Loading…

A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates

An efficient coupling of terminal alkynes and CO(2) in the presence of alkyl halides can be achieved under ambient conditions using a copper/phosphine catalyst system, providing facile access to a variety of functionalised alkyl 2-alkynoates.

Saved in:
Bibliographic Details
Published in:Organic & biomolecular chemistry 2012-02, Vol.10 (8), p.1514-1516
Main Authors: Inamoto, Kiyofumi, Asano, Narumi, Kobayashi, Koji, Yonemoto, Misato, Kondo, Yoshinori
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003
cites cdi_FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003
container_end_page 1516
container_issue 8
container_start_page 1514
container_title Organic & biomolecular chemistry
container_volume 10
creator Inamoto, Kiyofumi
Asano, Narumi
Kobayashi, Koji
Yonemoto, Misato
Kondo, Yoshinori
description An efficient coupling of terminal alkynes and CO(2) in the presence of alkyl halides can be achieved under ambient conditions using a copper/phosphine catalyst system, providing facile access to a variety of functionalised alkyl 2-alkynoates.
doi_str_mv 10.1039/c2ob06884b
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_919955443</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>919955443</sourcerecordid><originalsourceid>FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003</originalsourceid><addsrcrecordid>eNpFkEtLw0AUhQdRrFY3_gDJThCi80wy7krxBQU3ug7zuMHoJBNnpmD-vamtdXUP53wcuAehC4JvCGby1lCvcVFVXB-gE8LLMseCycO9pniGTmP8wJjIsuDHaEYpZbxgxQlqFpnxwwAh1yqCzYxKyo2pNVkcY4Iua3yYzKD99-hUan2f-SZLELq2Vy5T7nPsId5NdJ_eIbZxE29cl9H8N_UqQTxDR41yEc53d47eHu5fl0_56uXxeblY5YYJmnLCreS4NEBACyCywsBKIVlZNFZSwawxGoTRk8TWcmqZorqSxfSYtoAxm6Orbe8Q_NcaYqq7NhpwTvXg17GWREohOGcTeb0lTfAxBmjqIbSdCmNNcL2Ztf6fdYIvd7Vr3YHdo387sh9Rp3Rr</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>919955443</pqid></control><display><type>article</type><title>A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates</title><source>Royal Society of Chemistry</source><creator>Inamoto, Kiyofumi ; Asano, Narumi ; Kobayashi, Koji ; Yonemoto, Misato ; Kondo, Yoshinori</creator><creatorcontrib>Inamoto, Kiyofumi ; Asano, Narumi ; Kobayashi, Koji ; Yonemoto, Misato ; Kondo, Yoshinori</creatorcontrib><description>An efficient coupling of terminal alkynes and CO(2) in the presence of alkyl halides can be achieved under ambient conditions using a copper/phosphine catalyst system, providing facile access to a variety of functionalised alkyl 2-alkynoates.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c2ob06884b</identifier><identifier>PMID: 22234636</identifier><language>eng</language><publisher>England</publisher><subject>Alkynes - chemistry ; Carbon Dioxide - chemistry ; Catalysis ; Copper - chemistry ; Molecular Structure</subject><ispartof>Organic &amp; biomolecular chemistry, 2012-02, Vol.10 (8), p.1514-1516</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003</citedby><cites>FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22234636$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inamoto, Kiyofumi</creatorcontrib><creatorcontrib>Asano, Narumi</creatorcontrib><creatorcontrib>Kobayashi, Koji</creatorcontrib><creatorcontrib>Yonemoto, Misato</creatorcontrib><creatorcontrib>Kondo, Yoshinori</creatorcontrib><title>A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates</title><title>Organic &amp; biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>An efficient coupling of terminal alkynes and CO(2) in the presence of alkyl halides can be achieved under ambient conditions using a copper/phosphine catalyst system, providing facile access to a variety of functionalised alkyl 2-alkynoates.