Loading…

Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system

A straightforward method for the hydrophenoxylation of internal alkynes, using N-heterocyclic carbene-based copper(i) and gold(i) complexes, is described. The heterobimetallic catalytic system proceeds via dual activation of the substrates to afford the desired vinylether derivatives. This methodolo...

Full description

Saved in:
Bibliographic Details
Published in:Dalton transactions : an international journal of inorganic chemistry 2017-02, Vol.46 (8), p.2439-2444
Main Authors: Lazreg, Faïma, Guidone, Stefano, Gómez-Herrera, Alberto, Nahra, Fady, Cazin, Catherine S J
Format: Article
Language:English
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-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913
cites cdi_FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913
container_end_page 2444
container_issue 8
container_start_page 2439
container_title Dalton transactions : an international journal of inorganic chemistry
container_volume 46
creator Lazreg, Faïma
Guidone, Stefano
Gómez-Herrera, Alberto
Nahra, Fady
Cazin, Catherine S J
description A straightforward method for the hydrophenoxylation of internal alkynes, using N-heterocyclic carbene-based copper(i) and gold(i) complexes, is described. The heterobimetallic catalytic system proceeds via dual activation of the substrates to afford the desired vinylether derivatives. This methodology is shown to be highly efficient and tolerates a wide range of substituted phenols and alkynes.
doi_str_mv 10.1039/c6dt04513h
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1857752799</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1857752799</sourcerecordid><originalsourceid>FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913</originalsourceid><addsrcrecordid>eNo9kMtOwzAURC0EoqWw4QOQlwgp1I_EjpdVeBSpgk1Zosi1b5RAEpfYEeTvCaV0NSPN0SwOQpeU3FLC1dwIG0icUF4eoSmNpYwU4_HxoTMxQWfevxPCGEnYKZqwlMiYETJFb8vBdm5bQuu-h1qHyrXYFbhqA3StrrGuP4YWPDY66HrwYPFXFUqscQkj4TZVA-NQVwZnffS8zOaLXWA_-ADNOTopdO3hYp8z9Ppwv86W0erl8SlbrCLDUhkiKRLgheYxADFJwRIKKTFglCiAS2WFZGmheGqFlYZS0NSYVCpppUiFVJTP0PXf77Zznz34kDeVN1DXugXX-5ymiZQJk0qN6M0fajrnfQdFvu2qRndDTkn-qzPPxN16p3M5wlf7337TgD2g__74D8socFY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1857752799</pqid></control><display><type>article</type><title>Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system</title><source>Royal Society of Chemistry</source><creator>Lazreg, Faïma ; Guidone, Stefano ; Gómez-Herrera, Alberto ; Nahra, Fady ; Cazin, Catherine S J</creator><creatorcontrib>Lazreg, Faïma ; Guidone, Stefano ; Gómez-Herrera, Alberto ; Nahra, Fady ; Cazin, Catherine S J</creatorcontrib><description>A straightforward method for the hydrophenoxylation of internal alkynes, using N-heterocyclic carbene-based copper(i) and gold(i) complexes, is described. The heterobimetallic catalytic system proceeds via dual activation of the substrates to afford the desired vinylether derivatives. This methodology is shown to be highly efficient and tolerates a wide range of substituted phenols and alkynes.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c6dt04513h</identifier><identifier>PMID: 28074200</identifier><language>eng</language><publisher>England</publisher><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2017-02, Vol.46 (8), p.2439-2444</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913</citedby><cites>FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913</cites><orcidid>0000-0002-9094-8131</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28074200$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lazreg, Faïma</creatorcontrib><creatorcontrib>Guidone, Stefano</creatorcontrib><creatorcontrib>Gómez-Herrera, Alberto</creatorcontrib><creatorcontrib>Nahra, Fady</creatorcontrib><creatorcontrib>Cazin, Catherine S J</creatorcontrib><title>Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system</title><title>Dalton transactions : an international journal of inorganic chemistry</title><addtitle>Dalton Trans</addtitle><description>A straightforward method for the hydrophenoxylation of internal alkynes, using N-heterocyclic carbene-based copper(i) and gold(i) complexes, is described. The heterobimetallic catalytic system proceeds via dual activation of the substrates to afford the desired vinylether derivatives. This methodology is shown to be highly efficient and tolerates a wide range of substituted phenols and alkynes.