HPLC Resolution of Hydroxyl Carboxylic Acid Enantiomers Using 2-Quinoxaloyl Chloride as a New Precolumn Derivatizing Agent
Chiral α-hydroxy carboxylic acids were reacted using 2-quinoxaloyl chloride to form UV and fluorescent derivatives. Under mild conditions either in aqueous or non-aqueous conditions reaction proceeds quickly and without racemisation. The labelled compounds have been resolved into enantiomers on β-cy...
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Veröffentlicht in: | Journal of liquid chromatography 1995-08, Vol.18 (14), p.2765-2781 |
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container_title | Journal of liquid chromatography |
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creator | Brightwell, Malcolm Pawlowska, Maria Zukowski, Janusz |
description | Chiral α-hydroxy carboxylic acids were reacted using 2-quinoxaloyl chloride to form UV and fluorescent derivatives. Under mild conditions either in aqueous or non-aqueous conditions reaction proceeds quickly and without racemisation. The labelled compounds have been resolved into enantiomers on β-cyclodextrin bonded stationary phase operated with polar organic eluents. The high sensitivity and selectivity of the method has been used for the determination of low levels of enantiomeric impurities in commercial "pure" samples. |
doi_str_mv | 10.1080/10826079508009323 |
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Under mild conditions either in aqueous or non-aqueous conditions reaction proceeds quickly and without racemisation. The labelled compounds have been resolved into enantiomers on β-cyclodextrin bonded stationary phase operated with polar organic eluents. 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Under mild conditions either in aqueous or non-aqueous conditions reaction proceeds quickly and without racemisation. The labelled compounds have been resolved into enantiomers on β-cyclodextrin bonded stationary phase operated with polar organic eluents. The high sensitivity and selectivity of the method has been used for the determination of low levels of enantiomeric impurities in commercial "pure" samples.</description><subject>Analytical chemistry</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Exact sciences and technology</subject><subject>Other chromatographic methods</subject><issn>0148-3919</issn><issn>2331-0413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUhoMoWGofwF0WbkdzmUsDbkqtVihaxa6HM5mkRqZJSaa206c3pepGPItz4__OgR-hS0quKRmSm5hYTgqRxYEIzvgJ6jHOaUJSyk9Rj9B0mHBBxTkahPBBYmRpkebDHtpP57MxflXBNZvWOIudxtOu9m7XNXgMvjo0RuKRNDWeWLBRtFI-4EUwdolZ8rIx1u2gcQf9e-O8qRWGgAE_qS2eeyXj5ZXFd8qbT2jN_oCNlsq2F-hMQxPU4Lv20eJ-8jaeJrPnh8fxaJZIzrI2yZXQOVOplnXNNUgqdZVTpYQUVLOiyHihGVQig2gCVBXVgseVJlpTXRHO-4ge70rvQvBKl2tvVuC7kpLy4F_5x7_IXB2ZNQQJjfZgpQm_IM85Z8Uwym6PMmO18yvYOt_UZQtd9OGH4f9_-QJWG4RD</recordid><startdate>19950801</startdate><enddate>19950801</enddate><creator>Brightwell, Malcolm</creator><creator>Pawlowska, Maria</creator><creator>Zukowski, Janusz</creator><general>Taylor & Francis Group</general><general>Dekker</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19950801</creationdate><title>HPLC Resolution of Hydroxyl Carboxylic Acid Enantiomers Using 2-Quinoxaloyl Chloride as a New Precolumn Derivatizing Agent</title><author>Brightwell, Malcolm ; Pawlowska, Maria ; Zukowski, Janusz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-6e9f62e4fcdd3fac1cfb61ee9c91f277537f2ab95a826abb1f9337ff0ff1fb033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Analytical chemistry</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Exact sciences and technology</topic><topic>Other chromatographic methods</topic><toplevel>online_resources</toplevel><creatorcontrib>Brightwell, Malcolm</creatorcontrib><creatorcontrib>Pawlowska, Maria</creatorcontrib><creatorcontrib>Zukowski, Janusz</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of liquid chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brightwell, Malcolm</au><au>Pawlowska, Maria</au><au>Zukowski, Janusz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HPLC Resolution of Hydroxyl Carboxylic Acid Enantiomers Using 2-Quinoxaloyl Chloride as a New Precolumn Derivatizing Agent</atitle><jtitle>Journal of liquid chromatography</jtitle><date>1995-08-01</date><risdate>1995</risdate><volume>18</volume><issue>14</issue><spage>2765</spage><epage>2781</epage><pages>2765-2781</pages><issn>0148-3919</issn><eissn>2331-0413</eissn><coden>JLCHD8</coden><abstract>Chiral α-hydroxy carboxylic acids were reacted using 2-quinoxaloyl chloride to form UV and fluorescent derivatives. Under mild conditions either in aqueous or non-aqueous conditions reaction proceeds quickly and without racemisation. The labelled compounds have been resolved into enantiomers on β-cyclodextrin bonded stationary phase operated with polar organic eluents. The high sensitivity and selectivity of the method has been used for the determination of low levels of enantiomeric impurities in commercial "pure" samples.</abstract><cop>New York, NY</cop><pub>Taylor & Francis Group</pub><doi>10.1080/10826079508009323</doi><tpages>17</tpages></addata></record> |
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source | Taylor & Francis:Master (3349 titles) |
subjects | Analytical chemistry Chemistry Chromatographic methods and physical methods associated with chromatography Exact sciences and technology Other chromatographic methods |
title | HPLC Resolution of Hydroxyl Carboxylic Acid Enantiomers Using 2-Quinoxaloyl Chloride as a New Precolumn Derivatizing Agent |
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