Iron/N-doped graphene nano-structured catalysts for general cyclopropanation of olefins† †Electronic supplementary information (ESI) available: Experimental details for catalyst preparation and catalytic reactions, additional catalytic results, catalyst characterisation, and cyclopropane characterisation. See DOI: 10.1039/d0sc01650k
An Fe-based heterogeneous catalyst allows for the synthesis of cyclopropanes via a carbene transfer reaction, a transformation usually belonging to the homogeneous domain. The first examples of heterogeneous Fe-catalysed cyclopropanation reactions are presented. Pyrolysis of in situ -generated iron/...
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creator | Sarkar, Abhijnan Formenti, Dario Ferretti, Francesco Kreyenschulte, Carsten Bartling, Stephan Junge, Kathrin Beller, Matthias Ragaini, Fabio |
description | An Fe-based heterogeneous catalyst allows for the synthesis of cyclopropanes
via
a carbene transfer reaction, a transformation usually belonging to the homogeneous domain.
The first examples of heterogeneous Fe-catalysed cyclopropanation reactions are presented. Pyrolysis of
in situ
-generated iron/phenanthroline complexes in the presence of a carbonaceous material leads to specific supported nanosized iron particles, which are effective catalysts for carbene transfer reactions. Using olefins as substrates, cyclopropanes are obtained in high yields and moderate diastereoselectivities. The developed protocol is scalable and the activity of the recycled catalyst after deactivation can be effectively restored using an oxidative reactivation protocol under mild conditions. |
doi_str_mv | 10.1039/d0sc01650k |
format | Article |
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via
a carbene transfer reaction, a transformation usually belonging to the homogeneous domain.
The first examples of heterogeneous Fe-catalysed cyclopropanation reactions are presented. Pyrolysis of
in situ
-generated iron/phenanthroline complexes in the presence of a carbonaceous material leads to specific supported nanosized iron particles, which are effective catalysts for carbene transfer reactions. Using olefins as substrates, cyclopropanes are obtained in high yields and moderate diastereoselectivities. The developed protocol is scalable and the activity of the recycled catalyst after deactivation can be effectively restored using an oxidative reactivation protocol under mild conditions.</description><identifier>ISSN: 2041-6520</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/d0sc01650k</identifier><identifier>PMID: 32953016</identifier><language>eng</language><publisher>Royal Society of Chemistry</publisher><subject>Chemistry</subject><ispartof>Chemical science (Cambridge), 2020-06, Vol.11 (24), p.6217-6221</ispartof><rights>This journal is © The Royal Society of Chemistry 2020 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480268/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480268/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Sarkar, Abhijnan</creatorcontrib><creatorcontrib>Formenti, Dario</creatorcontrib><creatorcontrib>Ferretti, Francesco</creatorcontrib><creatorcontrib>Kreyenschulte, Carsten</creatorcontrib><creatorcontrib>Bartling, Stephan</creatorcontrib><creatorcontrib>Junge, Kathrin</creatorcontrib><creatorcontrib>Beller, Matthias</creatorcontrib><creatorcontrib>Ragaini, Fabio</creatorcontrib><title>Iron/N-doped graphene nano-structured catalysts for general cyclopropanation of olefins† †Electronic supplementary information (ESI) available: Experimental details for catalyst preparation and catalytic reactions, additional catalytic results, catalyst characterisation, and cyclopropane characterisation. See DOI: 10.1039/d0sc01650k</title><title>Chemical science (Cambridge)</title><description>An Fe-based heterogeneous catalyst allows for the synthesis of cyclopropanes
via
a carbene transfer reaction, a transformation usually belonging to the homogeneous domain.
