A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e
A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. This protocol was extended to the three-component process using alkyliden...
Gespeichert in:
Hauptverfasser: | , |
---|---|
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 5996 |
---|---|
container_issue | 45 |
container_start_page | 5993 |
container_title | |
container_volume | 5 |
creator | Kippo, Takashi Ryu, Ilhyong |
description | A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. This protocol was extended to the three-component process using alkylidenecyclopropane, which gave 2-bromo-1,8-diene along with alkylidenecyclopentane.
A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. |
doi_str_mv | 10.1039/c4cc01597e |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c4cc01597e</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c4cc01597e</sourcerecordid><originalsourceid>FETCH-rsc_primary_c4cc01597e3</originalsourceid><addsrcrecordid>eNqFUD1PwzAQDQgkysfCipCODaS6JCShHxuCIDoxlIGtutoXeuDYkW0Q_ffEpRIDEtxyp3vv3j29JDnO0kGW5uNLWUiZZuV4SNtJL8uvC1EWo-edOJdjMcyLci_Z9_417SorR72tkxtYONuwIeFQsUQNDSnGQArC0hEJaZvWGjIBHKEMbA3ElWPP5gVQazLk-0CaZHDWCEU1S4581G8RAzQq8lb6-5UiP4EaJWsCvzJhSZ492BquRMStyPpDoTieVhtRluDf21ZT0-miWwGb2roG127Oq9n0AvADWeNC0wSqz5Ycr6kaPH17jiZ8u5bz0radosKAA5gRwd3jdAK_IzxMdmvUno42_SA5va-ebh-E83LeBdB0TuY_9Px__OwvfN6qOv8C4gKUAQ</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Kippo, Takashi ; Ryu, Ilhyong</creator><creatorcontrib>Kippo, Takashi ; Ryu, Ilhyong</creatorcontrib><description>A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. This protocol was extended to the three-component process using alkylidenecyclopropane, which gave 2-bromo-1,8-diene along with alkylidenecyclopentane.
A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c4cc01597e</identifier><language>eng</language><creationdate>2014-05</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kippo, Takashi</creatorcontrib><creatorcontrib>Ryu, Ilhyong</creatorcontrib><title>A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e</title><description>A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. This protocol was extended to the three-component process using alkylidenecyclopropane, which gave 2-bromo-1,8-diene along with alkylidenecyclopentane.
A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUD1PwzAQDQgkysfCipCODaS6JCShHxuCIDoxlIGtutoXeuDYkW0Q_ffEpRIDEtxyp3vv3j29JDnO0kGW5uNLWUiZZuV4SNtJL8uvC1EWo-edOJdjMcyLci_Z9_417SorR72tkxtYONuwIeFQsUQNDSnGQArC0hEJaZvWGjIBHKEMbA3ElWPP5gVQazLk-0CaZHDWCEU1S4581G8RAzQq8lb6-5UiP4EaJWsCvzJhSZ492BquRMStyPpDoTieVhtRluDf21ZT0-miWwGb2roG127Oq9n0AvADWeNC0wSqz5Ycr6kaPH17jiZ8u5bz0radosKAA5gRwd3jdAK_IzxMdmvUno42_SA5va-ebh-E83LeBdB0TuY_9Px__OwvfN6qOv8C4gKUAQ</recordid><startdate>20140508</startdate><enddate>20140508</enddate><creator>Kippo, Takashi</creator><creator>Ryu, Ilhyong</creator><scope/></search><sort><creationdate>20140508</creationdate><title>A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e</title><author>Kippo, Takashi ; Ryu, Ilhyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c4cc01597e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kippo, Takashi</creatorcontrib><creatorcontrib>Ryu, Ilhyong</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kippo, Takashi</au><au>Ryu, Ilhyong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e</atitle><date>2014-05-08</date><risdate>2014</risdate><volume>5</volume><issue>45</issue><spage>5993</spage><epage>5996</epage><pages>5993-5996</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields. This protocol was extended to the three-component process using alkylidenecyclopropane, which gave 2-bromo-1,8-diene along with alkylidenecyclopentane.
A bromine-radical mediated three-component coupling reaction was effectively achieved by the use of allenes, electron-deficient alkenes, and allyl bromides and led to the synthesis of 2-bromo-1,7-dienes in good to high yields.</abstract><doi>10.1039/c4cc01597e</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | |
issn | 1359-7345 1364-548X |
language | eng |
recordid | cdi_rsc_primary_c4cc01597e |
source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
title | A bromine-radical mediated three-component reaction comprising allenes, electron-deficient alkenes and allyl bromides: facile synthesis of 2-bromo-1,7-dienesElectronic supplementary information (ESI) available: Experimental section and spectroscopic data. See DOI: 10.1039/c4cc01597e |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T08%3A32%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20bromine-radical%20mediated%20three-component%20reaction%20comprising%20allenes,%20electron-deficient%20alkenes%20and%20allyl%20bromides:%20facile%20synthesis%20of%202-bromo-1,7-dienesElectronic%20supplementary%20information%20(ESI)%20available:%20Experimental%20section%20and%20spectroscopic%20data.%20See%20DOI:%2010.1039/c4cc01597e&rft.au=Kippo,%20Takashi&rft.date=2014-05-08&rft.volume=5&rft.issue=45&rft.spage=5993&rft.epage=5996&rft.pages=5993-5996&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c4cc01597e&rft_dat=%3Crsc%3Ec4cc01597e%3C/rsc%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 |