Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals

Acetals and ketals are readily deprotected under neutral conditions in the presence of acetone and catalytic amounts of indium(III) trifluoromethanesulfonate (

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of organic chemistry 2007-07, Vol.72 (15), p.5890-5893
Hauptverfasser: Gregg, Brian T, Golden, Kathryn C, Quinn, John F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5893
container_issue 15
container_start_page 5890
container_title Journal of organic chemistry
container_volume 72
creator Gregg, Brian T
Golden, Kathryn C
Quinn, John F
description Acetals and ketals are readily deprotected under neutral conditions in the presence of acetone and catalytic amounts of indium(III) trifluoromethanesulfonate (
doi_str_mv 10.1021/jo0707075
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70706556</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70706556</sourcerecordid><originalsourceid>FETCH-LOGICAL-a381t-2e4eda8296be68845ceb904447aa440f7fda170248cdb3b00d702cbb6fb398dd3</originalsourceid><addsrcrecordid>eNptkE9PHSEUxYmx0Vfrol_AsLGpi7EwwPxZ2qfVsSZt0mfSHWHgEtGZQYFJ6rcvr-_Ft-llcSH3x8m5B6GPlJxTUtIvj57U6yP20IKKkhRVS_g-WhBSlgUrK3aI3sf4SHIJIQ7QIa1FKyhrF8h1k3Hz-LnrujO8Cs4Osw9-hPSgJojzYP2kEmAVsZrwlbVOO5gSXqqkhteYsPUBpwfAl_AcfAKdnJ-wt_hCQybWvwz-_u_6Ab2zucHxth-h-29Xq-VNcffjulte3BWKNTQVJXAwqinbqoeqabjQ0OdtOK-V4pzY2hpFa1LyRpue9YSY_NB9X9metY0x7Ah92uhmQy8zxCRHFzUMQ17Iz1Guk6qEqDJ4tgF18DEGsPI5uFGFV0mJXOcq33LN7MlWdO5HMDtyG2QGTreAiloNNqhJu7jjmpYLQurMFRvOxQR_3uYqPMmqZrWQq5-_JL-kt8uvv5mkO12lY_Yzhyln9x-DfwFBDJrQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70706556</pqid></control><display><type>article</type><title>Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals</title><source>ACS Publications</source><source>MEDLINE</source><creator>Gregg, Brian T ; Golden, Kathryn C ; Quinn, John F</creator><creatorcontrib>Gregg, Brian T ; Golden, Kathryn C ; Quinn, John F</creatorcontrib><description>Acetals and ketals are readily deprotected under neutral conditions in the presence of acetone and catalytic amounts of indium(III) trifluoromethanesulfonate (&lt;0.8 mol %) at room temperature or mild microwave heating conditions to give the corresponding aldehydes and ketones in good to excellent yields.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo0707075</identifier><identifier>PMID: 17595139</identifier><identifier>CODEN: JOCEAH</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Acetals - chemistry ; Catalysis ; Catalysts: preparations and properties ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Magnetic Resonance Spectroscopy ; Organic chemistry ; Organometallic Compounds - chemistry ; Spectrometry, Mass, Electrospray Ionization ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Journal of organic chemistry, 2007-07, Vol.72 (15), p.5890-5893</ispartof><rights>Copyright © 2007 American Chemical Society</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-2e4eda8296be68845ceb904447aa440f7fda170248cdb3b00d702cbb6fb398dd3</citedby><cites>FETCH-LOGICAL-a381t-2e4eda8296be68845ceb904447aa440f7fda170248cdb3b00d702cbb6fb398dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jo0707075$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jo0707075$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18945007$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17595139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gregg, Brian T</creatorcontrib><creatorcontrib>Golden, Kathryn C</creatorcontrib><creatorcontrib>Quinn, John F</creatorcontrib><title>Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Acetals and ketals are readily deprotected under neutral conditions in the presence of acetone and catalytic amounts of indium(III) trifluoromethanesulfonate (&lt;0.8 mol %) at room temperature or mild microwave heating conditions to give the corresponding aldehydes and ketones in good to excellent yields.