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOwzAURC0EoqWw4QOQlwgp1I_EjpdVeBSpgk1Zosi1b5RAEpfYEeTvCaV0NSPN0SwOQpeU3FLC1dwIG0icUF4eoSmNpYwU4_HxoTMxQWfevxPCGEnYKZqwlMiYETJFb8vBdm5bQuu-h1qHyrXYFbhqA3StrrGuP4YWPDY66HrwYPFXFUqscQkj4TZVA-NQVwZnffS8zOaLXWA_-ADNOTopdO3hYp8z9Ppwv86W0erl8SlbrCLDUhkiKRLgheYxADFJwRIKKTFglCiAS2WFZGmheGqFlYZS0NSYVCpppUiFVJTP0PXf77Zznz34kDeVN1DXugXX-5ymiZQJk0qN6M0fajrnfQdFvu2qRndDTkn-qzPPxN16p3M5wlf7337TgD2g__74D8socFY</recordid><startdate>20170221</startdate><enddate>20170221</enddate><creator>Lazreg, Faïma</creator><creator>Guidone, Stefano</creator><creator>Gómez-Herrera, Alberto</creator><creator>Nahra, Fady</creator><creator>Cazin, Catherine S J</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9094-8131</orcidid></search><sort><creationdate>20170221</creationdate><title>Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system</title><author>Lazreg, Faïma ; Guidone, Stefano ; Gómez-Herrera, Alberto ; Nahra, Fady ; Cazin, Catherine S J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lazreg, Faïma</creatorcontrib><creatorcontrib>Guidone, Stefano</creatorcontrib><creatorcontrib>Gómez-Herrera, Alberto</creatorcontrib><creatorcontrib>Nahra, Fady</creatorcontrib><creatorcontrib>Cazin, Catherine S J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lazreg, Faïma</au><au>Guidone, Stefano</au><au>Gómez-Herrera, Alberto</au><au>Nahra, Fady</au><au>Cazin, Catherine S J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><addtitle>Dalton Trans</addtitle><date>2017-02-21</date><risdate>2017</risdate><volume>46</volume><issue>8</issue><spage>2439</spage><epage>2444</epage><pages>2439-2444</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>A straightforward method for the hydrophenoxylation of internal alkynes, using N-heterocyclic carbene-based copper(i) and gold(i) complexes, is described. The heterobimetallic catalytic system proceeds via dual activation of the substrates to afford the desired vinylether derivatives. This methodology is shown to be highly efficient and tolerates a wide range of substituted phenols and alkynes.</abstract><cop>England</cop><pmid>28074200</pmid><doi>10.1039/c6dt04513h</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-9094-8131</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1477-9226
ispartof Dalton transactions : an international journal of inorganic chemistry, 2017-02, Vol.46 (8), p.2439-2444
issn 1477-9226
1477-9234
language eng
recordid cdi_proquest_miscellaneous_1857752799
source Royal Society of Chemistry
title Hydrophenoxylation of internal alkynes catalysed with a heterobimetallic Cu-NHC/Au-NHC system
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T23%3A46%3A17IST&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=Hydrophenoxylation%20of%20internal%20alkynes%20catalysed%20with%20a%20heterobimetallic%20Cu-NHC/Au-NHC%20system&rft.jtitle=Dalton%20transactions%20:%20an%20international%20journal%20of%20inorganic%20chemistry&rft.au=Lazreg,%20Fa%C3%AFma&rft.date=2017-02-21&rft.volume=46&rft.issue=8&rft.spage=2439&rft.epage=2444&rft.pages=2439-2444&rft.issn=1477-9226&rft.eissn=1477-9234&rft_id=info:doi/10.1039/c6dt04513h&rft_dat=%3Cproquest_cross%3E1857752799%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c287t-765e3fa34ee0c5f251e80cec96fe379d6728f938d6d7c11ea1cc8797d76867913%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1857752799&rft_id=info:pmid/28074200&rfr_iscdi=true