Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes

Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient sol...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the Chinese Chemical Society (Taipei) 2008-08, Vol.55 (4), p.871-874
Hauptverfasser: Khansole, Sandeep V., Mokle, Shyam S., Sayyed, Mudassar A., Vibhute, Yeshwant B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 874
container_issue 4
container_start_page 871
container_title Journal of the Chinese Chemical Society (Taipei)
container_volume 55
creator Khansole, Sandeep V.
Mokle, Shyam S.
Sayyed, Mudassar A.
Vibhute, Yeshwant B.
description Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely. Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely.
doi_str_mv 10.1002/jccs.200800130
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jccs_200800130</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JCCS200800130</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3230-a5902be6af16dde2c5b48a872d3ed39715cec7eef3dbd2f99d3f67ca566696093</originalsourceid><addsrcrecordid>eNqFkEtPAyEUhYnRxFrduuYPTL0DhSnuaqP1FTU-4pJQuCjtdDAwRuff26amcefqJOee7y4-Qo5LGJQA7GRubR4wgBFAyWGH9FipWCHFUO2SHgCoYii43CcHOc8BhpwJ1SOLhy4FF5rwuaRX0UX7XsdVgad03NBz74MN2LT0Ec3bOn1M61loTBtiQ6Onl51L8burTYuOjlNcri6W3mAbG8zUNKuydvjeOcyHZM-bOuPRb_bJy8X58-SyuL2fXk3Gt4XljENhhAI2Q2l8KZ1DZsVsODKjijmOjquqFBZthei5mznmlXLcy8oaIaVUEhTvk8Hmr00x54Ref6SwNKnTJei1Kr1WpbeqVoDaAF-hxu6ftb6eTJ7-ssWGDbnF7y1r0kLLildCv95N9dk1u-OCV3rKfwBGvX6D</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Khansole, Sandeep V. ; Mokle, Shyam S. ; Sayyed, Mudassar A. ; Vibhute, Yeshwant B.</creator><creatorcontrib>Khansole, Sandeep V. ; Mokle, Shyam S. ; Sayyed, Mudassar A. ; Vibhute, Yeshwant B.</creatorcontrib><description>Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely. Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.200800130</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Aromatic acetophenones ; Aromatic aldehydes ; Iodination ; Pyridinium iodochloride</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2008-08, Vol.55 (4), p.871-874</ispartof><rights>Copyright © 2008 The Chemical Society Located in Taipei &amp; Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim, Germany</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3230-a5902be6af16dde2c5b48a872d3ed39715cec7eef3dbd2f99d3f67ca566696093</citedby><cites>FETCH-LOGICAL-c3230-a5902be6af16dde2c5b48a872d3ed39715cec7eef3dbd2f99d3f67ca566696093</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%2Fjccs.200800130$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjccs.200800130$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Khansole, Sandeep V.</creatorcontrib><creatorcontrib>Mokle, Shyam S.</creatorcontrib><creatorcontrib>Sayyed, Mudassar A.</creatorcontrib><creatorcontrib>Vibhute, Yeshwant B.</creatorcontrib><title>Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes</title><title>Journal of the Chinese Chemical Society (Taipei)</title><addtitle>Jnl Chinese Chemical Soc</addtitle><description>Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely. Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely.</description><subject>Aromatic acetophenones</subject><subject>Aromatic aldehydes</subject><subject>Iodination</subject><subject>Pyridinium iodochloride</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPAyEUhYnRxFrduuYPTL0DhSnuaqP1FTU-4pJQuCjtdDAwRuff26amcefqJOee7y4-Qo5LGJQA7GRubR4wgBFAyWGH9FipWCHFUO2SHgCoYii43CcHOc8BhpwJ1SOLhy4FF5rwuaRX0UX7XsdVgad03NBz74MN2LT0Ec3bOn1M61loTBtiQ6Onl51L8burTYuOjlNcri6W3mAbG8zUNKuydvjeOcyHZM-bOuPRb_bJy8X58-SyuL2fXk3Gt4XljENhhAI2Q2l8KZ1DZsVsODKjijmOjquqFBZthei5mznmlXLcy8oaIaVUEhTvk8Hmr00x54Ref6SwNKnTJei1Kr1WpbeqVoDaAF-hxu6ftb6eTJ7-ssWGDbnF7y1r0kLLildCv95N9dk1u-OCV3rKfwBGvX6D</recordid><startdate>200808</startdate><enddate>200808</enddate><creator>Khansole, Sandeep V.</creator><creator>Mokle, Shyam S.</creator><creator>Sayyed, Mudassar A.</creator><creator>Vibhute, Yeshwant B.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200808</creationdate><title>Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes</title><author>Khansole, Sandeep V. ; Mokle, Shyam S. ; Sayyed, Mudassar A. ; Vibhute, Yeshwant B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3230-a5902be6af16dde2c5b48a872d3ed39715cec7eef3dbd2f99d3f67ca566696093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aromatic acetophenones</topic><topic>Aromatic aldehydes</topic><topic>Iodination</topic><topic>Pyridinium iodochloride</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khansole, Sandeep V.</creatorcontrib><creatorcontrib>Mokle, Shyam S.</creatorcontrib><creatorcontrib>Sayyed, Mudassar A.</creatorcontrib><creatorcontrib>Vibhute, Yeshwant B.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khansole, Sandeep V.</au><au>Mokle, Shyam S.</au><au>Sayyed, Mudassar A.</au><au>Vibhute, Yeshwant B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><addtitle>Jnl Chinese Chemical Soc</addtitle><date>2008-08</date><risdate>2008</risdate><volume>55</volume><issue>4</issue><spage>871</spage><epage>874</epage><pages>871-874</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely. Direct iodination of several reactive aromatic compounds like hydroxy substituted acetophenones and aldehydes with pyridinium iodochloride (PyICl) proceeded smoothly to afford the corresponding aromatic iodides in good to excellent yield. Pyridinium iodochloride has been found to be an efficient solid iodinating reagent with no hazardous effect and it can be handled safely.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/jccs.200800130</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0009-4536
ispartof Journal of the Chinese Chemical Society (Taipei), 2008-08, Vol.55 (4), p.871-874
issn 0009-4536
2192-6549
language eng
recordid cdi_crossref_primary_10_1002_jccs_200800130
source Wiley Online Library Journals Frontfile Complete
subjects Aromatic acetophenones
Aromatic aldehydes
Iodination
Pyridinium iodochloride
title Pyridinium Iodochloride: An Efficient Reagent for Iodination of Hydroxylated Aromatic Ketones and Aldehydes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T03%3A02%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pyridinium%20Iodochloride:%20An%20Efficient%20Reagent%20for%20Iodination%20of%20Hydroxylated%20Aromatic%20Ketones%20and%20Aldehydes&rft.jtitle=Journal%20of%20the%20Chinese%20Chemical%20Society%20(Taipei)&rft.au=Khansole,%20Sandeep%20V.&rft.date=2008-08&rft.volume=55&rft.issue=4&rft.spage=871&rft.epage=874&rft.pages=871-874&rft.issn=0009-4536&rft.eissn=2192-6549&rft_id=info:doi/10.1002/jccs.200800130&rft_dat=%3Cwiley_cross%3EJCCS200800130%3C/wiley_cross%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