Modified pictet-spengler reaction and products prepared therefrom
A method of introducing a second stereogenic center into a tetrahydro-beta-carboline have two stereogenic centers using a modified Pictet-Spengler reaction is disclosed. The method provides a desired cis- or trans-isomer in high yield and purity, and in short processes times.
Gespeichert in:
Hauptverfasser: | , , , , |
---|---|
Format: | Patent |
Sprache: | 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 | PAWLAK JOSEPH MATTHEW MARTINELLI MICHAEL JOHN ORME MARK W CHELIUS ERIK CHRISTOPHER DOECKE CHRISTOPHER WILLIAM |
description | A method of introducing a second stereogenic center into a tetrahydro-beta-carboline have two stereogenic centers using a modified Pictet-Spengler reaction is disclosed. The method provides a desired cis- or trans-isomer in high yield and purity, and in short processes times. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN1671706A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN1671706A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN1671706A3</originalsourceid><addsrcrecordid>eNrjZHD0zU_JTMtMTVEoyEwuSS3RLS5IzUvPSS1SKEpNTC7JzM9TSMwDShblp5QmlxQDGakFiUVA5SUZqUWpaUX5uTwMrGmJOcWpvFCam0HezTXE2UM3tSA_PrW4IDE5NS-1JN7Zz9DM3NDcwMzRmLAKAIE3MW4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Modified pictet-spengler reaction and products prepared therefrom</title><source>esp@cenet</source><creator>PAWLAK JOSEPH MATTHEW ; MARTINELLI MICHAEL JOHN ; ORME MARK W ; CHELIUS ERIK CHRISTOPHER ; DOECKE CHRISTOPHER WILLIAM</creator><creatorcontrib>PAWLAK JOSEPH MATTHEW ; MARTINELLI MICHAEL JOHN ; ORME MARK W ; CHELIUS ERIK CHRISTOPHER ; DOECKE CHRISTOPHER WILLIAM</creatorcontrib><description>A method of introducing a second stereogenic center into a tetrahydro-beta-carboline have two stereogenic centers using a modified Pictet-Spengler reaction is disclosed. The method provides a desired cis- or trans-isomer in high yield and purity, and in short processes times.</description><edition>7</edition><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2005</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=20050921&DB=EPODOC&CC=CN&NR=1671706A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20050921&DB=EPODOC&CC=CN&NR=1671706A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>PAWLAK JOSEPH MATTHEW</creatorcontrib><creatorcontrib>MARTINELLI MICHAEL JOHN</creatorcontrib><creatorcontrib>ORME MARK W</creatorcontrib><creatorcontrib>CHELIUS ERIK CHRISTOPHER</creatorcontrib><creatorcontrib>DOECKE CHRISTOPHER WILLIAM</creatorcontrib><title>Modified pictet-spengler reaction and products prepared therefrom</title><description>A method of introducing a second stereogenic center into a tetrahydro-beta-carboline have two stereogenic centers using a modified Pictet-Spengler reaction is disclosed. The method provides a desired cis- or trans-isomer in high yield and purity, and in short processes times.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHD0zU_JTMtMTVEoyEwuSS3RLS5IzUvPSS1SKEpNTC7JzM9TSMwDShblp5QmlxQDGakFiUVA5SUZqUWpaUX5uTwMrGmJOcWpvFCam0HezTXE2UM3tSA_PrW4IDE5NS-1JN7Zz9DM3NDcwMzRmLAKAIE3MW4</recordid><startdate>20050921</startdate><enddate>20050921</enddate><creator>PAWLAK JOSEPH MATTHEW</creator><creator>MARTINELLI MICHAEL JOHN</creator><creator>ORME MARK W</creator><creator>CHELIUS ERIK CHRISTOPHER</creator><creator>DOECKE CHRISTOPHER WILLIAM</creator><scope>EVB</scope></search><sort><creationdate>20050921</creationdate><title>Modified pictet-spengler reaction and products prepared therefrom</title><author>PAWLAK JOSEPH MATTHEW ; MARTINELLI MICHAEL JOHN ; ORME MARK W ; CHELIUS ERIK CHRISTOPHER ; DOECKE CHRISTOPHER WILLIAM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN1671706A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2005</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>PAWLAK JOSEPH MATTHEW</creatorcontrib><creatorcontrib>MARTINELLI MICHAEL JOHN</creatorcontrib><creatorcontrib>ORME MARK W</creatorcontrib><creatorcontrib>CHELIUS ERIK CHRISTOPHER</creatorcontrib><creatorcontrib>DOECKE CHRISTOPHER WILLIAM</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>PAWLAK JOSEPH MATTHEW</au><au>MARTINELLI MICHAEL JOHN</au><au>ORME MARK W</au><au>CHELIUS ERIK CHRISTOPHER</au><au>DOECKE CHRISTOPHER WILLIAM</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Modified pictet-spengler reaction and products prepared therefrom</title><date>2005-09-21</date><risdate>2005</risdate><abstract>A method of introducing a second stereogenic center into a tetrahydro-beta-carboline have two stereogenic centers using a modified Pictet-Spengler reaction is disclosed. The method provides a desired cis- or trans-isomer in high yield and purity, and in short processes times.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng |
recordid | cdi_epo_espacenet_CN1671706A |
source | esp@cenet |
subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Modified pictet-spengler reaction and products prepared therefrom |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T20%3A37%3A36IST&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=PAWLAK%20JOSEPH%20MATTHEW&rft.date=2005-09-21&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN1671706A%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 |