Loading…
A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one
A facile and efficient synthetic strategy to 3-((trifluoromethyl)thio)-4H-chromen-4-one was developed. AgSCF3 and trichloroisocyanuric acid were employed here to generate active electrophilic trifluoromethylthio species in situ. This reaction could proceed under mild conditions in a short reacti...
Saved in:
Published in: | Organic letters 2014-11, Vol.16 (21), p.5686-5689 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 5689 |
container_issue | 21 |
container_start_page | 5686 |
container_title | Organic letters |
container_volume | 16 |
creator | Xiang, Haoyue Yang, Chunhao |
description | A facile and efficient synthetic strategy to 3-((trifluoromethyl)thio)-4H-chromen-4-one was developed. AgSCF3 and trichloroisocyanuric acid were employed here to generate active electrophilic trifluoromethylthio species in situ. This reaction could proceed under mild conditions in a short reaction time and be insensitive to air and moisture. |
doi_str_mv | 10.1021/ol502751k |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1622065127</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1622065127</sourcerecordid><originalsourceid>FETCH-LOGICAL-a237t-82eb447feee13fcb37728403c29acd772255903929cb6df83110587ce58a365c3</originalsourceid><addsrcrecordid>eNo9kD1OwzAYhi0EoqUwcAGUBakdAv6J42SsKtoiVWJpZ8txvigpTlycZOjGFThIL9GjcBKMCl2-30evXr0I3RP8RDAlz9ZwTAUn7xdoSDhlocCcXp7nGA_QTdtuMSb-kl6jAeWMJTQlQ7SZBnOlKwOBavJgAQ04ZYLpbues0mXQ2YB9f36Nx2tXFaa3zh4PNXTl3kyOh66s7MR_o6UvunS2hiaMQtvALboqlGnh7q-P0Gb-sp4tw9Xb4nU2XYWKMtGFCYUsikQBAIQVOmNC0CTCTNNU6dwvlPMUs5SmOovzImGEYJ4IDTxRLOaajdD4pOvtfvTQdrKuWg3GqAZs30oSU4pjTqjw6MMf2mc15HLnqlq5vfyPwgOPJ0DpVm5t7xrvXBIsfyOW54jZD4A-bQg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1622065127</pqid></control><display><type>article</type><title>A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Xiang, Haoyue ; Yang, Chunhao</creator><creatorcontrib>Xiang, Haoyue ; Yang, Chunhao</creatorcontrib><description>A facile and efficient synthetic strategy to 3-((trifluoromethyl)thio)-4H-chromen-4-one was developed. AgSCF3 and trichloroisocyanuric acid were employed here to generate active electrophilic trifluoromethylthio species in situ. This reaction could proceed under mild conditions in a short reaction time and be insensitive to air and moisture.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol502751k</identifier><identifier>PMID: 25338291</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Catalysis ; Chromones - chemical synthesis ; Chromones - chemistry ; Hydrocarbons, Halogenated - chemistry ; Molecular Structure ; Silver - chemistry ; Triazines - chemistry</subject><ispartof>Organic letters, 2014-11, Vol.16 (21), p.5686-5689</ispartof><rights>Copyright © 2014 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25338291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiang, Haoyue</creatorcontrib><creatorcontrib>Yang, Chunhao</creatorcontrib><title>A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>A facile and efficient synthetic strategy to 3-((trifluoromethyl)thio)-4H-chromen-4-one was developed. AgSCF3 and trichloroisocyanuric acid were employed here to generate active electrophilic trifluoromethylthio species in situ. This reaction could proceed under mild conditions in a short reaction time and be insensitive to air and moisture.</description><subject>Catalysis</subject><subject>Chromones - chemical synthesis</subject><subject>Chromones - chemistry</subject><subject>Hydrocarbons, Halogenated - chemistry</subject><subject>Molecular Structure</subject><subject>Silver - chemistry</subject><subject>Triazines - chemistry</subject><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo9kD1OwzAYhi0EoqUwcAGUBakdAv6J42SsKtoiVWJpZ8txvigpTlycZOjGFThIL9GjcBKMCl2-30evXr0I3RP8RDAlz9ZwTAUn7xdoSDhlocCcXp7nGA_QTdtuMSb-kl6jAeWMJTQlQ7SZBnOlKwOBavJgAQ04ZYLpbues0mXQ2YB9f36Nx2tXFaa3zh4PNXTl3kyOh66s7MR_o6UvunS2hiaMQtvALboqlGnh7q-P0Gb-sp4tw9Xb4nU2XYWKMtGFCYUsikQBAIQVOmNC0CTCTNNU6dwvlPMUs5SmOovzImGEYJ4IDTxRLOaajdD4pOvtfvTQdrKuWg3GqAZs30oSU4pjTqjw6MMf2mc15HLnqlq5vfyPwgOPJ0DpVm5t7xrvXBIsfyOW54jZD4A-bQg</recordid><startdate>20141107</startdate><enddate>20141107</enddate><creator>Xiang, Haoyue</creator><creator>Yang, Chunhao</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20141107</creationdate><title>A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one</title><author>Xiang, Haoyue ; Yang, Chunhao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a237t-82eb447feee13fcb37728403c29acd772255903929cb6df83110587ce58a365c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Catalysis</topic><topic>Chromones - chemical synthesis</topic><topic>Chromones - chemistry</topic><topic>Hydrocarbons, Halogenated - chemistry</topic><topic>Molecular Structure</topic><topic>Silver - chemistry</topic><topic>Triazines - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiang, Haoyue</creatorcontrib><creatorcontrib>Yang, Chunhao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiang, Haoyue</au><au>Yang, Chunhao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2014-11-07</date><risdate>2014</risdate><volume>16</volume><issue>21</issue><spage>5686</spage><epage>5689</epage><pages>5686-5689</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>A facile and efficient synthetic strategy to 3-((trifluoromethyl)thio)-4H-chromen-4-one was developed. AgSCF3 and trichloroisocyanuric acid were employed here to generate active electrophilic trifluoromethylthio species in situ. This reaction could proceed under mild conditions in a short reaction time and be insensitive to air and moisture.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25338291</pmid><doi>10.1021/ol502751k</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1523-7060 |
ispartof | Organic letters, 2014-11, Vol.16 (21), p.5686-5689 |
issn | 1523-7060 1523-7052 |
language | eng |
recordid | cdi_proquest_miscellaneous_1622065127 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Catalysis Chromones - chemical synthesis Chromones - chemistry Hydrocarbons, Halogenated - chemistry Molecular Structure Silver - chemistry Triazines - chemistry |
title | A Facile and General Approach to 3‑((Trifluoromethyl)thio)‑4H‑chromen-4-one |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T23%3A06%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Facile%20and%20General%20Approach%20to%203%E2%80%91((Trifluoro%C2%ADmethyl)%C2%ADthio)%E2%80%914H%E2%80%91chromen-4-one&rft.jtitle=Organic%20letters&rft.au=Xiang,%20Haoyue&rft.date=2014-11-07&rft.volume=16&rft.issue=21&rft.spage=5686&rft.epage=5689&rft.pages=5686-5689&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol502751k&rft_dat=%3Cproquest_pubme%3E1622065127%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a237t-82eb447feee13fcb37728403c29acd772255903929cb6df83110587ce58a365c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1622065127&rft_id=info:pmid/25338291&rfr_iscdi=true |