Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis

A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported. Employing the well‐defined Mn‐MACHOPh as the catalyst, this novel protocol has a broad substrate scope with good functional grou...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie International Edition 2023-06, Vol.62 (26), p.e202303433-n/a
Hauptverfasser: Sun, Feixiang, Huang, Jiamin, Wei, Zhihong, Tang, Conghui, Liu, Weiping
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 26
container_start_page e202303433
container_title Angewandte Chemie International Edition
container_volume 62
creator Sun, Feixiang
Huang, Jiamin
Wei, Zhihong
Tang, Conghui
Liu, Weiping
description A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported. Employing the well‐defined Mn‐MACHOPh as the catalyst, this novel protocol has a broad substrate scope with good functional group tolerance and affords a diverse library of valuable disubstituted alcohols and ketones in moderate to good yields. The strong influence of the reaction temperature on the selective formation of alcohol products was theorized in preliminary DFT studies. Studies have shown that the Gibbs free energy of the formation of alcohols is thermodynamically more favourable than corresponding ketones at a lower temperature. A manganese‐catalyzed cross‐coupling of two secondary alcohols in a divergent synthesis of either γ‐disubstituted alcohols or β‐disubstituted ketones is herein reported. A wide range of different alcohols could undergo the cross‐coupling process smoothly and furnish the corresponding products by using the same catalyst, with overall moderate to good yields.
doi_str_mv 10.1002/anie.202303433
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2805030651</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2805030651</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3733-8cd93e752bdce94370c1de281b145c13337ced3fd3c97fe8048e530da485834c3</originalsourceid><addsrcrecordid>eNqFkUFPGzEQha0KVFLaK0dkiQuXBNuzXjvHaKGACO2B9rxy7Nmw0cYO611Qbv0J_Mb-EhwFgsSF01ij7z09zyPkiLMRZ0ycGV_jSDABDDKAL2TApeBDUAr20juthkpLfkC-xbhIvNYs_0oOQDENTOQDsjqvH7Gdo-_o3dp39xjrSENFJ40N96GJ1HhHb7ALHiN9rA0t2hDj_3_PRehXTe3nG_gObfDOtOt3We8dtvTW-LlJSqSF6UyzTubfyX5lmog_Xuch-fvz4k9xNZz-vrwuJtOhBZVSa-vGgEqKmbM4zlJgyx0KzWc8k5YDgLLooHJgx6pCzTKNEpgzmZYaMguH5HTru2rDQ4-xK5d1tNg0KU_oYyk0kwxYLnlCTz6gi9C3PqVLlMglZDJXiRptKbu5QItVuWrrZfp0yVm56aLcdFHuukiC41fbfrZEt8Pfjp-A8RZ4qhtcf2JXTn5dX7ybvwBQX5bP</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2826534567</pqid></control><display><type>article</type><title>Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Sun, Feixiang ; Huang, Jiamin ; Wei, Zhihong ; Tang, Conghui ; Liu, Weiping</creator><creatorcontrib>Sun, Feixiang ; Huang, Jiamin ; Wei, Zhihong ; Tang, Conghui ; Liu, Weiping</creatorcontrib><description>A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported. Employing the well‐defined Mn‐MACHOPh as the catalyst, this novel protocol has a broad substrate scope with good functional group tolerance and affords a diverse library of valuable disubstituted alcohols and ketones in moderate to good yields. The strong influence of the reaction temperature on the selective formation of alcohol products was theorized in preliminary DFT studies. Studies have shown that the Gibbs free energy of the formation of alcohols is thermodynamically more favourable than corresponding ketones at a lower temperature. A manganese‐catalyzed cross‐coupling of two secondary alcohols in a divergent synthesis of either γ‐disubstituted alcohols or β‐disubstituted ketones is herein reported. A wide range of different alcohols could undergo the cross‐coupling process smoothly and furnish the corresponding products by using the same catalyst, with overall moderate to good yields.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202303433</identifier><identifier>PMID: 37083026</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alcohols ; Borrowing Hydrogen ; Catalysis ; Catalysts ; Cross coupling ; Divergence ; Free energy ; Functional groups ; Gibbs free energy ; Homogeneous Catalysis ; Ketones ; Low temperature ; Manganese ; Molecular Structure ; Oxidation-Reduction ; Substrates ; Synthesis</subject><ispartof>Angewandte Chemie International Edition, 2023-06, Vol.62 (26), p.e202303433-n/a</ispartof><rights>2023 Wiley‐VCH GmbH</rights><rights>2023 Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3733-8cd93e752bdce94370c1de281b145c13337ced3fd3c97fe8048e530da485834c3</citedby><cites>FETCH-LOGICAL-c3733-8cd93e752bdce94370c1de281b145c13337ced3fd3c97fe8048e530da485834c3</cites><orcidid>0000-0002-1064-7276</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202303433$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202303433$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37083026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Feixiang</creatorcontrib><creatorcontrib>Huang, Jiamin</creatorcontrib><creatorcontrib>Wei, Zhihong</creatorcontrib><creatorcontrib>Tang, Conghui</creatorcontrib><creatorcontrib>Liu, Weiping</creatorcontrib><title>Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported. Employing the well‐defined Mn‐MACHOPh as the catalyst, this novel protocol has a broad substrate scope with good functional group tolerance and affords a diverse library of valuable disubstituted alcohols and ketones in moderate to good yields. The strong influence of the reaction temperature on the selective formation of alcohol products was theorized in preliminary DFT studies. Studies have shown that the Gibbs free energy of the formation of alcohols is thermodynamically more favourable than corresponding ketones at a lower temperature. A manganese‐catalyzed cross‐coupling of two secondary alcohols in a divergent synthesis of either γ‐disubstituted alcohols or β‐disubstituted ketones is herein reported. A wide range of different alcohols could undergo the cross‐coupling process smoothly and furnish the corresponding products by using the same catalyst, with overall moderate to good yields.