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Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water
Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA)...
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Published in: | Synthetic communications 2021-05, Vol.51 (10), p.1581-1587 |
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container_title | Synthetic communications |
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creator | Jia, Jia Su, Ye Yu, Hai-Feng Du, Hai-Tao Mei, Ze-Min |
description | Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA) in boiling water, β-ethyltho-β-indolyl-α, β-unsaturated ketones efficiently reacted with hydroxylamine hydrochloride to afford 3-(isoxazol-5)-yl)indoles in good yields and with good to excellent regioselectivity. The method features the advantages of eco-friendly process, good yield and regioselevtivity, operational simplicity, broad substrate scope and ease of scale-up. |
doi_str_mv | 10.1080/00397911.2021.1894339 |
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It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA) in boiling water, β-ethyltho-β-indolyl-α, β-unsaturated ketones efficiently reacted with hydroxylamine hydrochloride to afford 3-(isoxazol-5)-yl)indoles in good yields and with good to excellent regioselectivity. The method features the advantages of eco-friendly process, good yield and regioselevtivity, operational simplicity, broad substrate scope and ease of scale-up.</description><identifier>ISSN: 0039-7911</identifier><identifier>EISSN: 1532-2432</identifier><identifier>DOI: 10.1080/00397911.2021.1894339</identifier><language>eng</language><publisher>Philadelphia: Taylor & Francis</publisher><subject>3-isoxazolindoles ; Aqueous synthesis ; hydroxylamine hydro-chloride ; Indoles ; Ketones ; Regioselectivity ; Substrates ; Sulfonic acid ; Synthesis ; β-ethylthio-β-indolyl-α ; β-unsaturatedketones</subject><ispartof>Synthetic communications, 2021-05, Vol.51 (10), p.1581-1587</ispartof><rights>2021 Taylor & Francis Group, LLC 2021</rights><rights>2021 Taylor & Francis Group, LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c338t-64231ef161f4084736019c178f4b858bfad439ae726013a0c943d9fbd44d882e3</citedby><cites>FETCH-LOGICAL-c338t-64231ef161f4084736019c178f4b858bfad439ae726013a0c943d9fbd44d882e3</cites></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></links><search><creatorcontrib>Jia, Jia</creatorcontrib><creatorcontrib>Su, Ye</creatorcontrib><creatorcontrib>Yu, Hai-Feng</creatorcontrib><creatorcontrib>Du, Hai-Tao</creatorcontrib><creatorcontrib>Mei, Ze-Min</creatorcontrib><title>Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water</title><title>Synthetic communications</title><description>Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA) in boiling water, β-ethyltho-β-indolyl-α, β-unsaturated ketones efficiently reacted with hydroxylamine hydrochloride to afford 3-(isoxazol-5)-yl)indoles in good yields and with good to excellent regioselectivity. The method features the advantages of eco-friendly process, good yield and regioselevtivity, operational simplicity, broad substrate scope and ease of scale-up.</description><subject>3-isoxazolindoles</subject><subject>Aqueous synthesis</subject><subject>hydroxylamine hydro-chloride</subject><subject>Indoles</subject><subject>Ketones</subject><subject>Regioselectivity</subject><subject>Substrates</subject><subject>Sulfonic acid</subject><subject>Synthesis</subject><subject>β-ethylthio-β-indolyl-α</subject><subject>β-unsaturatedketones</subject><issn>0039-7911</issn><issn>1532-2432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OGzEUhS0EEmnoIyBZ6qZIOPXfzHh2rRC0SEjdwNpyxjZx6tip7QDDM_Ay8CA8U2eSdMvq6txzzr3SB8ApwTOCBf6GMWublpAZxZTMiGg5Y-0BmJCKUUQ5o4dgMmbQGDoGn3JeYkyqRrQT8HLZRWSTM0H7HqqgYTL3LmbjTVfcg4G5D2VhssswWsjQV5fjk3qOHlVnqPdn0AUdvcnQpriC728QmbLofVm4iLZy6_cevb-eb_UmZFU2SRWj4R9TYhi6LsDHYZFOwJFVPpvP-zkFd1eXtxe_0M3vn9cXP25Qx5goqOaUEWNJTSzHgjesxqTtSCMsn4tKzK3SnLXKNHQwmMLdAES3dq4510JQw6bgy-7uOsW_G5OLXMZNCsNLSStS45phUg-papfqUsw5GSvXya1U6iXBcgQv_4OXI3i5Bz_0vu96LtiYVuoxJq9lUb2PySYVOpcl-_jEP5QrjKc</recordid><startdate>20210519</startdate><enddate>20210519</enddate><creator>Jia, Jia</creator><creator>Su, Ye</creator><creator>Yu, Hai-Feng</creator><creator>Du, Hai-Tao</creator><creator>Mei, Ze-Min</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20210519</creationdate><title>Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water</title><author>Jia, Jia ; Su, Ye ; Yu, Hai-Feng ; Du, Hai-Tao ; Mei, Ze-Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-64231ef161f4084736019c178f4b858bfad439ae726013a0c943d9fbd44d882e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>3-isoxazolindoles</topic><topic>Aqueous synthesis</topic><topic>hydroxylamine hydro-chloride</topic><topic>Indoles</topic><topic>Ketones</topic><topic>Regioselectivity</topic><topic>Substrates</topic><topic>Sulfonic acid</topic><topic>Synthesis</topic><topic>β-ethylthio-β-indolyl-α</topic><topic>β-unsaturatedketones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jia, Jia</creatorcontrib><creatorcontrib>Su, Ye</creatorcontrib><creatorcontrib>Yu, Hai-Feng</creatorcontrib><creatorcontrib>Du, Hai-Tao</creatorcontrib><creatorcontrib>Mei, Ze-Min</creatorcontrib><collection>CrossRef</collection><jtitle>Synthetic communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jia, Jia</au><au>Su, Ye</au><au>Yu, Hai-Feng</au><au>Du, Hai-Tao</au><au>Mei, Ze-Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water</atitle><jtitle>Synthetic communications</jtitle><date>2021-05-19</date><risdate>2021</risdate><volume>51</volume><issue>10</issue><spage>1581</spage><epage>1587</epage><pages>1581-1587</pages><issn>0039-7911</issn><eissn>1532-2432</eissn><abstract>Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. 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source | Taylor and Francis Science and Technology Collection |
subjects | 3-isoxazolindoles Aqueous synthesis hydroxylamine hydro-chloride Indoles Ketones Regioselectivity Substrates Sulfonic acid Synthesis β-ethylthio-β-indolyl-α β-unsaturatedketones |
title | Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water |
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