Sodium Phosphaethynolate as a Building Block for Heterocycles
Phosphorus‐containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a chal...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie International Edition 2014-02, Vol.53 (6), p.1641-1645 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1645 |
---|---|
container_issue | 6 |
container_start_page | 1641 |
container_title | Angewandte Chemie International Edition |
container_volume | 53 |
creator | Chen, Xiaodan Alidori, Simone Puschmann, Florian Frank Santiso-Quinones, Gustavo Benkő, Zoltán Li, Zhongshu Becker, Gerd Grützmacher, Hans-Friedrich Grützmacher, Hansjörg |
description | Phosphorus‐containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we report the use of the phosphaethynolate (OCP)− anion as a building block for various sterically unprotected and functionalized hydroxy substituted phosphorus heterocycles. Because the resulting heterocycles are themselves anions, they are building blocks in their own right and allow further facile functionalization. This property may be of interest in coordination chemistry and material science.
Small, but effective—such is the nature of the OCP− anion of the sodium phosphaethynolate salt. In atom‐economic cycloadditions, several five‐ and six‐membered phosphorus heterocycles are accessed, all of which are useful building blocks in their own right. |
doi_str_mv | 10.1002/anie.201308220 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1700998063</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1499126939</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5470-3f414ca8b30bd79d8d02d11f8bef09696729a9177648d3f5420054bdf8c1e7993</originalsourceid><addsrcrecordid>eNqFkTtP7DAQRi10Ee-WEkW6DU2W8Su2Cwrei0A8BAiJxnJihw1k48VOBPvvyWphhWioZorzHWnmQ2gbwwADkD3TVG5AAFOQhMASWsOc4JQKQf_1O6M0FZLjVbQe40vPSwnZCloljHGKqVpD-3feVt04uRn5OBkZ146mja9N6xITE5McdlVtq-Y5Oax98ZqUPiRD17rgi2lRu7iJlktTR7f1NTfQw-nJ_dEwvbw-Oz86uEwLzgSktGSYFUbmFHIrlJUWiMW4lLkrQWUqE0QZhYXImLS05IwAcJbbUhbYCaXoBtqdeyfBv3UutnpcxcLVtWmc76LGAkCp_jb6N8qUwiRTdGb9_wt98V1o-kNmFAMuMyV6ajCniuBjDK7Uk1CNTZhqDHrWgZ51oBcd9IGdL22Xj51d4N9P7wE1B96r2k3_0OmDq_OTn_J0nq1i6z4WWRNedSao4Prx6kwfDy_E0939reb0EzGjn1g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1494058697</pqid></control><display><type>article</type><title>Sodium Phosphaethynolate as a Building Block for Heterocycles</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Chen, Xiaodan ; Alidori, Simone ; Puschmann, Florian Frank ; Santiso-Quinones, Gustavo ; Benkő, Zoltán ; Li, Zhongshu ; Becker, Gerd ; Grützmacher, Hans-Friedrich ; Grützmacher, Hansjörg</creator><creatorcontrib>Chen, Xiaodan ; Alidori, Simone ; Puschmann, Florian Frank ; Santiso-Quinones, Gustavo ; Benkő, Zoltán ; Li, Zhongshu ; Becker, Gerd ; Grützmacher, Hans-Friedrich ; Grützmacher, Hansjörg</creatorcontrib><description>Phosphorus‐containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we report the use of the phosphaethynolate (OCP)− anion as a building block for various sterically unprotected and functionalized hydroxy substituted phosphorus heterocycles. Because the resulting heterocycles are themselves anions, they are building blocks in their own right and allow further facile functionalization. This property may be of interest in coordination chemistry and material science.
