ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules

ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules

Novel triazolyl derived N1‐sulfonylpyrimidines are obtained through Cu(I)‐catalyzed alkyne‐azide cycloaddition, followed by sulfonylation of the formed triazolyl derivatives under basic conditions.

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemInform 2016-03, Vol.47 (16), p.no-no
Hauptverfasser: Saftic, Dijana, Vianello, Robert, Zinic, Biserka
Format: Artikel
Sprache:eng
Schlagworte:
cycloaddition reactions
pyrimidine derivatives
sulfonamides (hydrazides, ureides) (benzene compounds)
sulfuration, sulfonation, S‐alkylation
triazole derivatives
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page no
container_issue 16
container_start_page no
container_title ChemInform
container_volume 47
creator Saftic, Dijana
Vianello, Robert
Zinic, Biserka
description Novel triazolyl derived N1‐sulfonylpyrimidines are obtained through Cu(I)‐catalyzed alkyne‐azide cycloaddition, followed by sulfonylation of the formed triazolyl derivatives under basic conditions.
doi_str_mv 10.1002/chin.201616099
format Article
fullrecord <record><control><sourceid>proquest_wiley</sourceid><recordid>TN_cdi_proquest_journals_1776705219</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4003863321</sourcerecordid><originalsourceid>FETCH-LOGICAL-p789-4a64e134a457daa98821b29e5c283a0fbe02ba4b95b2086ea16af0fc1b8701273</originalsourceid><addsrcrecordid>eNpNUUtOwzAQtRBIlM-WtSXWAdv5OGZXlV-lAhKUdeSkY2qUOsV2isKKI3AWDsIhOAluCxWr0cy8n_QQOqLkhBLCTqupNieM0IxmRIgt1KMpYxHLMr6NekTENOKp4Ltoz7nngI95znroazCF2dCoxs5wv3Teysqf4fT7_WNstXxr6q5uw03XDkszweMpaItvafg_tLVqTFfjc7B6Ib1egDvDQ-Otfmq1ecL3ELT0QvsOn2ulwIKpwGFtsJ8CXtMDrTG4UfjXDVbanyv5kEb71sNk5fx3fzTu3-dxlQ3fBGbV1uAO0I6StYPD37mPxpcX48F1NLq7Gg76o2jOcxElMkuAxolMUj6RUuQ5oyUTkFYsjyVRJRBWyqQUaclInoGkmVREVbTMOaGMx_voeC07t81LC84Xz01rTXAsKOcZJymjIqDEGvWqa-iKudUzabuCkmLZV7Hsq9j0VQyuh7ebLf4BbSyWqg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1776705219</pqid></control><display><type>article</type><title>ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules</title><source>Wiley Online Library - AutoHoldings Journals</source><creator>Saftic, Dijana ; Vianello, Robert ; Zinic, Biserka</creator><creatorcontrib>Saftic, Dijana ; Vianello, Robert ; Zinic, Biserka</creatorcontrib><description>Novel triazolyl derived N1‐sulfonylpyrimidines are obtained through Cu(I)‐catalyzed alkyne‐azide cycloaddition, followed by sulfonylation of the formed triazolyl derivatives under basic conditions.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201616099</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag</publisher><subject>cycloaddition reactions ; pyrimidine derivatives ; sulfonamides (hydrazides, ureides) (benzene compounds) ; sulfuration, sulfonation, S‐alkylation ; triazole derivatives</subject><ispartof>ChemInform, 2016-03, Vol.47 (16), p.no-no</ispartof><rights>2016 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><rights>2016 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchin.201616099$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.201616099$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids></links><search><creatorcontrib>Saftic, Dijana</creatorcontrib><creatorcontrib>Vianello, Robert</creatorcontrib><creatorcontrib>Zinic, Biserka</creatorcontrib><title>ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules</title><title>ChemInform</title><description>Novel triazolyl derived N1‐sulfonylpyrimidines are obtained through Cu(I)‐catalyzed alkyne‐azide cycloaddition, followed by sulfonylation of the formed triazolyl derivatives under basic conditions.