</description><subject>Alkynes - chemistry</subject><subject>Carbon Dioxide - chemistry</subject><subject>Catalysis</subject><subject>Copper - chemistry</subject><subject>Molecular Structure</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLw0AUhQdRrFY3_gDJThCi80wy7krxBQU3ug7zuMHoJBNnpmD-vamtdXUP53wcuAehC4JvCGby1lCvcVFVXB-gE8LLMseCycO9pniGTmP8wJjIsuDHaEYpZbxgxQlqFpnxwwAh1yqCzYxKyo2pNVkcY4Iua3yYzKD99-hUan2f-SZLELq2Vy5T7nPsId5NdJ_eIbZxE29cl9H8N_UqQTxDR41yEc53d47eHu5fl0_56uXxeblY5YYJmnLCreS4NEBACyCywsBKIVlZNFZSwawxGoTRk8TWcmqZorqSxfSYtoAxm6Orbe8Q_NcaYqq7NhpwTvXg17GWREohOGcTeb0lTfAxBmjqIbSdCmNNcL2Ztf6fdYIvd7Vr3YHdo387sh9Rp3Rr</recordid><startdate>20120228</startdate><enddate>20120228</enddate><creator>Inamoto, Kiyofumi</creator><creator>Asano, Narumi</creator><creator>Kobayashi, Koji</creator><creator>Yonemoto, Misato</creator><creator>Kondo, Yoshinori</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120228</creationdate><title>A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates</title><author>Inamoto, Kiyofumi ; Asano, Narumi ; Kobayashi, Koji ; Yonemoto, Misato ; Kondo, Yoshinori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Alkynes - chemistry</topic><topic>Carbon Dioxide - chemistry</topic><topic>Catalysis</topic><topic>Copper - chemistry</topic><topic>Molecular Structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inamoto, Kiyofumi</creatorcontrib><creatorcontrib>Asano, Narumi</creatorcontrib><creatorcontrib>Kobayashi, Koji</creatorcontrib><creatorcontrib>Yonemoto, Misato</creatorcontrib><creatorcontrib>Kondo, Yoshinori</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic &amp; biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inamoto, Kiyofumi</au><au>Asano, Narumi</au><au>Kobayashi, Koji</au><au>Yonemoto, Misato</au><au>Kondo, Yoshinori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates</atitle><jtitle>Organic &amp; biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2012-02-28</date><risdate>2012</risdate><volume>10</volume><issue>8</issue><spage>1514</spage><epage>1516</epage><pages>1514-1516</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>An efficient coupling of terminal alkynes and CO(2) in the presence of alkyl halides can be achieved under ambient conditions using a copper/phosphine catalyst system, providing facile access to a variety of functionalised alkyl 2-alkynoates.</abstract><cop>England</cop><pmid>22234636</pmid><doi>10.1039/c2ob06884b</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1477-0520
ispartof Organic & biomolecular chemistry, 2012-02, Vol.10 (8), p.1514-1516
issn 1477-0520
1477-0539
language eng
recordid cdi_proquest_miscellaneous_919955443
source Royal Society of Chemistry
subjects Alkynes - chemistry
Carbon Dioxide - chemistry
Catalysis
Copper - chemistry
Molecular Structure
title A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T23%3A06%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20copper-based%20catalytic%20system%20for%20carboxylation%20of%20terminal%20alkynes:%20synthesis%20of%20alkyl%202-alkynoates&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=Inamoto,%20Kiyofumi&rft.date=2012-02-28&rft.volume=10&rft.issue=8&rft.spage=1514&rft.epage=1516&rft.pages=1514-1516&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/c2ob06884b&rft_dat=%3Cproquest_cross%3E919955443%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c352t-14d9407ce1eb5e1980e3759376fd9253dccbe5cb2530dd42d3a2b896019bde003%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=919955443&rft_id=info:pmid/22234636&rfr_iscdi=true