Small, but effective—such is the nature of the OCP− anion of the sodium phosphaethynolate salt. In atom‐economic cycloadditions, several five‐ and six‐membered phosphorus heterocycles are accessed, all of which are useful building blocks in their own right.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201308220</identifier><identifier>PMID: 24453139</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Anions ; Catalysis ; Cycloaddition ; Ligands ; Materials science ; multiple bonds ; phosphinines ; Phosphorus ; phosphorus heterocycles ; Sodium ; sodium phosphaethynolate ; Synthesis</subject><ispartof>Angewandte Chemie International Edition, 2014-02, Vol.53 (6), p.1641-1645</ispartof><rights>Copyright © 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5470-3f414ca8b30bd79d8d02d11f8bef09696729a9177648d3f5420054bdf8c1e7993</citedby><cites>FETCH-LOGICAL-c5470-3f414ca8b30bd79d8d02d11f8bef09696729a9177648d3f5420054bdf8c1e7993</cites></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.201308220$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.201308220$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24453139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Xiaodan</creatorcontrib><creatorcontrib>Alidori, Simone</creatorcontrib><creatorcontrib>Puschmann, Florian Frank</creatorcontrib><creatorcontrib>Santiso-Quinones, Gustavo</creatorcontrib><creatorcontrib>Benkő, Zoltán</creatorcontrib><creatorcontrib>Li, Zhongshu</creatorcontrib><creatorcontrib>Becker, Gerd</creatorcontrib><creatorcontrib>Grützmacher, Hans-Friedrich</creatorcontrib><creatorcontrib>Grützmacher, Hansjörg</creatorcontrib><title>Sodium Phosphaethynolate as a Building Block for Heterocycles</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>Phosphorus‐containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we report the use of the phosphaethynolate (OCP)− anion as a building block for various sterically unprotected and functionalized hydroxy substituted phosphorus heterocycles. Because the resulting heterocycles are themselves anions, they are building blocks in their own right and allow further facile functionalization. This property may be of interest in coordination chemistry and material science.
Small, but effective—such is the nature of the OCP− anion of the sodium phosphaethynolate salt. In atom‐economic cycloadditions, several five‐ and six‐membered phosphorus heterocycles are accessed, all of which are useful building blocks in their own right.</description><subject>Anions</subject><subject>Catalysis</subject><subject>Cycloaddition</subject><subject>Ligands</subject><subject>Materials science</subject><subject>multiple bonds</subject><subject>phosphinines</subject><subject>Phosphorus</subject><subject>phosphorus heterocycles</subject><subject>Sodium</subject><subject>sodium phosphaethynolate</subject><subject>Synthesis</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkTtP7DAQRi10Ee-WEkW6DU2W8Su2Cwrei0A8BAiJxnJihw1k48VOBPvvyWphhWioZorzHWnmQ2gbwwADkD3TVG5AAFOQhMASWsOc4JQKQf_1O6M0FZLjVbQe40vPSwnZCloljHGKqVpD-3feVt04uRn5OBkZ146mja9N6xITE5McdlVtq-Y5Oax98ZqUPiRD17rgi2lRu7iJlktTR7f1NTfQw-nJ_dEwvbw-Oz86uEwLzgSktGSYFUbmFHIrlJUWiMW4lLkrQWUqE0QZhYXImLS05IwAcJbbUhbYCaXoBtqdeyfBv3UutnpcxcLVtWmc76LGAkCp_jb6N8qUwiRTdGb9_wt98V1o-kNmFAMuMyV6ajCniuBjDK7Uk1CNTZhqDHrWgZ51oBcd9IGdL22Xj51d4N9P7wE1B96r2k3_0OmDq_OTn_J0nq1i6z4WWRNedSao4Prx6kwfDy_E0939reb0EzGjn1g</recordid><startdate>20140203</startdate><enddate>20140203</enddate><creator>Chen, Xiaodan</creator><creator>Alidori, Simone</creator><creator>Puschmann, Florian Frank</creator><creator>Santiso-Quinones, Gustavo</creator><creator>Benkő, Zoltán</creator><creator>Li, Zhongshu</creator><creator>Becker, Gerd</creator><creator>Grützmacher, Hans-Friedrich</creator><creator>Grützmacher, Hansjörg</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20140203</creationdate><title>Sodium Phosphaethynolate as a Building Block for Heterocycles</title><author>Chen, Xiaodan ; Alidori, Simone ; Puschmann, Florian Frank ; Santiso-Quinones, Gustavo ; Benkő, Zoltán ; Li, Zhongshu ; Becker, Gerd ; Grützmacher, Hans-Friedrich ; Grützmacher, Hansjörg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5470-3f414ca8b30bd79d8d02d11f8bef09696729a9177648d3f5420054bdf8c1e7993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anions</topic><topic>Catalysis</topic><topic>Cycloaddition</topic><topic>Ligands</topic><topic>Materials science</topic><topic>multiple bonds</topic><topic>phosphinines</topic><topic>Phosphorus</topic><topic>phosphorus heterocycles</topic><topic>Sodium</topic><topic>sodium phosphaethynolate</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Xiaodan</creatorcontrib><creatorcontrib>Alidori, Simone</creatorcontrib><creatorcontrib>Puschmann, Florian Frank</creatorcontrib><creatorcontrib>Santiso-Quinones, Gustavo</creatorcontrib><creatorcontrib>Benkő, Zoltán</creatorcontrib><creatorcontrib>Li, Zhongshu</creatorcontrib><creatorcontrib>Becker, Gerd</creatorcontrib><creatorcontrib>Grützmacher, Hans-Friedrich</creatorcontrib><creatorcontrib>Grützmacher, Hansjörg</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Xiaodan</au><au>Alidori, Simone</au><au>Puschmann, Florian Frank</au><au>Santiso-Quinones, Gustavo</au><au>Benkő, Zoltán</au><au>Li, Zhongshu</au><au>Becker, Gerd</au><au>Grützmacher, Hans-Friedrich</au><au>Grützmacher, Hansjörg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sodium Phosphaethynolate as a Building Block for Heterocycles</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2014-02-03</date><risdate>2014</risdate><volume>53</volume><issue>6</issue><spage>1641</spage><epage>1645</epage><pages>1641-1645</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Phosphorus‐containing heterocycles have evolved from laboratory curiosities to functional components, such as ligands in catalytically active metal complexes or molecular constituents in electronic devices. The straightforward synthesis of functionalized heterocycles on a larger scale remains a challenge. Herein, we report the use of the phosphaethynolate (OCP)− anion as a building block for various sterically unprotected and functionalized hydroxy substituted phosphorus heterocycles. Because the resulting heterocycles are themselves anions, they are building blocks in their own right and allow further facile functionalization. This property may be of interest in coordination chemistry and material science.
Small, but effective—such is the nature of the OCP− anion of the sodium phosphaethynolate salt. In atom‐economic cycloadditions, several five‐ and six‐membered phosphorus heterocycles are accessed, all of which are useful building blocks in their own right.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>24453139</pmid><doi>10.1002/anie.201308220</doi><tpages>5</tpages><edition>International ed. in English</edition></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2014-02, Vol.53 (6), p.1641-1645 |
issn | 1433-7851 1521-3773 |
language | eng |
recordid | cdi_proquest_miscellaneous_1700998063 |
source | Wiley Online Library Journals Frontfile Complete |
subjects | Anions Catalysis Cycloaddition Ligands Materials science multiple bonds phosphinines Phosphorus phosphorus heterocycles Sodium sodium phosphaethynolate Synthesis |
title | Sodium Phosphaethynolate as a Building Block for Heterocycles |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T00%3A29%3A47IST&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=Sodium%20Phosphaethynolate%20as%20a%20Building%20Block%20for%20Heterocycles&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Chen,%20Xiaodan&rft.date=2014-02-03&rft.volume=53&rft.issue=6&rft.spage=1641&rft.epage=1645&rft.pages=1641-1645&rft.issn=1433-7851&rft.eissn=1521-3773&rft.coden=ACIEAY&rft_id=info:doi/10.1002/anie.201308220&rft_dat=%3Cproquest_cross%3E1499126939%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=1494058697&rft_id=info:pmid/24453139&rfr_iscdi=true |