</description><subject>Alcohols</subject><subject>Borrowing Hydrogen</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Cross coupling</subject><subject>Divergence</subject><subject>Free energy</subject><subject>Functional groups</subject><subject>Gibbs free energy</subject><subject>Homogeneous Catalysis</subject><subject>Ketones</subject><subject>Low temperature</subject><subject>Manganese</subject><subject>Molecular Structure</subject><subject>Oxidation-Reduction</subject><subject>Substrates</subject><subject>Synthesis</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkUFPGzEQha0KVFLaK0dkiQuXBNuzXjvHaKGACO2B9rxy7Nmw0cYO611Qbv0J_Mb-EhwFgsSF01ij7z09zyPkiLMRZ0ycGV_jSDABDDKAL2TApeBDUAr20juthkpLfkC-xbhIvNYs_0oOQDENTOQDsjqvH7Gdo-_o3dp39xjrSENFJ40N96GJ1HhHb7ALHiN9rA0t2hDj_3_PRehXTe3nG_gObfDOtOt3We8dtvTW-LlJSqSF6UyzTubfyX5lmog_Xuch-fvz4k9xNZz-vrwuJtOhBZVSa-vGgEqKmbM4zlJgyx0KzWc8k5YDgLLooHJgx6pCzTKNEpgzmZYaMguH5HTru2rDQ4-xK5d1tNg0KU_oYyk0kwxYLnlCTz6gi9C3PqVLlMglZDJXiRptKbu5QItVuWrrZfp0yVm56aLcdFHuukiC41fbfrZEt8Pfjp-A8RZ4qhtcf2JXTn5dX7ybvwBQX5bP</recordid><startdate>20230626</startdate><enddate>20230626</enddate><creator>Sun, Feixiang</creator><creator>Huang, Jiamin</creator><creator>Wei, Zhihong</creator><creator>Tang, Conghui</creator><creator>Liu, Weiping</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1064-7276</orcidid></search><sort><creationdate>20230626</creationdate><title>Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis</title><author>Sun, Feixiang ; Huang, Jiamin ; Wei, Zhihong ; Tang, Conghui ; Liu, Weiping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3733-8cd93e752bdce94370c1de281b145c13337ced3fd3c97fe8048e530da485834c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alcohols</topic><topic>Borrowing Hydrogen</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Cross coupling</topic><topic>Divergence</topic><topic>Free energy</topic><topic>Functional groups</topic><topic>Gibbs free energy</topic><topic>Homogeneous Catalysis</topic><topic>Ketones</topic><topic>Low temperature</topic><topic>Manganese</topic><topic>Molecular Structure</topic><topic>Oxidation-Reduction</topic><topic>Substrates</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Feixiang</creatorcontrib><creatorcontrib>Huang, Jiamin</creatorcontrib><creatorcontrib>Wei, Zhihong</creatorcontrib><creatorcontrib>Tang, Conghui</creatorcontrib><creatorcontrib>Liu, Weiping</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Feixiang</au><au>Huang, Jiamin</au><au>Wei, Zhihong</au><au>Tang, Conghui</au><au>Liu, Weiping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2023-06-26</date><risdate>2023</risdate><volume>62</volume><issue>26</issue><spage>e202303433</spage><epage>n/a</epage><pages>e202303433-n/a</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported. Employing the well‐defined Mn‐MACHOPh as the catalyst, this novel protocol has a broad substrate scope with good functional group tolerance and affords a diverse library of valuable disubstituted alcohols and ketones in moderate to good yields. The strong influence of the reaction temperature on the selective formation of alcohol products was theorized in preliminary DFT studies. Studies have shown that the Gibbs free energy of the formation of alcohols is thermodynamically more favourable than corresponding ketones at a lower temperature. A manganese‐catalyzed cross‐coupling of two secondary alcohols in a divergent synthesis of either γ‐disubstituted alcohols or β‐disubstituted ketones is herein reported. A wide range of different alcohols could undergo the cross‐coupling process smoothly and furnish the corresponding products by using the same catalyst, with overall moderate to good yields.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37083026</pmid><doi>10.1002/anie.202303433</doi><tpages>8</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-1064-7276</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2023-06, Vol.62 (26), p.e202303433-n/a
issn 1433-7851
1521-3773
language eng
recordid cdi_proquest_miscellaneous_2805030651
source Wiley Online Library Journals Frontfile Complete
subjects Alcohols
Borrowing Hydrogen
Catalysis
Catalysts
Cross coupling
Divergence
Free energy
Functional groups
Gibbs free energy
Homogeneous Catalysis
Ketones
Low temperature
Manganese
Molecular Structure
Oxidation-Reduction
Substrates
Synthesis
title Divergent Synthesis of Alcohols and Ketones via Cross‐Coupling of Secondary Alcohols under Manganese Catalysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T23%3A33%3A32IST&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=Divergent%20Synthesis%20of%20Alcohols%20and%20Ketones%20via%20Cross%E2%80%90Coupling%20of%20Secondary%20Alcohols%20under%20Manganese%20Catalysis&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Sun,%20Feixiang&rft.date=2023-06-26&rft.volume=62&rft.issue=26&rft.spage=e202303433&rft.epage=n/a&rft.pages=e202303433-n/a&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202303433&rft_dat=%3Cproquest_cross%3E2805030651%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=2826534567&rft_id=info:pmid/37083026&rfr_iscdi=true