• 主题
高级搜索  >
历史搜索 清空历史
首页> 外文期刊>Journal of Physical Organic Chemistry >Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ 9H9H ‐thioxanthenium hexafluorophosphates and 2,4‐dimethyl(diethyl)‐ 9H9H ‐thioxanthene‐9‐ones
【24h】

Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ 9H9H ‐thioxanthenium hexafluorophosphates and 2,4‐dimethyl(diethyl)‐ 9H9H ‐thioxanthene‐9‐ones

机译：2,4-二甲基（二乙基）-9-氧代-10-（4-庚氧基苯基） - 9H六氟磷酸盐和2,4-二甲基（二乙基） - 9h的电化学还原 9h-硫氧蒽-9-

获取原文
获取原文并翻译 | 示例
       
页面导航
  • 摘要
  • 著录项
  • 相似文献
  • 相关主题

摘要

Abstract > Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ <fi>9H</fi> ‐thioxanthenium hexafluorophosphates in acetonitrile (MeCN) and <fi>N</fi> , <fi>N</fi> ‐dimethylformamide is an irreversible 1‐electron process accompanied by the cleavage of the C(Ph)‐S bond in thioxanthenium cations with the formation of the corresponding 2,4‐dimethyl(diethyl)‐ <fi>9H</fi> ‐thioxanthene‐9‐ones. One‐electron reversible electrochemical reduction of the latter compounds occurs at more negative potentials and yields the corresponding radical anions, which have been characterized by electron paramagnetic resonance spectroscopy and density functional theory calculations at the (U)B3LYP/6‐31+G*/polarizable continuum model level of theory. </abstract> </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”>摘要</标题> >电化学还原2,4-二甲基（二乙基）-9-氧代-10-（ 4-庚氧基苯基） - <FI> 9H </ FI> - 乙腈（MECN）和<FI> N </ FI>中的六氟磷酸盐，<FI> N </ FI> - 二甲基甲酰胺是一种不可逆的1-Electron方法 用相应的2,4-二甲基（二乙基） - <Fi> 9H </ Fi> - 硫铵-9-甲氧吡啶阳离子C（pH）-S -s -s键的切割。 后两种化合物的一种电子可逆电化学减少在更负电势下发生并产生相应的自由基阴离子，其特征在于（U）B3LYP / 6-31 + G * /密度函数理论计算。 极化连续模型理论水平。 </ p> </ abstract> </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-35546/'>《Journal of Physical Organic Chemistry》</a> <b style="margin: 0 2px;">|</b><span>2018年第9期</span><b style="margin: 0 2px;">|</b><span>共7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=Shundrin Leonid A.&option=202" target="_blank" rel="nofollow">Shundrin Leonid A.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Avrorov Pavel A.&option=202" target="_blank" rel="nofollow">Avrorov Pavel A.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Irtegova Irina G.&option=202" target="_blank" rel="nofollow">Irtegova Irina G.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Odintsov Danila S.&option=202" target="_blank" rel="nofollow">Odintsov Danila S.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Poveshchenko Alexander F.&option=202" target="_blank" rel="nofollow">Poveshchenko Alexander F.;</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>N. N. Vorozhtsov Institute of Organic ChemistryRussian Academy of SciencesNovosibirsk Russia;</p> <p>N. N. Vorozhtsov Institute of Organic ChemistryRussian Academy of SciencesNovosibirsk Russia;</p> <p>N. N. Vorozhtsov Institute of Organic ChemistryRussian Academy of SciencesNovosibirsk Russia;</p> <p>N. N. Vorozhtsov Institute of Organic ChemistryRussian Academy of SciencesNovosibirsk Russia;</p> <p>The Scientific Institute of Clinical and Experimental LymphologyRussian Academy of Medical SciencesNovosibirsk Russia;</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/4796.html" title="有机化学一般性问题">有机化学一般性问题;</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=cyclic voltammetry&option=203" rel="nofollow">cyclic voltammetry;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=DFT calculations&option=203" rel="nofollow">DFT calculations;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=EPR spectroscopy&option=203" rel="nofollow">EPR spectroscopy;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=radical anions&option=203" rel="nofollow">radical anions;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=thioxanthenium salts&option=203" rel="nofollow">thioxanthenium salts;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=thioxanthenones&option=203" rel="nofollow">thioxanthenones;</a> </p> <div class="translation"> 机译：循环伏安;DFT计算;epr光谱;自由基阴离子;硫代噻吩;硫代噻吩; </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/0704025793861.html">Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ <i >9H9H ‐thioxanthenium hexafluorophosphates and 2,4‐dimethyl(diethyl)‐ <i >9H9H ‐thioxanthene‐9‐ones</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Shundrin Leonid A.