Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones
A safe, practical and selective process for the aerobic oxidation of alcohols to aldehydes and ketones has been developed using an Ru catalyst in a continuous flow reactor. Benzylic and allylic alcohols are oxidised selectively to their corresponding aldehydes and ketones, including substrates conta...
Gespeichert in:
Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2010-01, Vol.12 (12), p.2157-2163 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2163 |
---|---|
container_issue | 12 |
container_start_page | 2157 |
container_title | Green chemistry : an international journal and green chemistry resource : GC |
container_volume | 12 |
creator | ZOTOVA, Natalia HELLGARDT, Klaus KELSALL, Geoffrey H JESSIMAN, Alan S HII, King Kuok |
description | A safe, practical and selective process for the aerobic oxidation of alcohols to aldehydes and ketones has been developed using an Ru catalyst in a continuous flow reactor. Benzylic and allylic alcohols are oxidised selectively to their corresponding aldehydes and ketones, including substrates containing N- and S-heteroatoms. The rate of turnover is compatible with that previously reported using batch or microchannel reactors under optimised conditions. A preliminary kinetic model is derived that is supported by experimental observations. Last but not least, tandem oxidation-olefination may be achieved without the need to isolate the alcohol intermediate or to switch solvent. |
doi_str_mv | 10.1039/c0gc00493f |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_907182714</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>907182714</sourcerecordid><originalsourceid>FETCH-LOGICAL-c432t-4e725c139089bdfdbf03a897df999091e53810a619e7a0d54393b17f46317d4d3</originalsourceid><addsrcrecordid>eNpFkE9LAzEUxIMoWKsXP0EuIgirySa7abxJ8R8UvOh5eZu82Gi6qclW7bd3taWe3jyYGZgfIaecXXIm9JVhr4YxqYXbIyMua1HoUrH9na7LQ3KU8xtjnKtajghOoYewzj5T31EX4tc17edIlwlM7w0ECp2lGQMO7ydSwBRbb2j89hZ6HzsaHYVg4jyGTPs4aIvztcX8F3zHPnaYj8mBg5DxZHvH5OXu9nn6UMye7h-nN7PCSFH2hURVVoYLzSa6tc62jgmYaGWd1pppjpWYcAY116iA2UoKLVqu3LCNKyutGJPzTe8yxY8V5r5Z-GwwBOgwrnKjmeKTUnE5OC82TpNizglds0x-AWndcNb8omz-UQ7ms20t5AGJS9AZn3eJUtQVG9iKH2zbdBI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>907182714</pqid></control><display><type>article</type><title>Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>ZOTOVA, Natalia ; HELLGARDT, Klaus ; KELSALL, Geoffrey H ; JESSIMAN, Alan S ; HII, King Kuok</creator><creatorcontrib>ZOTOVA, Natalia ; HELLGARDT, Klaus ; KELSALL, Geoffrey H ; JESSIMAN, Alan S ; HII, King Kuok</creatorcontrib><description>A safe, practical and selective process for the aerobic oxidation of alcohols to aldehydes and ketones has been developed using an Ru catalyst in a continuous flow reactor. Benzylic and allylic alcohols are oxidised selectively to their corresponding aldehydes and ketones, including substrates containing N- and S-heteroatoms. The rate of turnover is compatible with that previously reported using batch or microchannel reactors under optimised conditions. A preliminary kinetic model is derived that is supported by experimental observations. Last but not least, tandem oxidation-olefination may be achieved without the need to isolate the alcohol intermediate or to switch solvent.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c0gc00493f</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Applied sciences ; Chemical engineering ; Chemistry ; Exact sciences and technology ; Kinetics and mechanisms ; Organic chemistry ; Reactivity and mechanisms ; Reactors</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2010-01, Vol.12 (12), p.2157-2163</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-4e725c139089bdfdbf03a897df999091e53810a619e7a0d54393b17f46317d4d3</citedby><cites>FETCH-LOGICAL-c432t-4e725c139089bdfdbf03a897df999091e53810a619e7a0d54393b17f46317d4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23650926$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>ZOTOVA, Natalia</creatorcontrib><creatorcontrib>HELLGARDT, Klaus</creatorcontrib><creatorcontrib>KELSALL, Geoffrey H</creatorcontrib><creatorcontrib>JESSIMAN, Alan S</creatorcontrib><creatorcontrib>HII, King Kuok</creatorcontrib><title>Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>A safe, practical and selective process for the aerobic oxidation of alcohols to aldehydes and ketones has been developed using an Ru catalyst in a continuous flow reactor. Benzylic and allylic alcohols are oxidised selectively to their corresponding aldehydes and ketones, including substrates containing N- and S-heteroatoms. The rate of turnover is compatible with that previously reported using batch or microchannel reactors under optimised conditions. A preliminary kinetic model is derived that is supported by experimental observations. Last but not least, tandem oxidation-olefination may be achieved without the need to isolate the alcohol intermediate or to switch solvent.