The first examples of heterogeneous Fe-catalysed cyclopropanation reactions are presented. Pyrolysis of
in situ
-generated iron/phenanthroline complexes in the presence of a carbonaceous material leads to specific supported nanosized iron particles, which are effective catalysts for carbene transfer reactions. Using olefins as substrates, cyclopropanes are obtained in high yields and moderate diastereoselectivities. The developed protocol is scalable and the activity of the recycled catalyst after deactivation can be effectively restored using an oxidative reactivation protocol under mild conditions.</description><subject>Chemistry</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqlUU1PAjEQXY1GiXLxF8xRExa6u3wfvChGLpqI983QHaBa2qbtErn5U_xt_hILCGo42qTpZN6892amUXSRsHrCsl6jYI6zpN1ir4dRJWXNJG63st7RLk7ZaVR17oWFk2VJK-2cRKdZ2mtlgVU5eBparRoPcaENFTC1aGakCBQqHTtvS-5LGwCOHuXSeQcTbWEaSixK4EsutbHaoEIvtAI9AS1pIpT7fP-AcAeSuA8OgoMrjZE0J-XRLkGoIDTfsC4Ho-EV4AKFxLGkPgzeDFmxLpVQkA_AxnjbBhhLBu2Gjmrbnw82lpCv0q4GWBRiFa46_YW7UvqA7rT4LChxHxzdWrC2UfyZjfZK6jAigtvHYR_2_-E8Op6gdFT9fs-i67vB8819bMrxnAoexgrLy02YMGwi1yjyv4gSs3yqF3mn2WVpu5v9W-ALPD2-8g</recordid><startdate>20200608</startdate><enddate>20200608</enddate><creator>Sarkar, Abhijnan</creator><creator>Formenti, Dario</creator><creator>Ferretti, Francesco</creator><creator>Kreyenschulte, Carsten</creator><creator>Bartling, Stephan</creator><creator>Junge, Kathrin</creator><creator>Beller, Matthias</creator><creator>Ragaini, Fabio</creator><general>Royal Society of Chemistry</general><scope>5PM</scope></search><sort><creationdate>20200608</creationdate><title>Iron/N-doped graphene nano-structured catalysts for general cyclopropanation of olefins† †Electronic supplementary information (ESI) available: Experimental details for catalyst preparation and catalytic reactions, additional catalytic results, catalyst characterisation, and cyclopropane characterisation. See DOI: 10.1039/d0sc01650k</title><author>Sarkar, Abhijnan ; Formenti, Dario ; Ferretti, Francesco ; Kreyenschulte, Carsten ; Bartling, Stephan ; Junge, Kathrin ; Beller, Matthias ; Ragaini, Fabio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_74802683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarkar, Abhijnan</creatorcontrib><creatorcontrib>Formenti, Dario</creatorcontrib><creatorcontrib>Ferretti, Francesco</creatorcontrib><creatorcontrib>Kreyenschulte, Carsten</creatorcontrib><creatorcontrib>Bartling, Stephan</creatorcontrib><creatorcontrib>Junge, Kathrin</creatorcontrib><creatorcontrib>Beller, Matthias</creatorcontrib><creatorcontrib>Ragaini, Fabio</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarkar, Abhijnan</au><au>Formenti, Dario</au><au>Ferretti, Francesco</au><au>Kreyenschulte, Carsten</au><au>Bartling, Stephan</au><au>Junge, Kathrin</au><au>Beller, Matthias</au><au>Ragaini, Fabio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iron/N-doped graphene nano-structured catalysts for general cyclopropanation of olefins† †Electronic supplementary information (ESI) available: Experimental details for catalyst preparation and catalytic reactions, additional catalytic results, catalyst characterisation, and cyclopropane characterisation. See DOI: 10.1039/d0sc01650k</atitle><jtitle>Chemical science (Cambridge)</jtitle><date>2020-06-08</date><risdate>2020</risdate><volume>11</volume><issue>24</issue><spage>6217</spage><epage>6221</epage><pages>6217-6221</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>An Fe-based heterogeneous catalyst allows for the synthesis of cyclopropanes
via
a carbene transfer reaction, a transformation usually belonging to the homogeneous domain.
The first examples of heterogeneous Fe-catalysed cyclopropanation reactions are presented. Pyrolysis of
in situ
-generated iron/phenanthroline complexes in the presence of a carbonaceous material leads to specific supported nanosized iron particles, which are effective catalysts for carbene transfer reactions. Using olefins as substrates, cyclopropanes are obtained in high yields and moderate diastereoselectivities. The developed protocol is scalable and the activity of the recycled catalyst after deactivation can be effectively restored using an oxidative reactivation protocol under mild conditions.</abstract><pub>Royal Society of Chemistry</pub><pmid>32953016</pmid><doi>10.1039/d0sc01650k</doi><oa>free_for_read</oa></addata></record> |
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subjects | Chemistry |
title | Iron/N-doped graphene nano-structured catalysts for general cyclopropanation of olefins† †Electronic supplementary information (ESI) available: Experimental details for catalyst preparation and catalytic reactions, additional catalytic results, catalyst characterisation, and cyclopropane characterisation. See DOI: 10.1039/d0sc01650k |
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