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Shundrin Leonid A.,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Avrorov Pavel A.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Avrorov Pavel A.,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Irtegova Irina G.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Irtegova Irina G.,</a> <a href="/journal-foreign-35546/" target="_blank" rel="nofollow" class="tuijian_authcolor">Journal of Physical Organic Chemistry .</a> <span>2018</span><span>,第9期</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：2,4-二甲基（二乙基）-9-氧代-10-（4-庚氧基苯基） - <I> 9H六氟磷酸盐和2,4-二甲基（二乙基） - 9h的电化学还原 </ i> 9h-硫氧蒽-9-</span> </p> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/070408462193.html">Synthesis of Hexafluorophosphates of 9-Oxo-10-(4-heptoxyphenyl)thioxanthenium</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=V.A.Loskutov&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">V.A.Loskutov,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=V.B.Shelkovnikov&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">V.B.Shelkovnikov </a> <a href="/journal-foreign-27442/" target="_blank" rel="nofollow" class="tuijian_authcolor">Russian Journal of Organic Chemistry .</a> <span>2006</span><span>,第2期</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：9-氧代-10-（4-庚氧基苯基）噻吨六氟磷酸盐的合成</span> </p> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-foreign_detail_thesis/0204118471154.html">Dimethyl 3,5-diethyl-1H-pyrrole-2,4-dicarboxyl­ate</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lin W.-S.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Lin W.-S.,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lu G.-F.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Lu G.-F.,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Ou Z.-P.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Ou Z.-P.,</a> <a href="/journal-foreign-17695/" target="_blank" rel="nofollow" class="tuijian_authcolor">Acta Crystallographica Section E: Crystallographic Communications .</a> <span>2011</span><span>,第8期</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：3,5-二乙基-1H-吡咯-2,4-二羧酸二甲酯</span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-conference-foreign_meeting-251184_thesis/070508709341.html">Catalytic Synthesis of Dimethyltoluene-2,4-dicarbamate by the Methoxycarbonylation of 2,4-Toluene Diamine with Dimethyl Carbonate Using Zn (OAc)_2·2H_2O</a> <b>[C]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Toshihide Baba&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Toshihide Baba,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Akane Kobayashi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Akane Kobayashi,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Tatsuya Yamauchi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Tatsuya Yamauchi,</a> <a href="/conference-foreign-251184/" target="_blank" rel="nofollow" class="tuijian_authcolor">Tokyo Conference on Advanced Catalytic Science and Technology .