</description><subject>cycloaddition reactions</subject><subject>pyrimidine derivatives</subject><subject>sulfonamides (hydrazides, ureides) (benzene compounds)</subject><subject>sulfuration, sulfonation, S‐alkylation</subject><subject>triazole derivatives</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpNUUtOwzAQtRBIlM-WtSXWAdv5OGZXlV-lAhKUdeSkY2qUOsV2isKKI3AWDsIhOAluCxWr0cy8n_QQOqLkhBLCTqupNieM0IxmRIgt1KMpYxHLMr6NekTENOKp4Ltoz7nngI95znroazCF2dCoxs5wv3Teysqf4fT7_WNstXxr6q5uw03XDkszweMpaItvafg_tLVqTFfjc7B6Ib1egDvDQ-Otfmq1ecL3ELT0QvsOn2ulwIKpwGFtsJ8CXtMDrTG4UfjXDVbanyv5kEb71sNk5fx3fzTu3-dxlQ3fBGbV1uAO0I6StYPD37mPxpcX48F1NLq7Gg76o2jOcxElMkuAxolMUj6RUuQ5oyUTkFYsjyVRJRBWyqQUaclInoGkmVREVbTMOaGMx_voeC07t81LC84Xz01rTXAsKOcZJymjIqDEGvWqa-iKudUzabuCkmLZV7Hsq9j0VQyuh7ebLf4BbSyWqg</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Saftic, Dijana</creator><creator>Vianello, Robert</creator><creator>Zinic, Biserka</creator><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope/></search><sort><creationdate>201603</creationdate><title>ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules</title><author>Saftic, Dijana ; Vianello, Robert ; Zinic, Biserka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p789-4a64e134a457daa98821b29e5c283a0fbe02ba4b95b2086ea16af0fc1b8701273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>cycloaddition reactions</topic><topic>pyrimidine derivatives</topic><topic>sulfonamides (hydrazides, ureides) (benzene compounds)</topic><topic>sulfuration, sulfonation, S‐alkylation</topic><topic>triazole derivatives</topic><toplevel>online_resources</toplevel><creatorcontrib>Saftic, Dijana</creatorcontrib><creatorcontrib>Vianello, Robert</creatorcontrib><creatorcontrib>Zinic, Biserka</creatorcontrib><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saftic, Dijana</au><au>Vianello, Robert</au><au>Zinic, Biserka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules</atitle><jtitle>ChemInform</jtitle><date>2016-03</date><risdate>2016</risdate><volume>47</volume><issue>16</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>Novel triazolyl derived N1‐sulfonylpyrimidines are obtained through Cu(I)‐catalyzed alkyne‐azide cycloaddition, followed by sulfonylation of the formed triazolyl derivatives under basic conditions.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag</pub><doi>10.1002/chin.201616099</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0931-7597
ispartof ChemInform, 2016-03, Vol.47 (16), p.no-no
issn 0931-7597
1522-2667
language eng
recordid cdi_proquest_journals_1776705219
source Wiley Online Library - AutoHoldings Journals
subjects cycloaddition reactions
pyrimidine derivatives
sulfonamides (hydrazides, ureides) (benzene compounds)
sulfuration, sulfonation, S‐alkylation
triazole derivatives
title ChemInform Abstract: 5‐Triazolyluracils and Their N1‐Sulfonyl Derivatives: Intriguing Reactivity Differences in the Sulfonation of Triazole N1′‐Substituted and N1′‐Unsubstituted Uracil Molecules
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T07%3A00%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_wiley&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChemInform%20Abstract:%205%E2%80%90Triazolyluracils%20and%20Their%20N1%E2%80%90Sulfonyl%20Derivatives:%20Intriguing%20Reactivity%20Differences%20in%20the%20Sulfonation%20of%20Triazole%20N1%E2%80%B2%E2%80%90Substituted%20and%20N1%E2%80%B2%E2%80%90Unsubstituted%20Uracil%20Molecules&rft.jtitle=ChemInform&rft.au=Saftic,%20Dijana&rft.date=2016-03&rft.volume=47&rft.issue=16&rft.spage=no&rft.epage=no&rft.pages=no-no&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.201616099&rft_dat=%3Cproquest_wiley%3E4003863321%3C/proquest_wiley%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1776705219&rft_id=info:pmid/&rfr_iscdi=true