D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes
From a single alkene to two different alkenes! An iron-catalyzed four-component reaction involving an aldehyde, two different alkenes and TMSN 3 is developed to assemble these four reactants in an orderly fashion based on the inherent nucleophilic/electrophilic reaction activity of the radicals and...
Gespeichert in:
| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2023-06, Vol.59 (51), p.7986-7989 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 7989 |
|---|---|
| container_issue | 51 |
| container_start_page | 7986 |
| container_title | Chemical communications (Cambridge, England) |
| container_volume | 59 |
| creator | Liu, Ren-Xiang Chen, Xin Yang, Luo |
| description | From a single alkene to two different alkenes! An iron-catalyzed four-component reaction involving an aldehyde, two different alkenes and TMSN
3
is developed to assemble these four reactants in an orderly fashion based on the inherent nucleophilic/electrophilic reaction activity of the radicals and alkenes
via
a double radical addition, providing various multifunctional compounds containing an azido group and two carbonyl groups.
From a single alkene to two different alkenes! An iron-catalyzed four-component reaction of aldehydes, two different alkenes and TMSN
3
is developed to orderly assemble these four reactants according to their inherent nucleo/electrophilic activity. |
| doi_str_mv | 10.1039/d3cc01463k |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2823498702</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2828340842</sourcerecordid><originalsourceid>FETCH-LOGICAL-c337t-1b6277f4db3d9a1f8bf6bab41e80aa55b7ec9ddfd37d87eb9b827c481762a2813</originalsourceid><addsrcrecordid>eNpdkUtLxDAUhYMovjfulYIbEaJNkzbpcpjxhYKbEdyVmxd0pm3GpFXGX287M45gNvfm5rsHcg5CZyS-ITHNbzVVKiYso_MddEhoxnDKxPvu0Kc55pSlB-gohFncH5KKfXRAeSIYF_wQ1RM8whM8xe1yYSLrOo-VqxeuMU0bedClgirSHVRYl7ZrVFu6BqryG4YmgkZHoJZVf_s0EXyXej13Nmq_XNSvWOMHJajmpjHhBO1ZqII53dRj9HZ_Nx0_4pfXh6fx6AUrSnmLicwSzi3TkuociBXSZhIkI0bEAGkquVG51lZTrgU3Mpci4YoJwrMEEkHoMbpa6y68--hMaIu6DMpUFTTGdaFIREJZLnic9OjlP3TWm9D_cUUJymLBBup6TSnvQvDGFgtf1uCXBYmLIYRiQsfjVQjPPXyxkexkbfQW_XW9B87XgA9q-_qXIv0BVQ2Mzg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2828340842</pqid></control><display><type>article</type><title>D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Liu, Ren-Xiang ; Chen, Xin ; Yang, Luo</creator><creatorcontrib>Liu, Ren-Xiang ; Chen, Xin ; Yang, Luo</creatorcontrib><description>From a single alkene to two different alkenes! An iron-catalyzed four-component reaction involving an aldehyde, two different alkenes and TMSN
3
is developed to assemble these four reactants in an orderly fashion based on the inherent nucleophilic/electrophilic reaction activity of the radicals and alkenes
via
a double radical addition, providing various multifunctional compounds containing an azido group and two carbonyl groups.
From a single alkene to two different alkenes! An iron-catalyzed four-component reaction of aldehydes, two different alkenes and TMSN
3
is developed to orderly assemble these four reactants according to their inherent nucleo/electrophilic activity.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d3cc01463k</identifier><identifier>PMID: 37284787</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Aldehydes ; Alkenes ; Carbonyl groups ; Carbonyls</subject><ispartof>Chemical communications (Cambridge, England), 2023-06, Vol.59 (51), p.7986-7989</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-1b6277f4db3d9a1f8bf6bab41e80aa55b7ec9ddfd37d87eb9b827c481762a2813</citedby><cites>FETCH-LOGICAL-c337t-1b6277f4db3d9a1f8bf6bab41e80aa55b7ec9ddfd37d87eb9b827c481762a2813</cites><orcidid>0000-0002-0061-0816</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37284787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Ren-Xiang</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Yang, Luo</creatorcontrib><title>D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>From a single alkene to two different alkenes! An iron-catalyzed four-component reaction involving an aldehyde, two different alkenes and TMSN
3
is developed to assemble these four reactants in an orderly fashion based on the inherent nucleophilic/electrophilic reaction activity of the radicals and alkenes
via
a double radical addition, providing various multifunctional compounds containing an azido group and two carbonyl groups.