</a> <span>2003</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：用Zn（OAC）二甲基碳酸二甲酯甲氧基羰基化催化合成二甲基甲苯-2,4-二氨基甲酸甲酸甲氧基羰基化_2·2H_2O</span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-degree-foreign_mphd_thesis/02061891466.html">Effects of Nitrite, Nitrate, and Humic Acid on the Photodegradation of Dimethyl, Diethyl, and Dipropyl Phthalic Acid Ester</a> <b>[D] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=?Lu, Xiaofei&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">?Lu, Xiaofei </a> <span>2020</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：亚硝酸盐，硝酸盐和腐殖酸对二甲基，二乙基和双苯二甲酸酯的光降解的影响</span> </p> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-journal-foreign-pmc_detail_thesis/040004312915.html">(Z)-3-Diethyl­amino-6-({2-(E)-4-(diethyl­amino)-2-hy­droxy­benzyl­idene­amino-45-dimethyl­phen­yl}amino­methyl­idene)cyclo­hexa-24-dienone–55′-bis­(diethyl­amino)-22′-45-dimethyl-o-phenyl­enebis(nitrilo­methyl­idyne)diphenol</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Hadi Kargar&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Hadi Kargar,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Reza Kia&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Reza Kia,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Muhammad Nawaz Tahir&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Muhammad Nawaz Tahir </a> <span>2010</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：（Z）-3-二乙氨基-6-（{2-（（E）-4-（二乙氨基）-2-羟基苄叉亚氨基 -45-二甲基苯基}氨基亚甲基）环己-24-二烯酮–55 -双（二乙氨基）-22-45-二甲基-邻苯撑双（亚硝基甲基二炔）二酚</span> </p> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/open-access_resources_thesis/0100037649396.html ">(Z)-3-Diethyl­amino-6-({2-[(E)-4-(diethyl­amino)-2-hy­droxy­benzyl­idene­amino]-4,5-dimethyl­phen­yl}amino­methyl­idene)cyclo­hexa-2,4-dienone–5,5′-bis­(diethyl­amino)-2,2′-[4,5-dimethyl-o-phenyl­enebis(nitrilo­methyl­idyne)]diphenol</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kargar, Hadi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Kargar, Hadi,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kia, Reza&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Kia, Reza,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Tahir, Muhammad Nawaz&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Tahir, Muhammad Nawaz </a> <span>2010</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：（Z）-3-二乙基氨基-6-（{2-[（E）-4-（二乙基氨基）-2-羟基苄叉亚氨基] -4,5-二甲基苯基}氨基亚甲基）环己-2,4-二烯酮–5,5' -双（二乙氨基）-2,2'-[4,5-二甲基-邻苯撑双（亚硝基甲基二炔）]二酚</span> </p> </li> <li> <div> <b>8. </b><a class="enjiyixqcontent" href="/ntis-science-report_de_thesis/02071452818.html">Initial Submission: Subacute Dog Study of 3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro (4.5)-3-en-4-yl Ester, 2,2-dimethyl-butano*, W/tsca Health & Safety Study Cover Sheet dated 061699.</a> <b>[R] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> </a> <span>1999</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：初始提交：亚急性狗研究3-（2,4-二氯苯基）-2-氧代-1-氧杂螺（4.5）-3-烯-4-基酯，2,2-二甲基丁醇*，W / tsca健康和安全研究封面表日期为061699。</span> </p> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-structural-chemistry_thesis/0201235838421.html">3,6-二甲基-9-对硝基苯基-1,8-二氧代-2,7,10-三氧杂蒽的合成和晶体结构</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=高原&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 高原</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘剑洪&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,刘剑洪</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=黄毅&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,黄毅</a> <span> <a href="/journal-cn-12157/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 结构化学 </a> </span> <span> . 2004</span><span>,第005期</span> </span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-cn_detail_thesis/0201293853878.html">3，3－二甲基－7，11－二苯基螺［5，5］－2，4－二氧杂十一烷－1，5，9－三酮的合成</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=卢淑和&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 卢淑和</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=陈洪超&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,陈洪超</a> <span> <a href="/journal-cn-57016/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 华西药学杂志 </a> </span> <span> . 