</description><subject>Acetals - chemistry</subject><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Organic chemistry</subject><subject>Organometallic Compounds - chemistry</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE9PHSEUxYmx0Vfrol_AsLGpi7EwwPxZ2qfVsSZt0mfSHWHgEtGZQYFJ6rcvr-_Ft-llcSH3x8m5B6GPlJxTUtIvj57U6yP20IKKkhRVS_g-WhBSlgUrK3aI3sf4SHIJIQ7QIa1FKyhrF8h1k3Hz-LnrujO8Cs4Osw9-hPSgJojzYP2kEmAVsZrwlbVOO5gSXqqkhteYsPUBpwfAl_AcfAKdnJ-wt_hCQybWvwz-_u_6Ab2zucHxth-h-29Xq-VNcffjulte3BWKNTQVJXAwqinbqoeqabjQ0OdtOK-V4pzY2hpFa1LyRpue9YSY_NB9X9metY0x7Ah92uhmQy8zxCRHFzUMQ17Iz1Guk6qEqDJ4tgF18DEGsPI5uFGFV0mJXOcq33LN7MlWdO5HMDtyG2QGTreAiloNNqhJu7jjmpYLQurMFRvOxQR_3uYqPMmqZrWQq5-_JL-kt8uvv5mkO12lY_Yzhyln9x-DfwFBDJrQ</recordid><startdate>20070720</startdate><enddate>20070720</enddate><creator>Gregg, Brian T</creator><creator>Golden, Kathryn C</creator><creator>Quinn, John F</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070720</creationdate><title>Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals</title><author>Gregg, Brian T ; Golden, Kathryn C ; Quinn, John F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-2e4eda8296be68845ceb904447aa440f7fda170248cdb3b00d702cbb6fb398dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Acetals - chemistry</topic><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Organic chemistry</topic><topic>Organometallic Compounds - chemistry</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gregg, Brian T</creatorcontrib><creatorcontrib>Golden, Kathryn C</creatorcontrib><creatorcontrib>Quinn, John F</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gregg, Brian T</au><au>Golden, Kathryn C</au><au>Quinn, John F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2007-07-20</date><risdate>2007</risdate><volume>72</volume><issue>15</issue><spage>5890</spage><epage>5893</epage><pages>5890-5893</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>Acetals and ketals are readily deprotected under neutral conditions in the presence of acetone and catalytic amounts of indium(III) trifluoromethanesulfonate (&lt;0.8 mol %) at room temperature or mild microwave heating conditions to give the corresponding aldehydes and ketones in good to excellent yields.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17595139</pmid><doi>10.1021/jo0707075</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3263
ispartof Journal of organic chemistry, 2007-07, Vol.72 (15), p.5890-5893
issn 0022-3263
1520-6904
language eng
recordid cdi_proquest_miscellaneous_70706556
source ACS Publications; MEDLINE
subjects Acetals - chemistry
Catalysis
Catalysts: preparations and properties
Chemistry
Exact sciences and technology
General and physical chemistry
Magnetic Resonance Spectroscopy
Organic chemistry
Organometallic Compounds - chemistry
Spectrometry, Mass, Electrospray Ionization
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Indium(III) Trifluoromethanesulfonate as an Efficient Catalyst for the Deprotection of Acetals and Ketals
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T14%3A18%3A27IST&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=Indium(III)%20Trifluoromethanesulfonate%20as%20an%20Efficient%20Catalyst%20for%20the%20Deprotection%20of%20Acetals%20and%20Ketals&rft.jtitle=Journal%20of%20organic%20chemistry&rft.au=Gregg,%20Brian%20T&rft.date=2007-07-20&rft.volume=72&rft.issue=15&rft.spage=5890&rft.epage=5893&rft.pages=5890-5893&rft.issn=0022-3263&rft.eissn=1520-6904&rft.coden=JOCEAH&rft_id=info:doi/10.1021/jo0707075&rft_dat=%3Cproquest_cross%3E70706556%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=70706556&rft_id=info:pmid/17595139&rfr_iscdi=true