</description><subject>Applied sciences</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Kinetics and mechanisms</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><subject>Reactors</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNpFkE9LAzEUxIMoWKsXP0EuIgirySa7abxJ8R8UvOh5eZu82Gi6qclW7bd3taWe3jyYGZgfIaecXXIm9JVhr4YxqYXbIyMua1HoUrH9na7LQ3KU8xtjnKtajghOoYewzj5T31EX4tc17edIlwlM7w0ECp2lGQMO7ydSwBRbb2j89hZ6HzsaHYVg4jyGTPs4aIvztcX8F3zHPnaYj8mBg5DxZHvH5OXu9nn6UMye7h-nN7PCSFH2hURVVoYLzSa6tc62jgmYaGWd1pppjpWYcAY116iA2UoKLVqu3LCNKyutGJPzTe8yxY8V5r5Z-GwwBOgwrnKjmeKTUnE5OC82TpNizglds0x-AWndcNb8omz-UQ7ms20t5AGJS9AZn3eJUtQVG9iKH2zbdBI</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>ZOTOVA, Natalia</creator><creator>HELLGARDT, Klaus</creator><creator>KELSALL, Geoffrey H</creator><creator>JESSIMAN, Alan S</creator><creator>HII, King Kuok</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>20100101</creationdate><title>Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones</title><author>ZOTOVA, Natalia ; HELLGARDT, Klaus ; KELSALL, Geoffrey H ; JESSIMAN, Alan S ; HII, King Kuok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-4e725c139089bdfdbf03a897df999091e53810a619e7a0d54393b17f46317d4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Applied sciences</topic><topic>Chemical engineering</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Kinetics and mechanisms</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><topic>Reactors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZOTOVA, Natalia</creatorcontrib><creatorcontrib>HELLGARDT, Klaus</creatorcontrib><creatorcontrib>KELSALL, Geoffrey H</creatorcontrib><creatorcontrib>JESSIMAN, Alan S</creatorcontrib><creatorcontrib>HII, King Kuok</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZOTOVA, Natalia</au><au>HELLGARDT, Klaus</au><au>KELSALL, Geoffrey H</au><au>JESSIMAN, Alan S</au><au>HII, King Kuok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2010-01-01</date><risdate>2010</risdate><volume>12</volume><issue>12</issue><spage>2157</spage><epage>2163</epage><pages>2157-2163</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>A safe, practical and selective process for the aerobic oxidation of alcohols to aldehydes and ketones has been developed using an Ru catalyst in a continuous flow reactor. Benzylic and allylic alcohols are oxidised selectively to their corresponding aldehydes and ketones, including substrates containing N- and S-heteroatoms. The rate of turnover is compatible with that previously reported using batch or microchannel reactors under optimised conditions. A preliminary kinetic model is derived that is supported by experimental observations. Last but not least, tandem oxidation-olefination may be achieved without the need to isolate the alcohol intermediate or to switch solvent.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c0gc00493f</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1463-9262 |
ispartof | Green chemistry : an international journal and green chemistry resource : GC, 2010-01, Vol.12 (12), p.2157-2163 |
issn | 1463-9262 1463-9270 |
language | eng |
recordid | cdi_proquest_miscellaneous_907182714 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Applied sciences Chemical engineering Chemistry Exact sciences and technology Kinetics and mechanisms Organic chemistry Reactivity and mechanisms Reactors |
title | Catalysis in flow: the practical and selective aerobic oxidation of alcohols to aldehydes and ketones |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T05%3A24%3A20IST&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=Catalysis%20in%20flow:%20the%20practical%20and%20selective%20aerobic%20oxidation%20of%20alcohols%20to%20aldehydes%20and%20ketones&rft.jtitle=Green%20chemistry%20:%20an%20international%20journal%20and%20green%20chemistry%20resource%20:%20GC&rft.au=ZOTOVA,%20Natalia&rft.date=2010-01-01&rft.volume=12&rft.issue=12&rft.spage=2157&rft.epage=2163&rft.pages=2157-2163&rft.issn=1463-9262&rft.eissn=1463-9270&rft_id=info:doi/10.1039/c0gc00493f&rft_dat=%3Cproquest_cross%3E907182714%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=907182714&rft_id=info:pmid/&rfr_iscdi=true |