1995</span><span>,第1期</span> </span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-structural-chemistry_thesis/0201235837371.html">3,3,6,6-四甲基-9-(3,4-亚甲二氧基苯基)-1,8-二氧代-2,3,4,5,6,7-六氢夹氧蒽的合成和晶体结构</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=屠树江&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 屠树江</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=缪春宝&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,缪春宝</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=房芳&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,房芳</a> <span> <a href="/journal-cn-12157/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 结构化学 </a> </span> <span> . 2004</span><span>,第002期</span> </span> </div> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-tianjin-normal-university-natural-science-edition_thesis/0201250797888.html">1,10-邻菲啰啉与4,5-双二苯基膦-9,9-二甲基氧杂蒽混合配位铜(Ⅰ)的合成与表征</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=王斌&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 王斌</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=韩贤柱&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,韩贤柱</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘鲲&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,刘鲲</a> <span> <a href="/journal-cn-4723/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 天津师范大学学报（自然科学版） </a> </span> <span> . 2014</span><span>,第003期</span> </span> </div> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-structural-chemistry_thesis/0201273658620.html">3,3—二甲基—9-(5,5—二甲基—3—羟基—2—环己烯—1—酮—2—基)—1—氧代—2,3,4,9—四氢化氧杂蒽的合成和晶体结构</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=史达清&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 史达清</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=路再生&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,路再生</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=戴桂元&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,戴桂元</a> <span> <a href="/journal-cn-12157/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 结构化学 </a> </span> <span> . 1998</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-conference-cn_meeting-4306_thesis/020221032424.html">Cu-OMS-2催化{(3R,4R)-3-(1'R)-叔丁基二甲基硅氧乙基-4-乙羧基-1-对甲氧基苯基-2-氮杂环丁酮}脱羧乙酰氧基化的研究</a> <b>[C]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=周军荣&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 周军荣</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=曹佳&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,曹佳</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=钱广&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,钱广</a> <span> <a href="/conference-cn-4306/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 第十届全国工业催化技术及应用年会 </a> <span> <span> . 2013</span> </span> </div> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/academic-degree-domestic_mphd_thesis/02031754185.html">硫杂蒽-9-硫酮及9-(1-苯基乙基)-9-(甲硫基)-9H-氧杂蒽调节MMA/St可控自由基聚合探究</a> <b>[A] </b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=闫润&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 闫润</a> <span> . 2017</span> </span> </div> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/061201421891.html">N-[2-(二乙基氨基)乙基]-5-[(5-氟-1,2-二氢-2-氧代-3H-吲哚-3-亚基)甲基]-2,4-二甲基-1H-吡咯-3-甲酰胺的晶型及其制备方法</a> <b>[P]</b> . <span> 中国专利： CN101965342B </span> <span> . 2014.07.30</span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/06120106158481.html">N-2-(二乙基氨基)乙基-5-(5-氟-1,2-二氢-2-氧代-3H-吲哚-3-亚基)甲基-2,4-二甲基-1H-吡咯-3-甲酰胺的晶型及其制备方法</a> <b>[P]</b> . <span> 中国专利： CN101965342A </span> <span> . 2011-02-02</span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130461466027.html">METHOD OF SYNTHESIS OF N-(1-METHOXYPROP-2-YL)-2,4-DIMETHYL-3-AMINOTHIOPHENE, 2,4-DIMETHYL-2,3-DIHYDROTHIOPHENE-3-ONE AS AN INTERMEDIATE PRODUCT FOR SYNTHESIS OF N-(1-METHOXYPROP-2-YL)-2,4-DIMETHYL-3-AMINOTHIOPHENE, AND DERIVATIVES OF 2,4-DIMETHYL-2,3-DIHYDROTHIOPHENE-3-ONE AS PARENT PRODUCTS FOR SYNTHESIS</a> <b>[P]</b> . <span> 外国专利： <!-- 俄罗斯专利： --> RU1819266C </span> <span> . 