首页> 外文期刊>Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry >High‐performance liquid chromatographic enantioseparation of NN ‐aryl‐thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide‐based chiral stationary phases
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High‐performance liquid chromatographic enantioseparation of NN ‐aryl‐thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide‐based chiral stationary phases

机译: n-in-in-inhiouroido烷基膦酸盐和硫胺(烷基膦酸盐)对基于多糖的手性静脉阶段的高性能液相色谱映像分析

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Abstract > The first successful enantioseparation of representative <fi>O,O</fi> ‐diphenyl‐ <fi>N</fi> ‐arylthioureidoalkylphosphonates, (±)‐Ptc‐Val P (OPh) <sub>2</sub> & (±)‐Ptc‐Leu P (OPh) <sub>2</sub> and thiourylenedi(isobutyl phosphonate), Tcm[Val P (OPh) <sub>2</sub> ] <sub>2</sub> on analytical and semipreparative scale was achieved by high‐performance liquid chromatography using polysaccharide‐based chiral stationary phases (CPs). Atc‐AA P (OPh) <sub>2</sub> was obtained using modified tricomponent condensations of the corresponding aldehydes, <fi>N</fi> ‐arylthiourea and triphenyl phosphite whereas Tcm[Val P (OPh) <sub>2</sub> ] <sub>2</sub> by the condensations of aldehydes, thiourea, and triphenyl phosphite. The prepared, racemic (±)‐Atc‐AA P (OPh) <sub>2</sub> [(±)‐Ptc‐Val P (OPh) <sub>2</sub> , (±)‐Ptc‐Leu P (OPh) <sub>2</sub> , (±)‐Ptc‐Pgly P (OPh) <sub>2</sub> and (±)‐Ntc‐Pgly P (OPh) <sub>2</sub> ] and racemic (±)‐Tcm[AA P (OPh) <sub>2</sub> ] <sub>2</sub> [(±)‐Tcm[Nva P (OPh) <sub>2</sub> ] <sub>2</sub> & (±)‐Tcm[Val P (OPh) <sub>2</sub> ] <sub>2</sub> ] were adequately characte </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> <div class="translation abstracttxt"> <span class="zhankaihshouqi fivelineshidden" id="abstract"> <span>机译:</span><Abstract Type =“Main”XML:Lang =“en”> <标题类型=“main”>抽象</ title> >代表的第一个成功的阐述<fi> o,o </ fi> -diphenyl- <fi> n </ fi> - 硫代萘烷基膦酸盐,(±)-ptc-val p </ sup>(OPH)<sub> 2 </ sub>&amp; (±)-ptC-Leu p </ sup>(OPH)<sub> 2 </ sub>和硫硝丁烯(异丁基膦酸盐),tcm [val p </ sup>(oph)<sub>通过使用基于多糖的手性固定阶段(CPS)的高性能液相色谱法实现了分析和半乙醛的2 </ sub>] <sub> 2 </ sub>。使用相应的醛的改性的三分组分缩合获得ATC-AA p </ sup>(OPH)<sub> 2 </ sub>,<fi> n </ fi> - 亚芳硫脲和三苯基亚磷矿,而TCM [val通过醛,硫脲和三苯基亚磷矿的缩合来 p </ sup>(OPH)<sub> 2 </ sub>] <sub> 2 </ sub>。制备的外消旋(±)-ATC-AA p </ sup>(OPH)<sub> 2 </ sub> [(±)-ptc-val p </ sup>(oph)< Sub> 2 </ sub>,(±)-ptc-Leu p </ sup>(OPH)<sub> 2 </ sub>,(±)-ptc-pgly p </ sup> (OPH)<sub> 2 </ sub>和(±)-ntc-pgly p </ sup>(OPH)<sub> 2 </ sub>]和外消旋(±)-tcm [aa <sup > P </ sup>(OPH)<sub> 2 </ sub>] <sub> 2 </ sub> [(±)-tcm [nva p </ sup>(oph)<sub> 2 < / sub>] <sub> 2 </ sub>&amp; (±)-tcm [val p </ sup>(OPH)<sub> 2 </ sub>] <sub> 2 </ sub>]是充分的characte </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> </div> <div class="record"> <h2 class="all_title" id="enpatent33" >著录项</h2> <ul> <li> <span class="lefttit">来源</span> <div style="width: 86%;vertical-align: text-top;display: inline-block;"> <a href='/journal-foreign-16290/'>《Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry》</a> <b style="margin: 0 2px;">|</b><span>2018年第2期</span><b style="margin: 0 2px;">|</b><span>共10页</span> </div> </li> <li> <div class="author"> <span class="lefttit">作者</span> <p id="fAuthorthree" class="threelineshidden zhankaihshouqi"> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Drabowicz Józef&option=202" target="_blank" rel="nofollow">Drabowicz Józef;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kudzin Marcin H.&option=202" target="_blank" rel="nofollow">Kudzin Marcin H.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kudzin Zbigniew H.&option=202" target="_blank" rel="nofollow">Kudzin Zbigniew H.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Pokora‐Sobczak Patrycja&option=202" target="_blank" rel="nofollow">Pokora‐Sobczak Patrycja;</a> </p> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zkzz" style="display: none;">展开▼</span> </div> </li> <li> <div style="display: flex;"> <span class="lefttit">作者单位</span> <div style="position: relative;margin-left: 3px;max-width: 639px;"> <div class="threelineshidden zhankaihshouqi" id="fOrgthree"> <p>Centre of Molecular and Macromolecular StudiesPolish Academy of SciencesWarsaw Poland;</p> <p>Textile Research InstituteLodz Poland;</p> <p>Faculty of ChemistryUniversity of LodzLodz Poland;</p> <p>Centre of Molecular and Macromolecular StudiesPolish Academy of SciencesWarsaw Poland;</p> </div> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zhdw" style="display: none;">展开▼</span> </div> </div> </li> <li > <span class="lefttit">收录信息</span> <span style="width: 86%;vertical-align: text-top;display: inline-block;"></span> </li> <li> <span class="lefttit">原文格式</span> <span>PDF</span> </li> <li> <span class="lefttit">正文语种</span> <span>eng</span> </li> <li> <span class="lefttit">中图分类</span> <span><a href="https://www.zhangqiaokeyan.com/clc/4812.html" title="结构化学">结构化学;</a></span> </li> <li class="antistop"> <span class="lefttit">关键词</span> <p style="width: 86%;vertical-align: text-top;"> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=chiral HPLC&option=203" rel="nofollow">chiral HPLC;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=enantiomers&option=203" rel="nofollow">enantiomers;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=meso compounds&option=203" rel="nofollow">meso compounds;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=N ‐arylthioureidoalkylphosphonates&option=203" rel="nofollow">N ‐arylthioureidoalkylphosphonates;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=thioureas&option=203" rel="nofollow">thioureas;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=thiourylenedi(alkylphosphonates)&option=203" rel="nofollow">thiourylenedi(alkylphosphonates);</a> </p> <div class="translation"> 机译:手性HPLC;对映异构体;中索化合物;N-芳硫代烷烷基膦酸盐;硫酸;硫酸丁苯(烷基膦酸盐); </div> </li> </ul> </div> </div> <div class="literature cardcommon"> <div class="similarity "> <h3 class="all_title" id="enpatent66">相似文献</h3> <div class="similaritytab clearfix"> <ul> <li class="active" >外文文献</li> <li >中文文献</li> <li >专利</li> </ul> </div> <div class="similarity_details"> <ul > <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/0704022113452.html">High‐performance liquid chromatographic enantioseparation of <fi >N</fi>N ‐aryl‐thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide‐based chiral stationary phases</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Drabowicz Józef&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Drabowicz Józef,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kudzin Marcin H.&option=202" target="_blank" rel="nofollow" class="tuijian_auth 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<span>-1</span> </span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:在新开发的异丙基氨基甲酸酯-ConcOfructan6(IP-CF6)手性固定阶段的高效液相色谱映像对β基碱基酶进行分析</span> </p> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/open-access_resources_thesis/0100016719754.html ">High-performance liquid chromatographic enantioseparation of unusual amino acid derivatives with axial chirality on polysaccharide-based chiral stationary phases</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=López-Ram-de-Víu, Pilar&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">López-Ram-de-Víu, Pilar,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Gálvez, José A.