Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus

Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus

Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionali...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic & biomolecular chemistry 2010-10, Vol.8 (2), p.453-4513
Hauptverfasser: Ackermann, Lutz, Potukuchi, Harish Kumar
Format: Artikel
Sprache:eng
Schlagworte:
Alkynes - chemistry
Catalysis
Copper - chemistry
Kinetics
Organometallic Compounds - chemistry
Triazoles - chemical synthesis
Triazoles - chemistry
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4513
container_issue 2
container_start_page 453
container_title Organic & biomolecular chemistry
container_volume 8
creator Ackermann, Lutz
Potukuchi, Harish Kumar
description Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations. This perspective article summarizes progress in this research area until June 2010. Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations.
doi_str_mv 10.1039/c0ob00212g
format Article
fullrecord <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_proquest_miscellaneous_756299679</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>756299679</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-2bfa4491ac3b2c6759e7942f27cba92d4c83ced05ce8f169d7f612e5e5a3fdd63</originalsourceid><addsrcrecordid>eNp9kE1Lw0AURQdRrFY37pW4EqSx85FkOu5KUCsUBNF1mMy8qZE0U_MSsf31prRW3Lh6F-55Z3EJOWP0hlGhhob6nFLO-GyPHLFIypDGQu3vMqc9coz4TilTMokOSY9TKYSS_IgUzzArPEIJpik-IcBl1bwBAgbeBa4ty2WIbY5N0bQN2IAN-ECETV3olS8Bb4MODtJ2PE6HaTgJcl_Z7qvqXL7SZbHS6xBU8NXiCTlwukQ43d4-eb2_e0kn4fTp4TEdT0MTUdqEPHc6ihTTRuTcJDJWIFXEHZcm14rbyIyEAUtjAyPHEmWlSxiHGGItnLWJ6JOrjXdR-48WsMnmBRooS12BbzGTccKVSqTqyOsNaWqPWIPLFnUx1_UyYzRbL5v9LtvBF1ttm8_B7tCfKTvgfAPUaHbtH8Hlf322sE58AzV9ilk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>756299679</pqid></control><display><type>article</type><title>Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus</title><source>MEDLINE</source><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Ackermann, Lutz ; Potukuchi, Harish Kumar</creator><creatorcontrib>Ackermann, Lutz ; Potukuchi, Harish Kumar</creatorcontrib><description>Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations. This perspective article summarizes progress in this research area until June 2010. Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c0ob00212g</identifier><identifier>PMID: 20733972</identifier><language>eng</language><publisher>England</publisher><subject>Alkynes - chemistry ; Catalysis ; Copper - chemistry ; Kinetics ; Organometallic Compounds - chemistry ; Triazoles - chemical synthesis ; Triazoles - chemistry</subject><ispartof>Organic &amp; biomolecular chemistry, 2010-10, Vol.8 (2), p.453-4513</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-2bfa4491ac3b2c6759e7942f27cba92d4c83ced05ce8f169d7f612e5e5a3fdd63</citedby><cites>FETCH-LOGICAL-c400t-2bfa4491ac3b2c6759e7942f27cba92d4c83ced05ce8f169d7f612e5e5a3fdd63</cites></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/20733972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ackermann, Lutz</creatorcontrib><creatorcontrib>Potukuchi, Harish Kumar</creatorcontrib><title>Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus</title><title>Organic &amp; biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations. This perspective article summarizes progress in this research area until June 2010. Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations.</description><subject>Alkynes - chemistry</subject><subject>Catalysis</subject><subject>Copper - chemistry</subject><subject>Kinetics</subject><subject>Organometallic Compounds - chemistry</subject><subject>Triazoles - chemical synthesis</subject><subject>Triazoles - chemistry</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1Lw0AURQdRrFY37pW4EqSx85FkOu5KUCsUBNF1mMy8qZE0U_MSsf31prRW3Lh6F-55Z3EJOWP0hlGhhob6nFLO-GyPHLFIypDGQu3vMqc9coz4TilTMokOSY9TKYSS_IgUzzArPEIJpik-IcBl1bwBAgbeBa4ty2WIbY5N0bQN2IAN-ECETV3olS8Bb4MODtJ2PE6HaTgJcl_Z7qvqXL7SZbHS6xBU8NXiCTlwukQ43d4-eb2_e0kn4fTp4TEdT0MTUdqEPHc6ihTTRuTcJDJWIFXEHZcm14rbyIyEAUtjAyPHEmWlSxiHGGItnLWJ6JOrjXdR-48WsMnmBRooS12BbzGTccKVSqTqyOsNaWqPWIPLFnUx1_UyYzRbL5v9LtvBF1ttm8_B7tCfKTvgfAPUaHbtH8Hlf322sE58AzV9ilk</recordid><startdate>20101021</startdate><enddate>20101021</enddate><creator>Ackermann, Lutz</creator><creator>Potukuchi, Harish Kumar</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20101021</creationdate><title>Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus</title><author>Ackermann, Lutz ; Potukuchi, Harish Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-2bfa4491ac3b2c6759e7942f27cba92d4c83ced05ce8f169d7f612e5e5a3fdd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alkynes - chemistry</topic><topic>Catalysis</topic><topic>Copper - chemistry</topic><topic>Kinetics</topic><topic>Organometallic Compounds - chemistry</topic><topic>Triazoles - chemical synthesis</topic><topic>Triazoles - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ackermann, Lutz</creatorcontrib><creatorcontrib>Potukuchi, Harish Kumar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic &amp; biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ackermann, Lutz</au><au>Potukuchi, Harish Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus</atitle><jtitle>Organic &amp; biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2010-10-21</date><risdate>2010</risdate><volume>8</volume><issue>2</issue><spage>453</spage><epage>4513</epage><pages>453-4513</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations. This perspective article summarizes progress in this research area until June 2010. Regioselective syntheses of 1,4,5-trisubstituted 1,2,3-triazoles were accomplished by three different strategies, relying on (i) the interception of stoichiometrically formed 5-cuprated-1,2,3-triazoles, (ii) the use of stoichiometrically functionalized alkynes or (iii) catalytic C-H bond functionalizations.</abstract><cop>England</cop><pmid>20733972</pmid><doi>10.1039/c0ob00212g</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1477-0520
ispartof Organic & biomolecular chemistry, 2010-10, Vol.8 (2), p.453-4513
issn 1477-0520
1477-0539
language eng
recordid cdi_proquest_miscellaneous_756299679
source MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Alkynes - chemistry
Catalysis
Copper - chemistry
Kinetics
Organometallic Compounds - chemistry
Triazoles - chemical synthesis
Triazoles - chemistry
title Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C-H bond functionalization nexus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T06%3A39%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_rsc_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regioselective%20syntheses%20of%20fully-substituted%201,2,3-triazoles:%20the%20CuAAC/C-H%20bond%20functionalization%20nexus&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=Ackermann,%20Lutz&rft.date=2010-10-21&rft.volume=8&rft.issue=2&rft.spage=453&rft.epage=4513&rft.pages=453-4513&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/c0ob00212g&rft_dat=%3Cproquest_rsc_p%3E756299679%3C/proquest_rsc_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=756299679&rft_id=info:pmid/20733972&rfr_iscdi=true