Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach
Our recently reported novel green chemistry tool was effectively used for opening cyclic ethers to produce alpha -iodo- and bromoalkanols. The synthesis of 4-iodobutanoic acid from gamma -butyrolactone has also been described. The method is based on the use of a dried Dowex H super(+)/NaX (X = Br, I...
Gespeichert in:
Veröffentlicht in: | RSC advances 2016-02, Vol.6 (19), p.15937-15940 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15940 |
---|---|
container_issue | 19 |
container_start_page | 15937 |
container_title | RSC advances |
container_volume | 6 |
creator | Turhanen, Petri A Vepsaelaeinen, Jouko J |
description | Our recently reported novel green chemistry tool was effectively used for opening cyclic ethers to produce alpha -iodo- and bromoalkanols. The synthesis of 4-iodobutanoic acid from gamma -butyrolactone has also been described. The method is based on the use of a dried Dowex H super(+)/NaX (X = Br, I)-system, which is effective at producing alpha -iodoalkanols and some alpha -bromoalkanols from commercially available cyclic ethers. Additionally, opening of three different crown ethers to form alpha -iodo(polyethylene)glycols with various chain lengths is demonstrated. Haloalkanols are important building blocks in synthetic chemistry e.g. for medicinal chemistry purposes. |
doi_str_mv | 10.1039/c5ra20813k |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1800460001</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1800460001</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_18004600013</originalsourceid><addsrcrecordid>eNqVT8tOwzAQtJCQqKAXvmCPqWiondCoPXDhpXJBPfTQW7VxHGLieoM3FvAPfDRG4geYy8xoZlcaIS6VvFayXC_0MmAhV6rsT8SkkDdVXshqfSamzG8yoVqqolIT8b0NZsCAoyUP1EJk00YHdbSusf4Vake65zmgGzqE3FJDOaBvoA50JHQ9enIMbXKgv7SzGszYmcDp0-990vBAH-YTNsBxMCG7mi1ecA_ZHm7heQ53YQY4DIFQdxfitEXHZvrH5yJ7etzdb_IUv0fD4-FoWRvn0BuKfFArmZalNar8R_UHZ0JanQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1800460001</pqid></control><display><type>article</type><title>Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach</title><source>Royal Society Of Chemistry Journals</source><creator>Turhanen, Petri A ; Vepsaelaeinen, Jouko J</creator><creatorcontrib>Turhanen, Petri A ; Vepsaelaeinen, Jouko J</creatorcontrib><description>Our recently reported novel green chemistry tool was effectively used for opening cyclic ethers to produce alpha -iodo- and bromoalkanols. The synthesis of 4-iodobutanoic acid from gamma -butyrolactone has also been described. The method is based on the use of a dried Dowex H super(+)/NaX (X = Br, I)-system, which is effective at producing alpha -iodoalkanols and some alpha -bromoalkanols from commercially available cyclic ethers. Additionally, opening of three different crown ethers to form alpha -iodo(polyethylene)glycols with various chain lengths is demonstrated. Haloalkanols are important building blocks in synthetic chemistry e.g. for medicinal chemistry purposes.</description><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c5ra20813k</identifier><language>eng</language><subject>Chains ; Crown ethers ; Ethers ; Synthesis</subject><ispartof>RSC advances, 2016-02, Vol.6 (19), p.15937-15940</ispartof><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></links><search><creatorcontrib>Turhanen, Petri A</creatorcontrib><creatorcontrib>Vepsaelaeinen, Jouko J</creatorcontrib><title>Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach</title><title>RSC advances</title><description>Our recently reported novel green chemistry tool was effectively used for opening cyclic ethers to produce alpha -iodo- and bromoalkanols. The synthesis of 4-iodobutanoic acid from gamma -butyrolactone has also been described. The method is based on the use of a dried Dowex H super(+)/NaX (X = Br, I)-system, which is effective at producing alpha -iodoalkanols and some alpha -bromoalkanols from commercially available cyclic ethers. Additionally, opening of three different crown ethers to form alpha -iodo(polyethylene)glycols with various chain lengths is demonstrated. Haloalkanols are important building blocks in synthetic chemistry e.g. for medicinal chemistry purposes.