Loading…
Amine Oxidation by Electrochemically Generated Peroxodicarbonate
Abstract The N -oxidation of tertiary amines was achieved by using electrochemically generated peroxodicarbonate solutions as sustainable oxidizers. The presence of EDTA and 2,2,2-trifluoroacetophenone as a mediator was found to be crucial for converting water-insoluble substrates. Various tertiary...
Saved in:
Published in: | Synlett 2022-09, Vol.33 (15), p.1527-1531 |
---|---|
Main Authors: | , , , , , |
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-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3 |
container_end_page | 1531 |
container_issue | 15 |
container_start_page | 1527 |
container_title | Synlett |
container_volume | 33 |
creator | Seitz, Ann-Katrin van Lingen, Tim Dyga, Marco Kohlpaintner, Philipp J. Waldvogel, Siegfried R. Gooßen, Lukas J. |
description | Abstract
The
N
-oxidation of tertiary amines was achieved by using electrochemically generated peroxodicarbonate solutions as sustainable oxidizers. The presence of EDTA and 2,2,2-trifluoroacetophenone as a mediator was found to be crucial for converting water-insoluble substrates. Various tertiary amines were converted into their corresponding
N
-oxides in yields of up to 98%. The scope includes economically important surfactants and potential platform oxidizers. |
doi_str_mv | 10.1055/a-1860-3405 |
format | article |
fullrecord | <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_a_1860_3405</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_a_1860_3405</sourcerecordid><originalsourceid>FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3</originalsourceid><addsrcrecordid>eNptj01Lw0AURQdRsFZX_oGsldF5mY8kO0upVSjUha6HN5MXmpJkZBKh-fcm1KWrC5fD5R7G7kE8gdD6GTnkRnCphL5gC1Ay46kozCVbiEIarlNQ1-ym749CgMoLsWAvq7buKNmf6hKHOnSJG5NNQ36IwR-orT02zZhsqaOIA5XJB8VwCuXURxe6qbplVxU2Pd395ZJ9vW4-1298t9--r1c77qHIB65AUJWS8i4rtcxAk9SuBK8MKTDoUsyVdB5FgaasqCpQOZoeVgiZdkByyR7Puz6Gvo9U2e9YtxhHC8LO8hbtLG9n-Yl-ONPDoaaW7DH8xG669y_8C5nXWuU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Amine Oxidation by Electrochemically Generated Peroxodicarbonate</title><source>Thieme Connect (journals)</source><creator>Seitz, Ann-Katrin ; van Lingen, Tim ; Dyga, Marco ; Kohlpaintner, Philipp J. ; Waldvogel, Siegfried R. ; Gooßen, Lukas J.</creator><creatorcontrib>Seitz, Ann-Katrin ; van Lingen, Tim ; Dyga, Marco ; Kohlpaintner, Philipp J. ; Waldvogel, Siegfried R. ; Gooßen, Lukas J.</creatorcontrib><description>Abstract
The
N
-oxidation of tertiary amines was achieved by using electrochemically generated peroxodicarbonate solutions as sustainable oxidizers. The presence of EDTA and 2,2,2-trifluoroacetophenone as a mediator was found to be crucial for converting water-insoluble substrates. Various tertiary amines were converted into their corresponding
N
-oxides in yields of up to 98%. The scope includes economically important surfactants and potential platform oxidizers.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/a-1860-3405</identifier><language>eng</language><publisher>Rüdigerstraße 14, 70469 Stuttgart, Germany: Georg Thieme Verlag KG</publisher><subject>letter</subject><ispartof>Synlett, 2022-09, Vol.33 (15), p.1527-1531</ispartof><rights>Thieme. All rights reserved</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3</citedby><cites>FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3</cites><orcidid>0000-0002-7949-9638</orcidid></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/a-1860-3405.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/a-1860-3405$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,778,782,3006,3007,27911,27912,54546,54547</link.rule.ids></links><search><creatorcontrib>Seitz, Ann-Katrin</creatorcontrib><creatorcontrib>van Lingen, Tim</creatorcontrib><creatorcontrib>Dyga, Marco</creatorcontrib><creatorcontrib>Kohlpaintner, Philipp J.</creatorcontrib><creatorcontrib>Waldvogel, Siegfried R.</creatorcontrib><creatorcontrib>Gooßen, Lukas J.</creatorcontrib><title>Amine Oxidation by Electrochemically Generated Peroxodicarbonate</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
