Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f

Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f

A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that ena...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Laulhé, Sébastien, Blackburn, J. Miles, Roizen, Jennifer L
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 7273
container_issue 53
container_start_page 727
container_title
container_volume 53
creator Laulhé, Sébastien
Blackburn, J. Miles
Roizen, Jennifer L
description A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines.
doi_str_mv 10.1039/c7cc00997f
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c7cc00997f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c7cc00997f</sourcerecordid><originalsourceid>FETCH-rsc_primary_c7cc00997f3</originalsourceid><addsrcrecordid>eNp9kEFPwkAQhTdGExG9eDcZb5JYbFMqlKuUyAE14sEbGZapXVl2N7tbpP5of4MtmngwYS4zyfvy3sswdh6F3SiM0xve5zwM07SfH7BWFN_2gqQ3eD1s7iQN-nEvOWYnzr2H9UTJoMW-sm2BpfNiQzArP8uVCKaiwtIiWELuhVYOdA5Gy6pAqd9IoaclFOTJarSkyMGH8AWgXFUSFtpqJTgYoZBrCeRqzmWSuP8RXGmMpDUpj7YCoXJt19jEwFU2m3QANygkLiQNYVzK2mBryIodL2FJvlbdNXBtBO2KPUyfwZnGHuHqaTTudGFGBKPHyRD-f-WUHeUoHZ397ja7GGcvd_eBdXxu6py61PwPj9vscp8-N8uG2e_xDXoPhFY</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Laulhé, Sébastien ; Blackburn, J. Miles ; Roizen, Jennifer L</creator><creatorcontrib>Laulhé, Sébastien ; Blackburn, J. Miles ; Roizen, Jennifer L</creatorcontrib><description>A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c7cc00997f</identifier><language>eng</language><creationdate>2017-06</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Laulhé, Sébastien</creatorcontrib><creatorcontrib>Blackburn, J. Miles</creatorcontrib><creatorcontrib>Roizen, Jennifer L</creatorcontrib><title>Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f</title><description>A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNp9kEFPwkAQhTdGExG9eDcZb5JYbFMqlKuUyAE14sEbGZapXVl2N7tbpP5of4MtmngwYS4zyfvy3sswdh6F3SiM0xve5zwM07SfH7BWFN_2gqQ3eD1s7iQN-nEvOWYnzr2H9UTJoMW-sm2BpfNiQzArP8uVCKaiwtIiWELuhVYOdA5Gy6pAqd9IoaclFOTJarSkyMGH8AWgXFUSFtpqJTgYoZBrCeRqzmWSuP8RXGmMpDUpj7YCoXJt19jEwFU2m3QANygkLiQNYVzK2mBryIodL2FJvlbdNXBtBO2KPUyfwZnGHuHqaTTudGFGBKPHyRD-f-WUHeUoHZ397ja7GGcvd_eBdXxu6py61PwPj9vscp8-N8uG2e_xDXoPhFY</recordid><startdate>20170629</startdate><enddate>20170629</enddate><creator>Laulhé, Sébastien</creator><creator>Blackburn, J. Miles</creator><creator>Roizen, Jennifer L</creator><scope/></search><sort><creationdate>20170629</creationdate><title>Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f</title><author>Laulhé, Sébastien ; Blackburn, J. Miles ; Roizen, Jennifer L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c7cc00997f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laulhé, Sébastien</creatorcontrib><creatorcontrib>Blackburn, J. Miles</creatorcontrib><creatorcontrib>Roizen, Jennifer L</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laulhé, Sébastien</au><au>Blackburn, J. Miles</au><au>Roizen, Jennifer L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f</atitle><date>2017-06-29</date><risdate>2017</risdate><volume>53</volume><issue>53</issue><spage>727</spage><epage>7273</epage><pages>727-7273</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines.</abstract><doi>10.1039/c7cc00997f</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1359-7345
ispartof
issn 1359-7345
1364-548X
language eng
recordid cdi_rsc_primary_c7cc00997f
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T19%3A17%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Exhaustive%20Suzuki-Miyaura%20reactions%20of%20polyhalogenated%20heteroarenes%20with%20alkyl%20boronic%20pinacol%20estersElectronic%20supplementary%20information%20(ESI)%20available:%20Full%20experimental%20details,%20copies%20of%20NMR%20spectra%20(PDF).%20See%20DOI:%2010.1039/c7cc00997f&rft.au=Laulh%C3%A9,%20S%C3%A9bastien&rft.date=2017-06-29&rft.volume=53&rft.issue=53&rft.spage=727&rft.epage=7273&rft.pages=727-7273&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c7cc00997f&rft_dat=%3Crsc%3Ec7cc00997f%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true