From a single alkene to two different alkenes! An iron-catalyzed four-component reaction of aldehydes, two different alkenes and TMSN
3
is developed to orderly assemble these four reactants according to their inherent nucleo/electrophilic activity.</description><subject>Aldehydes</subject><subject>Alkenes</subject><subject>Carbonyl groups</subject><subject>Carbonyls</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLxDAUhYMovjfulYIbEaJNkzbpcpjxhYKbEdyVmxd0pm3GpFXGX287M45gNvfm5rsHcg5CZyS-ITHNbzVVKiYso_MddEhoxnDKxPvu0Kc55pSlB-gohFncH5KKfXRAeSIYF_wQ1RM8whM8xe1yYSLrOo-VqxeuMU0bedClgirSHVRYl7ZrVFu6BqryG4YmgkZHoJZVf_s0EXyXej13Nmq_XNSvWOMHJajmpjHhBO1ZqII53dRj9HZ_Nx0_4pfXh6fx6AUrSnmLicwSzi3TkuociBXSZhIkI0bEAGkquVG51lZTrgU3Mpci4YoJwrMEEkHoMbpa6y68--hMaIu6DMpUFTTGdaFIREJZLnic9OjlP3TWm9D_cUUJymLBBup6TSnvQvDGFgtf1uCXBYmLIYRiQsfjVQjPPXyxkexkbfQW_XW9B87XgA9q-_qXIv0BVQ2Mzg</recordid><startdate>20230622</startdate><enddate>20230622</enddate><creator>Liu, Ren-Xiang</creator><creator>Chen, Xin</creator><creator>Yang, Luo</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0061-0816</orcidid></search><sort><creationdate>20230622</creationdate><title>D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes</title><author>Liu, Ren-Xiang ; Chen, Xin ; Yang, Luo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-1b6277f4db3d9a1f8bf6bab41e80aa55b7ec9ddfd37d87eb9b827c481762a2813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aldehydes</topic><topic>Alkenes</topic><topic>Carbonyl groups</topic><topic>Carbonyls</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Ren-Xiang</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Yang, Luo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Ren-Xiang</au><au>Chen, Xin</au><au>Yang, Luo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2023-06-22</date><risdate>2023</risdate><volume>59</volume><issue>51</issue><spage>7986</spage><epage>7989</epage><pages>7986-7989</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>From a single alkene to two different alkenes! An iron-catalyzed four-component reaction involving an aldehyde, two different alkenes and TMSN
3
is developed to assemble these four reactants in an orderly fashion based on the inherent nucleophilic/electrophilic reaction activity of the radicals and alkenes
via
a double radical addition, providing various multifunctional compounds containing an azido group and two carbonyl groups.
From a single alkene to two different alkenes! An iron-catalyzed four-component reaction of aldehydes, two different alkenes and TMSN
3
is developed to orderly assemble these four reactants according to their inherent nucleo/electrophilic activity.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>37284787</pmid><doi>10.1039/d3cc01463k</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-0061-0816</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2023-06, Vol.59 (51), p.7986-7989 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2823498702 |
| source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
| subjects | Aldehydes Alkenes Carbonyl groups Carbonyls |
| title | D-A-D-T-type four-component radical dual-difunctionalization and acylative azidation of two different alkenes |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T15%3A34%3A48IST&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=D-A-D-T-type%20four-component%20radical%20dual-difunctionalization%20and%20acylative%20azidation%20of%20two%20different%20alkenes&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Liu,%20Ren-Xiang&rft.date=2023-06-22&rft.volume=59&rft.issue=51&rft.spage=7986&rft.epage=7989&rft.pages=7986-7989&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/d3cc01463k&rft_dat=%3Cproquest_cross%3E2828340842%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=2828340842&rft_id=info:pmid/37284787&rfr_iscdi=true |