</description><subject>Chains</subject><subject>Crown ethers</subject><subject>Ethers</subject><subject>Synthesis</subject><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqVT8tOwzAQtJCQqKAXvmCPqWiondCoPXDhpXJBPfTQW7VxHGLieoM3FvAPfDRG4geYy8xoZlcaIS6VvFayXC_0MmAhV6rsT8SkkDdVXshqfSamzG8yoVqqolIT8b0NZsCAoyUP1EJk00YHdbSusf4Vake65zmgGzqE3FJDOaBvoA50JHQ9enIMbXKgv7SzGszYmcDp0-990vBAH-YTNsBxMCG7mi1ecA_ZHm7heQ53YQY4DIFQdxfitEXHZvrH5yJ7etzdb_IUv0fD4-FoWRvn0BuKfFArmZalNar8R_UHZ0JanQ</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Turhanen, Petri A</creator><creator>Vepsaelaeinen, Jouko J</creator><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20160201</creationdate><title>Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach</title><author>Turhanen, Petri A ; Vepsaelaeinen, Jouko J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_18004600013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chains</topic><topic>Crown ethers</topic><topic>Ethers</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Turhanen, Petri A</creatorcontrib><creatorcontrib>Vepsaelaeinen, Jouko J</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Turhanen, Petri A</au><au>Vepsaelaeinen, Jouko J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach</atitle><jtitle>RSC advances</jtitle><date>2016-02-01</date><risdate>2016</risdate><volume>6</volume><issue>19</issue><spage>15937</spage><epage>15940</epage><pages>15937-15940</pages><eissn>2046-2069</eissn><abstract>Our recently reported novel green chemistry tool was effectively used for opening cyclic ethers to produce alpha -iodo- and bromoalkanols. The synthesis of 4-iodobutanoic acid from gamma -butyrolactone has also been described. The method is based on the use of a dried Dowex H super(+)/NaX (X = Br, I)-system, which is effective at producing alpha -iodoalkanols and some alpha -bromoalkanols from commercially available cyclic ethers. Additionally, opening of three different crown ethers to form alpha -iodo(polyethylene)glycols with various chain lengths is demonstrated. Haloalkanols are important building blocks in synthetic chemistry e.g. for medicinal chemistry purposes.</abstract><doi>10.1039/c5ra20813k</doi></addata></record> |
fulltext | fulltext |
identifier | EISSN: 2046-2069 |
ispartof | RSC advances, 2016-02, Vol.6 (19), p.15937-15940 |
issn | 2046-2069 |
language | eng |
recordid | cdi_proquest_miscellaneous_1800460001 |
source | Royal Society Of Chemistry Journals |
subjects | Chains Crown ethers Ethers Synthesis |
title | Preparation of useful building blocks, alpha -iodo- and bromoalkanols from cyclic ethers using the Dowex H super(+)/NaX (X = I, Br) approach |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T23%3A18%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preparation%20of%20useful%20building%20blocks,%20alpha%20-iodo-%20and%20bromoalkanols%20from%20cyclic%20ethers%20using%20the%20Dowex%20H%20super(+)/NaX%20(X%20=%20I,%20Br)%20approach&rft.jtitle=RSC%20advances&rft.au=Turhanen,%20Petri%20A&rft.date=2016-02-01&rft.volume=6&rft.issue=19&rft.spage=15937&rft.epage=15940&rft.pages=15937-15940&rft.eissn=2046-2069&rft_id=info:doi/10.1039/c5ra20813k&rft_dat=%3Cproquest%3E1800460001%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1800460001&rft_id=info:pmid/&rfr_iscdi=true |