A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis
Abstract A C 2 -symmetric nucleophilic catalyst, (R,R)-3,5-diferrocenyl-4-(2′,5′-dimethylpyrrolidino)pyridine, was synthesised in three steps from commercially available (S,S)-hexane-2,5-diol. Application to the kinetic resolution of secondary alcohols (0.5 mol% loading) resulted in selectivity fac...
Gespeichert in:
Veröffentlicht in: | Synlett 2007-03, Vol.2007 (5), p.0725-0728 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 0728 |
---|---|
container_issue | 5 |
container_start_page | 0725 |
container_title | Synlett |
container_volume | 2007 |
creator | Nguyen, Huy V. Motevalli, Majid Richards, Christopher J. |
description | Abstract
A C
2
-symmetric nucleophilic catalyst, (R,R)-3,5-diferrocenyl-4-(2′,5′-dimethylpyrrolidino)pyridine, was synthesised in three steps from commercially available (S,S)-hexane-2,5-diol. Application to the kinetic resolution of secondary alcohols (0.5 mol% loading) resulted in selectivity factors (S) of up to 6. |
doi_str_mv | 10.1055/s-2007-970764 |
format | Article |
fullrecord | <record><control><sourceid>thieme</sourceid><recordid>TN_cdi_thieme_journals_10_1055_s_2007_970764</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_2007_970764</sourcerecordid><originalsourceid>FETCH-LOGICAL-s1074-c19d95a9ca1189d992821a2247a26634dffbe72cd467f03bd4db06cdecf2eddf3</originalsourceid><addsrcrecordid>eNo9kE1LxDAYhIMoWFeP3vsDjL5J06Q5luIXrB-wepSSJm9ol34sTffQf2_LiqcZhmEGHkJuGdwzSNOHQDmAolqBkuKMREwkaom0PCcR6ETSlDNxSa5C2AMwkWmIyE8eF5zu5q7DaWxs_IaTadvBYo_0cx7HoW1c0w-HeVwV4_ejbXE41E27lAuzlOcwxX4Y4zz8j-zmfqoxNOGaXHjTBrz50w35fnr8Kl7o9uP5tci3NDBQglqmnU6NtoaxbLGaZ5wZzoUyXMpEOO8rVNw6IZWHpHLCVSCtQ-s5OueTDbk77U51gx2W--E49sthyaBc0ZShXNGUJzTJL4ELWPs</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis</title><source>Thieme Connect Journals</source><creator>Nguyen, Huy V. ; Motevalli, Majid ; Richards, Christopher J.</creator><creatorcontrib>Nguyen, Huy V. ; Motevalli, Majid ; Richards, Christopher J.</creatorcontrib><description>Abstract
A C
2
-symmetric nucleophilic catalyst, (R,R)-3,5-diferrocenyl-4-(2′,5′-dimethylpyrrolidino)pyridine, was synthesised in three steps from commercially available (S,S)-hexane-2,5-diol. Application to the kinetic resolution of secondary alcohols (0.5 mol% loading) resulted in selectivity factors (S) of up to 6.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2007-970764</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2007-03, Vol.2007 (5), p.0725-0728</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-970764.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2007-970764$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Nguyen, Huy V.</creatorcontrib><creatorcontrib>Motevalli, Majid</creatorcontrib><creatorcontrib>Richards, Christopher J.</creatorcontrib><title>A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
A C
2
-symmetric nucleophilic catalyst, (R,R)-3,5-diferrocenyl-4-(2′,5′-dimethylpyrrolidino)pyridine, was synthesised in three steps from commercially available (S,S)-hexane-2,5-diol. Application to the kinetic resolution of secondary alcohols (0.5 mol% loading) resulted in selectivity factors (S) of up to 6.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9kE1LxDAYhIMoWFeP3vsDjL5J06Q5luIXrB-wepSSJm9ol34sTffQf2_LiqcZhmEGHkJuGdwzSNOHQDmAolqBkuKMREwkaom0PCcR6ETSlDNxSa5C2AMwkWmIyE8eF5zu5q7DaWxs_IaTadvBYo_0cx7HoW1c0w-HeVwV4_ejbXE41E27lAuzlOcwxX4Y4zz8j-zmfqoxNOGaXHjTBrz50w35fnr8Kl7o9uP5tci3NDBQglqmnU6NtoaxbLGaZ5wZzoUyXMpEOO8rVNw6IZWHpHLCVSCtQ-s5OueTDbk77U51gx2W--E49sthyaBc0ZShXNGUJzTJL4ELWPs</recordid><startdate>20070316</startdate><enddate>20070316</enddate><creator>Nguyen, Huy V.</creator><creator>Motevalli, Majid</creator><creator>Richards, Christopher J.</creator><scope/></search><sort><creationdate>20070316</creationdate><title>A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis</title><author>Nguyen, Huy V. ; Motevalli, Majid ; Richards, Christopher J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s1074-c19d95a9ca1189d992821a2247a26634dffbe72cd467f03bd4db06cdecf2eddf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Huy V.</creatorcontrib><creatorcontrib>Motevalli, Majid</creatorcontrib><creatorcontrib>Richards, Christopher J.</creatorcontrib><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Huy V.</au><au>Motevalli, Majid</au><au>Richards, Christopher J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2007-03-16</date><risdate>2007</risdate><volume>2007</volume><issue>5</issue><spage>0725</spage><epage>0728</epage><pages>0725-0728</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
A C
2
-symmetric nucleophilic catalyst, (R,R)-3,5-diferrocenyl-4-(2′,5′-dimethylpyrrolidino)pyridine, was synthesised in three steps from commercially available (S,S)-hexane-2,5-diol. Application to the kinetic resolution of secondary alcohols (0.5 mol% loading) resulted in selectivity factors (S) of up to 6.</abstract><doi>10.1055/s-2007-970764</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0936-5214 |
ispartof | Synlett, 2007-03, Vol.2007 (5), p.0725-0728 |
issn | 0936-5214 1437-2096 |
language | eng |
recordid | cdi_thieme_journals_10_1055_s_2007_970764 |
source | Thieme Connect Journals |
subjects | letter |
title | A C2-Symmetric Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T22%3A22%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20C2-Symmetric%20Metallocene-Pyrrolidinopyridine%20Nucleophilic%20Catalyst%20for%20Asymmetric%20Synthesis&rft.jtitle=Synlett&rft.au=Nguyen,%20Huy%20V.&rft.date=2007-03-16&rft.volume=2007&rft.issue=5&rft.spage=0725&rft.epage=0728&rft.pages=0725-0728&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-2007-970764&rft_dat=%3Cthieme%3E10_1055_s_2007_970764%3C/thieme%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 |