ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes
The reaction of various aminonaphthalenes and phenothiazine with allyl acetate is first investigated and then extended to 1‐aminonaphthalene and different types of allylic acetate substrates.
Gespeichert in:
Veröffentlicht in: | ChemInform 2012-05, Vol.43 (20), p.no-no |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | no |
---|---|
container_issue | 20 |
container_start_page | no |
container_title | ChemInform |
container_volume | 43 |
creator | Shue, Yi-Jen Yang, Shyh-Chyun |
description | The reaction of various aminonaphthalenes and phenothiazine with allyl acetate is first investigated and then extended to 1‐aminonaphthalene and different types of allylic acetate substrates. |
doi_str_mv | 10.1002/chin.201220082 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1267097176</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2859623891</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1552-80dba205d7c6164e1f31daa970992a32fcc9dfbce90e36306c43b74dba00c6183</originalsourceid><addsrcrecordid>eNqF0M9P2zAUB3BrAolSduVsaecU_2jseLcugraiKpVglJvlOo5i5sSZnWorfz1GRYgbl_cu38970heAS4wmGCFypRvbTQjChCBUkG9ghHNCMsIYPwEjJCjOeC74GTiP8TnlKS_ICPRlY9plV_vQwtkuDkHp4Se8t23vDNwo51Rl921WqkG5w4upYJmt4S_fVfAmETVY38GE4cansd5rZ3zfWGe1HQ7Q13DW2s53qm-GRjnTmXgBTmvlovn-vsfg9831Q7nIVnfzZTlbZRrnOckKVO0UQXnFNcNsanBNcaWU4EgIoiiptRZVvdNGIEMZRUxP6Y5PE0IoiYKOwY_j3T74v3sTB_ns96FLLyUmLJ3hmLOUmhxTOvgYg6llH2yrwkFiJN9alW-tyo9WExBH8M86c_giLcvFcv3ZZkdr42D-f1gV_kjGKc_ldj2XC8E2xdPjVt7SV4v-i8g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1267097176</pqid></control><display><type>article</type><title>ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes</title><source>Wiley Journals</source><creator>Shue, Yi-Jen ; Yang, Shyh-Chyun</creator><creatorcontrib>Shue, Yi-Jen ; Yang, Shyh-Chyun</creatorcontrib><description>The reaction of various aminonaphthalenes and phenothiazine with allyl acetate is first investigated and then extended to 1‐aminonaphthalene and different types of allylic acetate substrates.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201220082</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>amination ; amination, N‐alkylation, N‐arylation ; amines (naphthalene compounds) ; N-alkylation ; N-arylation</subject><ispartof>ChemInform, 2012-05, Vol.43 (20), p.no-no</ispartof><rights>Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1552-80dba205d7c6164e1f31daa970992a32fcc9dfbce90e36306c43b74dba00c6183</cites></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.201220082$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.201220082$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Shue, Yi-Jen</creatorcontrib><creatorcontrib>Yang, Shyh-Chyun</creatorcontrib><title>ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes</title><title>ChemInform</title><addtitle>ChemInform</addtitle><description>The reaction of various aminonaphthalenes and phenothiazine with allyl acetate is first investigated and then extended to 1‐aminonaphthalene and different types of allylic acetate substrates.</description><subject>amination</subject><subject>amination, N‐alkylation, N‐arylation</subject><subject>amines (naphthalene compounds)</subject><subject>N-alkylation</subject><subject>N-arylation</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqF0M9P2zAUB3BrAolSduVsaecU_2jseLcugraiKpVglJvlOo5i5sSZnWorfz1GRYgbl_cu38970heAS4wmGCFypRvbTQjChCBUkG9ghHNCMsIYPwEjJCjOeC74GTiP8TnlKS_ICPRlY9plV_vQwtkuDkHp4Se8t23vDNwo51Rl921WqkG5w4upYJmt4S_fVfAmETVY38GE4cansd5rZ3zfWGe1HQ7Q13DW2s53qm-GRjnTmXgBTmvlovn-vsfg9831Q7nIVnfzZTlbZRrnOckKVO0UQXnFNcNsanBNcaWU4EgIoiiptRZVvdNGIEMZRUxP6Y5PE0IoiYKOwY_j3T74v3sTB_ns96FLLyUmLJ3hmLOUmhxTOvgYg6llH2yrwkFiJN9alW-tyo9WExBH8M86c_giLcvFcv3ZZkdr42D-f1gV_kjGKc_ldj2XC8E2xdPjVt7SV4v-i8g</recordid><startdate>20120515</startdate><enddate>20120515</enddate><creator>Shue, Yi-Jen</creator><creator>Yang, Shyh-Chyun</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20120515</creationdate><title>ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes</title><author>Shue, Yi-Jen ; Yang, Shyh-Chyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1552-80dba205d7c6164e1f31daa970992a32fcc9dfbce90e36306c43b74dba00c6183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>amination</topic><topic>amination, N‐alkylation, N‐arylation</topic><topic>amines (naphthalene compounds)</topic><topic>N-alkylation</topic><topic>N-arylation</topic><toplevel>online_resources</toplevel><creatorcontrib>Shue, Yi-Jen</creatorcontrib><creatorcontrib>Yang, Shyh-Chyun</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shue, Yi-Jen</au><au>Yang, Shyh-Chyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes</atitle><jtitle>ChemInform</jtitle><addtitle>ChemInform</addtitle><date>2012-05-15</date><risdate>2012</risdate><volume>43</volume><issue>20</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>The reaction of various aminonaphthalenes and phenothiazine with allyl acetate is first investigated and then extended to 1‐aminonaphthalene and different types of allylic acetate substrates.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/chin.201220082</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0931-7597 |
ispartof | ChemInform, 2012-05, Vol.43 (20), p.no-no |
issn | 0931-7597 1522-2667 |
language | eng |
recordid | cdi_proquest_journals_1267097176 |
source | Wiley Journals |
subjects | amination amination, N‐alkylation, N‐arylation amines (naphthalene compounds) N-alkylation N-arylation |
title | ChemInform Abstract: Simple Palladium-Catalyzed C-N Bond Formation for Poor Nucleophilicity of Aminonaphthalenes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T06%3A36%3A20IST&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=ChemInform%20Abstract:%20Simple%20Palladium-Catalyzed%20C-N%20Bond%20Formation%20for%20Poor%20Nucleophilicity%20of%20Aminonaphthalenes&rft.jtitle=ChemInform&rft.au=Shue,%20Yi-Jen&rft.date=2012-05-15&rft.volume=43&rft.issue=20&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.201220082&rft_dat=%3Cproquest_cross%3E2859623891%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=1267097176&rft_id=info:pmid/&rfr_iscdi=true |