PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL

Racemic or optically active 1-amino-4-(hydroxymethyl)-2- cyclopentene derivatives are obtained by acylation of 1-amino-2-cyclopentene-4- carboxylic acid with an acid halide, followed by reduction of the carboxyl group. A method for the production of racemic or optically active 4-(hydroxymethyl)-2-cy...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: BURGDORF KURT, ETTER KAY-SARA, DUC LAURENT DR, BRIEDEN WALTER DR, BERNEGGER CHRISTINE DR, BOSSARD PIERRE DR, URBAN EVA MARIA, BIRCH OLWEN MARY DR, BRUX FRANK, O MURCHU COLM DR, GUGGISBERG YVES DR, GORDON JOHN
Format: Patent
Sprache:cze ; eng
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 BURGDORF KURT
ETTER KAY-SARA
DUC LAURENT DR
BRIEDEN WALTER DR
BERNEGGER CHRISTINE DR
BOSSARD PIERRE DR
URBAN EVA MARIA
BIRCH OLWEN MARY DR
BRUX FRANK
O MURCHU COLM DR
GUGGISBERG YVES DR
GORDON JOHN
description Racemic or optically active 1-amino-4-(hydroxymethyl)-2- cyclopentene derivatives are obtained by acylation of 1-amino-2-cyclopentene-4- carboxylic acid with an acid halide, followed by reduction of the carboxyl group. A method for the production of racemic or optically active 4-(hydroxymethyl)-2-cyclopentene derivatives of formula (XIII) involves acylation of a cyclopentene-4-carboxylic acid derivative of formula (XIV) (as the racemate or an optically active isomer) with a carboxylic acid halide of formula R1>-CO-X (XI), followed by reduction of the resulting acid derivative (XV): [Image] R1>1-4C alkyl, 1-4C alkoxy, aryl or aryloxy; X : halogen.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CZ145898A3</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CZ145898A3</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CZ145898A33</originalsourceid><addsrcrecordid>eNqFi7EOgjAURVkcjPoNdiwJbyhUA2PTFEssbfOKAy6EmOpilAT_PzK4O92Tk3PXycOjkyoEUjskHpUX2NgToSxkHFMgi6UMMx5S4EBzEG1jHRxBauPQQQUa_GW5LNSbFHKQ_dk4r2ynrAIGreq0sM5sk9V9fM5x99tNsq9VJzXE6T3EeRpv8RU_g7wyfiirUhTF_-ILAOcyrw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL</title><source>esp@cenet</source><creator>BURGDORF KURT ; ETTER KAY-SARA ; DUC LAURENT DR ; BRIEDEN WALTER DR ; BERNEGGER CHRISTINE DR ; BOSSARD PIERRE DR ; URBAN EVA MARIA ; BIRCH OLWEN MARY DR ; BRUX FRANK ; O MURCHU COLM DR ; GUGGISBERG YVES DR ; GORDON JOHN</creator><creatorcontrib>BURGDORF KURT ; ETTER KAY-SARA ; DUC LAURENT DR ; BRIEDEN WALTER DR ; BERNEGGER CHRISTINE DR ; BOSSARD PIERRE DR ; URBAN EVA MARIA ; BIRCH OLWEN MARY DR ; BRUX FRANK ; O MURCHU COLM DR ; GUGGISBERG YVES DR ; GORDON JOHN</creatorcontrib><description>Racemic or optically active 1-amino-4-(hydroxymethyl)-2- cyclopentene derivatives are obtained by acylation of 1-amino-2-cyclopentene-4- carboxylic acid with an acid halide, followed by reduction of the carboxyl group. A method for the production of racemic or optically active 4-(hydroxymethyl)-2-cyclopentene derivatives of formula (XIII) involves acylation of a cyclopentene-4-carboxylic acid derivative of formula (XIV) (as the racemate or an optically active isomer) with a carboxylic acid halide of formula R1&gt;-CO-X (XI), followed by reduction of the resulting acid derivative (XV): [Image] R1&gt;1-4C alkyl, 1-4C alkoxy, aryl or aryloxy; X : halogen.</description><edition>6</edition><language>cze ; eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; BEER ; BIOCHEMISTRY ; CHEMISTRY ; 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 ; MUTATION OR GENETIC ENGINEERING ; ORGANIC CHEMISTRY ; PROCESSES USING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>1998</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&amp;date=19981216&amp;DB=EPODOC&amp;CC=CZ&amp;NR=145898A3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19981216&amp;DB=EPODOC&amp;CC=CZ&amp;NR=145898A3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BURGDORF KURT</creatorcontrib><creatorcontrib>ETTER KAY-SARA</creatorcontrib><creatorcontrib>DUC LAURENT DR</creatorcontrib><creatorcontrib>BRIEDEN WALTER DR</creatorcontrib><creatorcontrib>BERNEGGER CHRISTINE DR</creatorcontrib><creatorcontrib>BOSSARD PIERRE DR</creatorcontrib><creatorcontrib>URBAN EVA MARIA</creatorcontrib><creatorcontrib>BIRCH OLWEN MARY DR</creatorcontrib><creatorcontrib>BRUX FRANK</creatorcontrib><creatorcontrib>O MURCHU COLM DR</creatorcontrib><creatorcontrib>GUGGISBERG YVES DR</creatorcontrib><creatorcontrib>GORDON JOHN</creatorcontrib><title>PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL</title><description>Racemic or optically active 1-amino-4-(hydroxymethyl)-2- cyclopentene derivatives are obtained by acylation of 1-amino-2-cyclopentene-4- carboxylic acid with an acid halide, followed by reduction of the carboxyl group. A method for the production of racemic or optically active 4-(hydroxymethyl)-2-cyclopentene derivatives of formula (XIII) involves acylation of a cyclopentene-4-carboxylic acid derivative of formula (XIV) (as the racemate or an optically active isomer) with a carboxylic acid halide of formula R1&gt;-CO-X (XI), followed by reduction of the resulting acid derivative (XV): [Image] R1&gt;1-4C alkyl, 1-4C alkoxy, aryl or aryloxy; X : halogen.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</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>MUTATION OR GENETIC ENGINEERING</subject><subject>ORGANIC CHEMISTRY</subject><subject>PROCESSES USING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1998</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFi7EOgjAURVkcjPoNdiwJbyhUA2PTFEssbfOKAy6EmOpilAT_PzK4O92Tk3PXycOjkyoEUjskHpUX2NgToSxkHFMgi6UMMx5S4EBzEG1jHRxBauPQQQUa_GW5LNSbFHKQ_dk4r2ynrAIGreq0sM5sk9V9fM5x99tNsq9VJzXE6T3EeRpv8RU_g7wyfiirUhTF_-ILAOcyrw</recordid><startdate>19981216</startdate><enddate>19981216</enddate><creator>BURGDORF KURT</creator><creator>ETTER KAY-SARA</creator><creator>DUC LAURENT DR</creator><creator>BRIEDEN WALTER DR</creator><creator>BERNEGGER CHRISTINE DR</creator><creator>BOSSARD PIERRE DR</creator><creator>URBAN EVA MARIA</creator><creator>BIRCH OLWEN MARY DR</creator><creator>BRUX FRANK</creator><creator>O MURCHU COLM DR</creator><creator>GUGGISBERG YVES DR</creator><creator>GORDON JOHN</creator><scope>EVB</scope></search><sort><creationdate>19981216</creationdate><title>PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL</title><author>BURGDORF KURT ; ETTER KAY-SARA ; DUC LAURENT DR ; BRIEDEN WALTER DR ; BERNEGGER CHRISTINE DR ; BOSSARD PIERRE DR ; URBAN EVA MARIA ; BIRCH OLWEN MARY DR ; BRUX FRANK ; O MURCHU COLM DR ; GUGGISBERG YVES DR ; GORDON JOHN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CZ145898A33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>cze ; eng</language><creationdate>1998</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</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>MUTATION OR GENETIC ENGINEERING</topic><topic>ORGANIC CHEMISTRY</topic><topic>PROCESSES USING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>BURGDORF KURT</creatorcontrib><creatorcontrib>ETTER KAY-SARA</creatorcontrib><creatorcontrib>DUC LAURENT DR</creatorcontrib><creatorcontrib>BRIEDEN WALTER DR</creatorcontrib><creatorcontrib>BERNEGGER CHRISTINE DR</creatorcontrib><creatorcontrib>BOSSARD PIERRE DR</creatorcontrib><creatorcontrib>URBAN EVA MARIA</creatorcontrib><creatorcontrib>BIRCH OLWEN MARY DR</creatorcontrib><creatorcontrib>BRUX FRANK</creatorcontrib><creatorcontrib>O MURCHU COLM DR</creatorcontrib><creatorcontrib>GUGGISBERG YVES DR</creatorcontrib><creatorcontrib>GORDON JOHN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BURGDORF KURT</au><au>ETTER KAY-SARA</au><au>DUC LAURENT DR</au><au>BRIEDEN WALTER DR</au><au>BERNEGGER CHRISTINE DR</au><au>BOSSARD PIERRE DR</au><au>URBAN EVA MARIA</au><au>BIRCH OLWEN MARY DR</au><au>BRUX FRANK</au><au>O MURCHU COLM DR</au><au>GUGGISBERG YVES DR</au><au>GORDON JOHN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL</title><date>1998-12-16</date><risdate>1998</risdate><abstract>Racemic or optically active 1-amino-4-(hydroxymethyl)-2- cyclopentene derivatives are obtained by acylation of 1-amino-2-cyclopentene-4- carboxylic acid with an acid halide, followed by reduction of the carboxyl group. A method for the production of racemic or optically active 4-(hydroxymethyl)-2-cyclopentene derivatives of formula (XIII) involves acylation of a cyclopentene-4-carboxylic acid derivative of formula (XIV) (as the racemate or an optically active isomer) with a carboxylic acid halide of formula R1&gt;-CO-X (XI), followed by reduction of the resulting acid derivative (XV): [Image] R1&gt;1-4C alkyl, 1-4C alkoxy, aryl or aryloxy; X : halogen.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language cze ; eng
recordid cdi_epo_espacenet_CZ145898A3
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
BEER
BIOCHEMISTRY
CHEMISTRY
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
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
PROCESSES USING MICROORGANISMS
SPIRITS
VINEGAR
WINE
title PROCESS FOR PREPARING (1S,4R)- OR (1R,4S)-4-(2-AMINO-6-CHLORO-9-H-PURIN-9-YL)-2-CYKLOPENTENE-1-METHANOL
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A35%3A00IST&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=BURGDORF%20KURT&rft.date=1998-12-16&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECZ145898A3%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