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Gálvez, José A.,</a> <a 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Chun&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . Li Chun</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李春&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,李春</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Li Weixun&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,Li Weixun</a> <span> <a href="/conference-cn-6670/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 第十七届全国金属有机化学学术讨论会 </a> <span> <span> . 2012</span> </span> </div> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/academic-degree-domestic_mphd_thesis/020313129416.html">新型含膦β-二亚胺稀土金属配合物的合成及其在氢胺烷基化反应中的应用</a> <b>[A] </b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=高红杰&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 高红杰</a> <span> . 2018</span> </span> </div> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/06120109322.html">在三烷基胺或三烷基膦存在下对烷基或苄基氰衍生物烷基化的方法</a> <b>[P]</b> . <span> 中国专利: CN1119322C </span> <span> . 2003.08.27</span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/06120104425556.html">在三烷基胺或三烷基膦存在下对烷基或苄基氰衍生物烷基化的方法</a> <b>[P]</b> . <span> 中国专利: CN1222505A </span> <span> . 1999-07-14</span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130443849312.html">LC Liquid chromatographic ligand exchange chiral stationary phases chiral columns packed with the ligand exchange chiral stationary phases</a> <b>[P]</b> . <span> 外国专利: <!-- 韩国专利: --> KR20030077238A </span> <span> . 2003-10-01</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:LC液相色谱配体交换手性固定相填充有配体交换手性固定相的手性柱 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130439216655.html">LIQUID CHROMATOGRAPHIC CHIRAL CROWN ETHER-BASED STATIONARY PHASES WITH NOVEL DOUBLE TETHERING GROUPS AND THE CHIRAL COLUMNS</a> <b>[P]</b> . <span> 外国专利: <!-- 韩国专利: --> KR100516972B1 </span> <span> . 2005-09-26</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:液相色谱手性冠基于醚的固定相,具有两个双配位基团和手性柱 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130441595305.html">LIQUID CHROMATOGRAPHIC CHIRAL CROWN ETHER-BASED STATIONARY PHASES WITH NOVEL DOUBLE TETHERING GROUPS AND THE CHIRAL COLUMNS PACKED WITH THE SAME</a> <b>[P]</b> . <span> 外国专利: <!-- 韩国专利: --> KR20040090244A </span> <span> . 2004-10-22</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:液相色谱手性冠基于醚的固定相,具有两个双配位基团,并且手性柱具有相同的包装 </span> </p> </li> </ul> </div> </div> </div> <div class="theme cardcommon" style="overflow: auto;display:none"> <h3 class="all_title" id="enpatent55">相关主题</h3> <ul id="subject"> </ul> </div> </div> </div> </div> <div class="right rightcon"> <div class="details_img cardcommon clearfix" style="margin-bottom: 10px;display:none;" > </div> </div> </div> <div id="thesis_get_original1" class="downloadBth" style="bottom: 19px;z-index: 999;" onclick="ywcd('0704022113452','4',7,2,1,'',this,24)" class="delivery" prompt="010401" title="通过人工服务将文献原文发送至邮箱" >获取原文</div> <div class="journalsub-pop-up" style="display: none"> <div class="journal-sub"> <h2>期刊订阅</h2> <img src="https://cdn.zhangqiaokeyan.com/img/loginclose.png" alt="" onclick="$('.journalsub-pop-up').hide()"> <p class="pardon">抱歉,该期刊暂不可订阅,敬请期待!</p> <p class="current">目前支持订阅全部北京大学中文核心(2020)期刊目录。</p> <div style="display: flex;margin-top: 69px;justify-content: space-between;"> <div class="no-sub" 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