The
N
-oxidation of tertiary amines was achieved by using electrochemically generated peroxodicarbonate solutions as sustainable oxidizers. The presence of EDTA and 2,2,2-trifluoroacetophenone as a mediator was found to be crucial for converting water-insoluble substrates. Various tertiary amines were converted into their corresponding
N
-oxides in yields of up to 98%. The scope includes economically important surfactants and potential platform oxidizers.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNptj01Lw0AURQdRsFZX_oGsldF5mY8kO0upVSjUha6HN5MXmpJkZBKh-fcm1KWrC5fD5R7G7kE8gdD6GTnkRnCphL5gC1Ay46kozCVbiEIarlNQ1-ym749CgMoLsWAvq7buKNmf6hKHOnSJG5NNQ36IwR-orT02zZhsqaOIA5XJB8VwCuXURxe6qbplVxU2Pd395ZJ9vW4-1298t9--r1c77qHIB65AUJWS8i4rtcxAk9SuBK8MKTDoUsyVdB5FgaasqCpQOZoeVgiZdkByyR7Puz6Gvo9U2e9YtxhHC8LO8hbtLG9n-Yl-ONPDoaaW7DH8xG669y_8C5nXWuU</recordid><startdate>20220916</startdate><enddate>20220916</enddate><creator>Seitz, Ann-Katrin</creator><creator>van Lingen, Tim</creator><creator>Dyga, Marco</creator><creator>Kohlpaintner, Philipp J.</creator><creator>Waldvogel, Siegfried R.</creator><creator>Gooßen, Lukas J.</creator><general>Georg Thieme Verlag KG</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-7949-9638</orcidid></search><sort><creationdate>20220916</creationdate><title>Amine Oxidation by Electrochemically Generated Peroxodicarbonate</title><author>Seitz, Ann-Katrin ; van Lingen, Tim ; Dyga, Marco ; Kohlpaintner, Philipp J. ; Waldvogel, Siegfried R. ; Gooßen, Lukas J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seitz, Ann-Katrin</creatorcontrib><creatorcontrib>van Lingen, Tim</creatorcontrib><creatorcontrib>Dyga, Marco</creatorcontrib><creatorcontrib>Kohlpaintner, Philipp J.</creatorcontrib><creatorcontrib>Waldvogel, Siegfried R.</creatorcontrib><creatorcontrib>Gooßen, Lukas J.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seitz, Ann-Katrin</au><au>van Lingen, Tim</au><au>Dyga, Marco</au><au>Kohlpaintner, Philipp J.</au><au>Waldvogel, Siegfried R.</au><au>Gooßen, Lukas J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amine Oxidation by Electrochemically Generated Peroxodicarbonate</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2022-09-16</date><risdate>2022</risdate><volume>33</volume><issue>15</issue><spage>1527</spage><epage>1531</epage><pages>1527-1531</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
The
N
-oxidation of tertiary amines was achieved by using electrochemically generated peroxodicarbonate solutions as sustainable oxidizers. The presence of EDTA and 2,2,2-trifluoroacetophenone as a mediator was found to be crucial for converting water-insoluble substrates. Various tertiary amines were converted into their corresponding
N
-oxides in yields of up to 98%. The scope includes economically important surfactants and potential platform oxidizers.</abstract><cop>Rüdigerstraße 14, 70469 Stuttgart, Germany</cop><pub>Georg Thieme Verlag KG</pub><doi>10.1055/a-1860-3405</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-7949-9638</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0936-5214 |
ispartof | Synlett, 2022-09, Vol.33 (15), p.1527-1531 |
issn | 0936-5214 1437-2096 |
language | eng |
recordid | cdi_crossref_primary_10_1055_a_1860_3405 |
source | Thieme Connect (journals) |
subjects | letter |
title | Amine Oxidation by Electrochemically Generated Peroxodicarbonate |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T09%3A40%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amine%20Oxidation%20by%20Electrochemically%20Generated%20Peroxodicarbonate&rft.jtitle=Synlett&rft.au=Seitz,%20Ann-Katrin&rft.date=2022-09-16&rft.volume=33&rft.issue=15&rft.spage=1527&rft.epage=1531&rft.pages=1527-1531&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/a-1860-3405&rft_dat=%3Cthieme_cross%3E10_1055_a_1860_3405%3C/thieme_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c198t-410ef2e4cb7d53715e35bd1c46e416ab2a843bca09a6dfef9a4be890fa175b1e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |