1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet

1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet

Stereoconservative method for preparation of an (R)- or (S)-isomer of the compound of the formula I with at least 95% optical purity wherein R is a hydrogen atom, a saturated or unsaturated lower alkyl group, a cycloalkyl group, or a group (CH2)m Ph wherein m is O-3 and Ph is a substituted or unsubs...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: STROEM,HANS ERIC PETER, RAEMSBY,STEN INGVAR, HOEGBERG,THOMAS, FEDERSEL,HANS-JUERGEN
Format: Patent
Sprache:fin ; swe
Schlagworte:
APPARATUS THEREFOR
CHEMISTRY
GENERAL METHODS OF ORGANIC CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
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 STROEM,HANS ERIC PETER
RAEMSBY,STEN INGVAR
HOEGBERG,THOMAS
FEDERSEL,HANS-JUERGEN
description Stereoconservative method for preparation of an (R)- or (S)-isomer of the compound of the formula I with at least 95% optical purity wherein R is a hydrogen atom, a saturated or unsaturated lower alkyl group, a cycloalkyl group, or a group (CH2)m Ph wherein m is O-3 and Ph is a substituted or unsubstituted phenyl group including l) O,N-dialkylation, directly or stepwise of (R)- or (S)-proline 2) aminolysis 3) reduction to formation of the (R)- or (S)-isomer of the compound of the formula I, and new intermediates II and III in optical active form obtained by the reaction steps above and wherein R is defined as R above. h
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_FI95028CC</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>FI95028CC</sourcerecordid><originalsourceid>FETCH-epo_espacenet_FI95028CC3</originalsourceid><addsrcrecordid>eNqFjTEKwkAURNNYiHoF2TIBFzQiaB0M2qp9WPWLP9nshv0_wt7Ag-QmuZgbsLCzGIaZeTDj6L2S1F6JkVsbVIIR8TmRolQiPiUylapGY2tg7zU23jmr8Y5oMIAMT1spWghicGCdqsAwhIH6DrVn7rtX3wnyQ0soCKqfaEQY9fDLIfM0Gj2UJph9fRLN8_0lO0hobAHUqBsY4CI_7jbLdJtl67_AB6mzT0k</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet</title><source>esp@cenet</source><creator>STROEM,HANS ERIC PETER ; RAEMSBY,STEN INGVAR ; HOEGBERG,THOMAS ; FEDERSEL,HANS-JUERGEN</creator><creatorcontrib>STROEM,HANS ERIC PETER ; RAEMSBY,STEN INGVAR ; HOEGBERG,THOMAS ; FEDERSEL,HANS-JUERGEN</creatorcontrib><description>Stereoconservative method for preparation of an (R)- or (S)-isomer of the compound of the formula I with at least 95% optical purity wherein R is a hydrogen atom, a saturated or unsaturated lower alkyl group, a cycloalkyl group, or a group (CH2)m Ph wherein m is O-3 and Ph is a substituted or unsubstituted phenyl group including l) O,N-dialkylation, directly or stepwise of (R)- or (S)-proline 2) aminolysis 3) reduction to formation of the (R)- or (S)-isomer of the compound of the formula I, and new intermediates II and III in optical active form obtained by the reaction steps above and wherein R is defined as R above. h</description><edition>4</edition><language>fin ; swe</language><subject>APPARATUS THEREFOR ; CHEMISTRY ; GENERAL METHODS OF ORGANIC CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1995</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=19951211&amp;DB=EPODOC&amp;CC=FI&amp;NR=95028C$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19951211&amp;DB=EPODOC&amp;CC=FI&amp;NR=95028C$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>STROEM,HANS ERIC PETER</creatorcontrib><creatorcontrib>RAEMSBY,STEN INGVAR</creatorcontrib><creatorcontrib>HOEGBERG,THOMAS</creatorcontrib><creatorcontrib>FEDERSEL,HANS-JUERGEN</creatorcontrib><title>1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet</title><description>Stereoconservative