid><addsrcrecordid>eNrjZDB2K0rNTU_MSy_OPbw0JVWhJDNHIQ0oVAxk5GTmpSskpiloBGvqJlcm5mVUphRl5qUW8TCwpiXmFKfyQmluBkU31xBnD93Ugvz41OKCxOTUvNSSeBdvA3NLSwtLk5AQY2Ni1AAARqItXw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Fremgangsmåde til fremstilling af (S)-cyanhydriner</title><source>esp@cenet</source><creator>EFFENBERGER, FRANZ, DR ; ROOS, JUERGEN ; WAJANT, HARALD ; FOERSTER, SIEGFRIED</creator><creatorcontrib>EFFENBERGER, FRANZ, DR ; ROOS, JUERGEN ; WAJANT, HARALD ; FOERSTER, SIEGFRIED</creatorcontrib><description>Preparation of (S)-cyanohydrin compounds of formula (I) comprises enzyme-catalysed reaction of carbonyl compounds of formula (II) with hydrocyanic acid, or a substance which releases hydrocyanic acid or CN, in the presence of a catalytic amount of an (S)-oxynitrilase immobilised on a nitrocellulose carrier. R, R' = H; 1-18C alkyl, 2-18C alkenyl or 2-18C alkynyl (all optionally substituted by ≥ 1 amine, imine, OH, 1-6C alkoxy, halo, carboxyl, 3-20C cycloalkyl and/or Het substituents, where the cyclic substituents are themselves optionally substituted by ≥ 1 halo, OH, 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl); or a (hetero)aromatic group containing 5-22 ring atoms, in which up to 4 ring C atoms may be replaced by N, O and/or S atoms, the ring being optionally substituted by ≥ 1 amine, imine, OH, 1-8C alkoxy, aryloxy, halo, carboxy or 1-22C optionally unsaturated alkyl, where ≥ 2 of the ring substituents may combine to form a cyclic group; Het = an aromatic ring with up to 22C atoms which is optionally substituted by N, O or S heteroatoms; provided that R' and R are not both H.</description><edition>7</edition><language>dan</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; ENZYMOLOGY ; FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; ORGANIC CHEMISTRY ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2004</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20040809&DB=EPODOC&CC=DK&NR=0799894T3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20040809&DB=EPODOC&CC=DK&NR=0799894T3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>EFFENBERGER, FRANZ, DR</creatorcontrib><creatorcontrib>ROOS, JUERGEN</creatorcontrib><creatorcontrib>WAJANT, HARALD</creatorcontrib><creatorcontrib>FOERSTER, SIEGFRIED</creatorcontrib><title>Fremgangsmåde til fremstilling af (S)-cyanhydriner</title><description>Preparation of (S)-cyanohydrin compounds of formula (I) comprises enzyme-catalysed reaction of carbonyl compounds of formula (II) with hydrocyanic acid, or a substance which releases hydrocyanic acid or CN, in the presence of a catalytic amount of an (S)-oxynitrilase immobilised on a nitrocellulose carrier. R, R' = H; 1-18C alkyl, 2-18C alkenyl or 2-18C alkynyl (all optionally substituted by ≥ 1 amine, imine, OH, 1-6C alkoxy, halo, carboxyl, 3-20C cycloalkyl and/or Het substituents, where the cyclic substituents are themselves optionally substituted by ≥ 1 halo, OH, 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl); or a (hetero)aromatic group containing 5-22 ring atoms, in which up to 4 ring C atoms may be replaced by N, O and/or S atoms, the ring being optionally substituted by ≥ 1 amine, imine, OH, 1-8C alkoxy, aryloxy, halo, carboxy or 1-22C optionally unsaturated alkyl, where ≥ 2 of the ring substituents may combine to form a cyclic group; Het = an aromatic ring with up to 22C atoms which is optionally substituted by N, O or S heteroatoms; provided that R' and R are not both H.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS THEREOF</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>ORGANIC CHEMISTRY</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2004</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDB2K0rNTU_MSy_OPbw0JVWhJDNHIQ0oVAxk5GTmpSskpiloBGvqJlcm5mVUphRl5qUW8TCwpiXmFKfyQmluBkU31xBnD93Ugvz41OKCxOTUvNSSeBdvA3NLSwtLk5AQY2Ni1AAARqItXw</recordid><startdate>20040809</startdate><enddate>20040809</enddate><creator>EFFENBERGER, FRANZ, DR</creator><creator>ROOS, JUERGEN</creator><creator>WAJANT, HARALD</creator><creator>FOERSTER, SIEGFRIED</creator><scope>EVB</scope></search><sort><creationdate>20040809</creationdate><title>Fremgangsmåde til fremstilling af (S)-cyanhydriner</title><author>EFFENBERGER, FRANZ, DR ; ROOS, JUERGEN ; WAJANT, HARALD ; FOERSTER, SIEGFRIED</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DK0799894TT33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>dan</language><creationdate>2004</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>ORGANIC CHEMISTRY</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>EFFENBERGER, FRANZ, DR</creatorcontrib><creatorcontrib>ROOS, JUERGEN</creatorcontrib><creatorcontrib>WAJANT, HARALD</creatorcontrib><creatorcontrib>FOERSTER, SIEGFRIED</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>EFFENBERGER, FRANZ, DR</au><au>ROOS, JUERGEN</au><au>WAJANT, HARALD</au><au>FOERSTER, SIEGFRIED</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Fremgangsmåde til fremstilling af (S)-cyanhydriner</title><date>2004-08-09</date><risdate>2004</risdate><abstract>Preparation of (S)-cyanohydrin compounds of formula (I) comprises enzyme-catalysed reaction of carbonyl compounds of formula (II) with hydrocyanic acid, or a substance which releases hydrocyanic acid or CN, in the presence of a catalytic amount of an (S)-oxynitrilase immobilised on a nitrocellulose carrier. R, R' = H; 1-18C alkyl, 2-18C alkenyl or 2-18C alkynyl (all optionally substituted by ≥ 1 amine, imine, OH, 1-6C alkoxy, halo, carboxyl, 3-20C cycloalkyl and/or Het substituents, where the cyclic substituents are themselves optionally substituted by ≥ 1 halo, OH, 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl); or a (hetero)aromatic group containing 5-22 ring atoms, in which up to 4 ring C atoms may be replaced by N, O and/or S atoms, the ring being optionally substituted by ≥ 1 amine, imine, OH, 1-8C alkoxy, aryloxy, halo, carboxy or 1-22C optionally unsaturated alkyl, where ≥ 2 of the ring substituents may combine to form a cyclic group; Het = an aromatic ring with up to 22C atoms which is optionally substituted by N, O or S heteroatoms; provided that R' and R are not both H.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | dan |
recordid | cdi_epo_espacenet_DK0799894TT3 |
source | esp@cenet |
subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE HETEROCYCLIC COMPOUNDS METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING ORGANIC CHEMISTRY PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS VINEGAR WINE |
title | Fremgangsmåde til fremstilling af (S)-cyanhydriner |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T02%3A03%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=EFFENBERGER,%20FRANZ,%20DR&rft.date=2004-08-09&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDK0799894TT3%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |