A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine

The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions. The selective synthesis of [26]hexaphyri...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Tetrahedron letters 2014-01, Vol.55 (2), p.544-547
Hauptverfasser: Cinar, Seda, Temelli, Baris, Unaleroglu, Canan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 547
container_issue 2
container_start_page 544
container_title Tetrahedron letters
container_volume 55
creator Cinar, Seda
Temelli, Baris
Unaleroglu, Canan
description The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions. The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions.
doi_str_mv 10.1016/j.tetlet.2013.11.101
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1744705744</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0040403913020583</els_id><sourcerecordid>1744705744</sourcerecordid><originalsourceid>FETCH-LOGICAL-c339t-db0c7a16bbb85d88d7e777a8be0021f2ae5652f8aba903daf16649ce24dfc3dd3</originalsourceid><addsrcrecordid>eNp9UMFKxDAUDKLguvoHHnL00po0bZN6EJbFVWHRi55EQpq8uFm67Zpk1f69LfXsO7yBYWZgBqFLSlJKaHm9TSPEBmKaEcpSSkf2CM2o4CxhhaDHaEZITpKcsOoUnYWwJcOVgszQaoFb-MYe1Ae0EdvO47gBHPp2gOAC7ix-y8r3Dfyo_ab3rr3BT0k4NLZr-warxrida-EcnVjVBLj4wzl6Xd29LB-S9fP943KxTjRjVUxMTTRXtKzrWhRGCMOBc65EDYRk1GYKirLIrFC1qggzytKyzCsNWW6sZsawObqacve--zxAiHLngoamUS10hyApz3NOiuEP0nySat-F4MHKvXc75XtJiRxnk1s5zSbH2SSlIzvYbicbDDW-HHgZtINWg3EedJSmc_8H_AJDDXiF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1744705744</pqid></control><display><type>article</type><title>A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Cinar, Seda ; Temelli, Baris ; Unaleroglu, Canan</creator><creatorcontrib>Cinar, Seda ; Temelli, Baris ; Unaleroglu, Canan</creatorcontrib><description>The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions. The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2013.11.101</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Catalysis ; Catalysts ; Expanded porphyrin ; Hexaphyrin ; N-sulfonyl aldimine ; Synthesis (chemistry) ; Tetrahedrons ; Tripyrrane</subject><ispartof>Tetrahedron letters, 2014-01, Vol.55 (2), p.544-547</ispartof><rights>2013 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-db0c7a16bbb85d88d7e777a8be0021f2ae5652f8aba903daf16649ce24dfc3dd3</citedby><cites>FETCH-LOGICAL-c339t-db0c7a16bbb85d88d7e777a8be0021f2ae5652f8aba903daf16649ce24dfc3dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tetlet.2013.11.101$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids></links><search><creatorcontrib>Cinar, Seda</creatorcontrib><creatorcontrib>Temelli, Baris</creatorcontrib><creatorcontrib>Unaleroglu, Canan</creatorcontrib><title>A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine</title><title>Tetrahedron letters</title><description>The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions. The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions.</description><subject>Catalysis</subject><subject>Catalysts</subject><subject>Expanded porphyrin</subject><subject>Hexaphyrin</subject><subject>N-sulfonyl aldimine</subject><subject>Synthesis (chemistry)</subject><subject>Tetrahedrons</subject><subject>Tripyrrane</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9UMFKxDAUDKLguvoHHnL00po0bZN6EJbFVWHRi55EQpq8uFm67Zpk1f69LfXsO7yBYWZgBqFLSlJKaHm9TSPEBmKaEcpSSkf2CM2o4CxhhaDHaEZITpKcsOoUnYWwJcOVgszQaoFb-MYe1Ae0EdvO47gBHPp2gOAC7ix-y8r3Dfyo_ab3rr3BT0k4NLZr-warxrida-EcnVjVBLj4wzl6Xd29LB-S9fP943KxTjRjVUxMTTRXtKzrWhRGCMOBc65EDYRk1GYKirLIrFC1qggzytKyzCsNWW6sZsawObqacve--zxAiHLngoamUS10hyApz3NOiuEP0nySat-F4MHKvXc75XtJiRxnk1s5zSbH2SSlIzvYbicbDDW-HHgZtINWg3EedJSmc_8H_AJDDXiF</recordid><startdate>20140108</startdate><enddate>20140108</enddate><creator>Cinar, Seda</creator><creator>Temelli, Baris</creator><creator>Unaleroglu, Canan</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20140108</creationdate><title>A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine</title><author>Cinar, Seda ; Temelli, Baris ; Unaleroglu, Canan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-db0c7a16bbb85d88d7e777a8be0021f2ae5652f8aba903daf16649ce24dfc3dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Catalysis</topic><topic>Catalysts</topic><topic>Expanded porphyrin</topic><topic>Hexaphyrin</topic><topic>N-sulfonyl aldimine</topic><topic>Synthesis (chemistry)</topic><topic>Tetrahedrons</topic><topic>Tripyrrane</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cinar, Seda</creatorcontrib><creatorcontrib>Temelli, Baris</creatorcontrib><creatorcontrib>Unaleroglu, Canan</creatorcontrib><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><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cinar, Seda</au><au>Temelli, Baris</au><au>Unaleroglu, Canan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine</atitle><jtitle>Tetrahedron letters</jtitle><date>2014-01-08</date><risdate>2014</risdate><volume>55</volume><issue>2</issue><spage>544</spage><epage>547</epage><pages>544-547</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions. The selective synthesis of [26]hexaphyrin(1.1.1.1.1.1) has been achieved by the reaction of meso-substituted tripyrrane and N-sulfonyl aldimine. The protocol is simple and requires only a catalytic amount of copper(II) triflate under mild reaction conditions.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tetlet.2013.11.101</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0040-4039
ispartof Tetrahedron letters, 2014-01, Vol.55 (2), p.544-547
issn 0040-4039
1873-3581
language eng
recordid cdi_proquest_miscellaneous_1744705744
source ScienceDirect Journals (5 years ago - present)
subjects Catalysis
Catalysts
Expanded porphyrin
Hexaphyrin
N-sulfonyl aldimine
Synthesis (chemistry)
Tetrahedrons
Tripyrrane
title A new reagent for the synthesis of [26]hexaphyrin: N-sulfonyl aldimine
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T21%3A01%3A33IST&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=A%20new%20reagent%20for%20the%20synthesis%20of%20%5B26%5Dhexaphyrin:%20N-sulfonyl%20aldimine&rft.jtitle=Tetrahedron%20letters&rft.au=Cinar,%20Seda&rft.date=2014-01-08&rft.volume=55&rft.issue=2&rft.spage=544&rft.epage=547&rft.pages=544-547&rft.issn=0040-4039&rft.eissn=1873-3581&rft_id=info:doi/10.1016/j.tetlet.2013.11.101&rft_dat=%3Cproquest_cross%3E1744705744%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=1744705744&rft_id=info:pmid/&rft_els_id=S0040403913020583&rfr_iscdi=true