method for preparation of an (R)- or (S)-isomer of the compound of the formula I with at least 95% optical purity wherein R is a hydrogen atom, a saturated or unsaturated lower alkyl group, a cycloalkyl group, or a group (CH2)m Ph wherein m is O-3 and Ph is a substituted or unsubstituted phenyl group including l) O,N-dialkylation, directly or stepwise of (R)- or (S)-proline 2) aminolysis 3) reduction to formation of the (R)- or (S)-isomer of the compound of the formula I, and new intermediates II and III in optical active form obtained by the reaction steps above and wherein R is defined as R above. h</description><subject>APPARATUS THEREFOR</subject><subject>CHEMISTRY</subject><subject>GENERAL METHODS OF ORGANIC CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1995</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFjTEKwkAURNNYiHoF2TIBFzQiaB0M2qp9WPWLP9nshv0_wt7Ag-QmuZgbsLCzGIaZeTDj6L2S1F6JkVsbVIIR8TmRolQiPiUylapGY2tg7zU23jmr8Y5oMIAMT1spWghicGCdqsAwhIH6DrVn7rtX3wnyQ0soCKqfaEQY9fDLIfM0Gj2UJph9fRLN8_0lO0hobAHUqBsY4CI_7jbLdJtl67_AB6mzT0k</recordid><startdate>19951211</startdate><enddate>19951211</enddate><creator>STROEM,HANS ERIC PETER</creator><creator>RAEMSBY,STEN INGVAR</creator><creator>HOEGBERG,THOMAS</creator><creator>FEDERSEL,HANS-JUERGEN</creator><scope>EVB</scope></search><sort><creationdate>19951211</creationdate><title>1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet</title><author>STROEM,HANS ERIC PETER ; RAEMSBY,STEN INGVAR ; HOEGBERG,THOMAS ; FEDERSEL,HANS-JUERGEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_FI95028CC3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>fin ; swe</language><creationdate>1995</creationdate><topic>APPARATUS THEREFOR</topic><topic>CHEMISTRY</topic><topic>GENERAL METHODS OF ORGANIC CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>STROEM,HANS ERIC PETER</creatorcontrib><creatorcontrib>RAEMSBY,STEN INGVAR</creatorcontrib><creatorcontrib>HOEGBERG,THOMAS</creatorcontrib><creatorcontrib>FEDERSEL,HANS-JUERGEN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>STROEM,HANS ERIC PETER</au><au>RAEMSBY,STEN INGVAR</au><au>HOEGBERG,THOMAS</au><au>FEDERSEL,HANS-JUERGEN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet</title><date>1995-12-11</date><risdate>1995</risdate><abstract>Stereoconservative method for preparation of an (R)- or (S)-isomer of the compound of the formula I with at least 95% optical purity wherein R is a hydrogen atom, a saturated or unsaturated lower alkyl group, a cycloalkyl group, or a group (CH2)m Ph wherein m is O-3 and Ph is a substituted or unsubstituted phenyl group including l) O,N-dialkylation, directly or stepwise of (R)- or (S)-proline 2) aminolysis 3) reduction to formation of the (R)- or (S)-isomer of the compound of the formula I, and new intermediates II and III in optical active form obtained by the reaction steps above and wherein R is defined as R above. h</abstract><edition>4</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language fin ; swe
recordid cdi_epo_espacenet_FI95028CC
source esp@cenet
subjects APPARATUS THEREFOR
CHEMISTRY
GENERAL METHODS OF ORGANIC CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title 1-substituoitujen (S)- ja (R)-2-aminometyylipyrrolidiinien tehokas, stereorakenteen säilyttävä synteesi sekä synteesin välituotteet
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T04%3A08%3A35IST&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=STROEM,HANS%20ERIC%20PETER&rft.date=1995-12-11&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EFI95028CC%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