1993-05-30</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：N-（1-甲氧基丙-2-基）-2,4-二甲基-3-酰胺基噻吩，2,4-二甲基-2,3-二氢噻吩-3-酮的合成中间体（1-甲氧基丙-2-基）-2,4-二甲基-3-酰胺基噻吩和2,4-二甲基-2,3-二氢噻吩-3-酮的衍生物作为合成的母体 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130461423136.html">METHOD OF SYNTHESIS OF N-(1-METHOXYPROP-2-YL)-2,4-DIMETHYL-3-AMINOTHIOPHENE, 2,4-DIMETHYL-2,3-DIHYDROTHIOPHENE-3-ONE AS AN INTERMEDIATE PRODUCT FOR SYNTHESIS OF N-(1-METHOXYPROP-2-YL)-2,4-DIMETHYL-3-AMINOTHIOPHENE, AND DERIVATIVES OF 2,4-DIMETHYL-2,3-DIHYDROTHIOPHENE-3-ONE AS PARENT PRODUCTS FOR SYNTHESIS</a> <b>[P]</b> . <span> 外国专利： <!-- --> SU01819266A3 </span> <span> . 1993-05-30</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：N-（1-甲氧基丙-2-基）-2,4-二甲基-3-酰胺基噻吩，2,4-二甲基-2,3-二氢噻吩-3-酮的合成中间体（1-甲氧基丙-2-基）-2,4-二甲基-3-酰胺基噻吩和2,4-二甲基-2,3-二氢噻吩-3-酮的衍生物作为合成的母体 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130402562628.html">HERBICIDAL MIXTURES CONTAINING 2-2,4-DICHLOROPHENYL)METHYL4,4-DIMETHYL-3-ISOXAZOLIDINONE, PYROXASULFONE AND MEFENPYR-DIETHYL</a> <b>[P]</b> . <span> 外国专利： <!-- 欧洲知识产权局专利： --> EP3599856A1 </span> <span> . 2020-02-05</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：包含2- [2,4-二氯苯基]甲基] 4,4-二甲基-3-异恶唑烷酮，吡咯烷酮和甲萘啶二酮的除草剂混合物 </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('0704025793861','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="$('.journalsub-pop-up').hide()"> <p class="pardon">抱歉，该期刊暂不可订阅，敬请期待！</p> <p class="current">目前支持订阅全部北京大学中文核心（2020）期刊目录。</p> <div style="display: flex;margin-top: 69px;justify-content: space-between;"> <div class="no-sub" onclick="$('.journalsub-pop-up').hide()">暂不订阅</div> <div class="other-sub" onclick="continueSub('from=pc-detail')">继续订阅其他期刊</div> </div> </div> </div> <div class="right_btn"> <ul> <li class="gouwuche"> <!-- <a href="javascript:void(0);" onclick="link_analysis('/shoppingcart/auth/list.html',this)">购物车</a>--> </li> <li class="yijian"> <a href="javascript:void(0);" onclick="link_analysis('/mycenter/auth/complaint.html',this)">意见反馈</a> </li> <li class="top"> <a href="javascript:scrollTo(0,0);">回到顶部</a> </li> <li class="shouye"> <a href="/">回到首页</a> </li> </ul> </div> <div class="xllindexfooter"> <div class="xllindexfootercenter"> <div class="xllindexfooterleft left" > <div class="xllindexfooterleftli"> <ul> <li><a href="/about.html">关于掌桥</a></li> <li><a href="/help/helpmap.html">资源导航</a></li> <li><a href="/help/helpguide.html">新手指南</a></li> <li><a href="/help/helpcenter.html">常见问题</a></li> <li><a href="/sitemap.html">网站地图</a></li> <li><a href="/help/helpcenter.html?type=9">版权声明</a></li> </ul> </div> <div class="xllindexfooterleft"> <p class="xllindexfooterlefteamil">客服邮箱：kefu@zhangqiaokeyan.com</p> <div class="xllindexfooterlefttcp"> <div class="xllindexfooterpoliceiimg"></div> <div class="xllindexfooterpoliceispan"> <span>京公网安备：11010802029741号 </span> <span>ICP备案号：<a href="https://beian.miit.gov.cn" rel="nofollow" target="_blank">京ICP备15016152号-6</a></span> <span>六维联合信息科技 (北京) 有限公司©版权所有</span> </div> </div> </div> </div> <div class="xllindexfooterright left"> <ul> <li> <p style="font-weight: bold;">客服微信</p> <div></div> </li> <li> <p style="font-weight: bold;">服务号</p> <div></div> </li> </ul> </div> </div> </div> <span id="0704025793861down" data-source="7," data-out-id="y5wyg/tepngAJzb5zapShRyr3L7C8btTPNc+oVaWKvNKoczaOiYesWmMHfIRQId4," data-f-source-id="7" data-title="Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ <i >9H9H ‐thioxanthenium hexafluorophosphates and 2,4‐dimethyl(diethyl)‐ <i >9H9H ‐thioxanthene‐9‐ones" data-price="20" data-site-name="" data-transnum="24" style="display:none;"></span> <input type="hidden" value="4" id="sourcetype"> <input type="hidden" value="35546" id="journalid"> <input type="hidden" value="https://cdn.zhangqiaokeyan.com" id="imgcdn"> <input type="hidden" value="1" id="isdeatail"> <input type="hidden" value="" id="syyn_indexed_database"> <input type="hidden" value="" id="servicetype"> <input type="hidden" id="pagename" value="Electrochemical reduction of 2,4‐dimethyl(diethyl)‐9‐oxo‐10‐(4‐heptoxyphenyl)‐ <i >9H9H ‐thioxanthenium hexafluorophosphates and 2,4‐dimethyl(diethyl)‐ <i >9H9H ‐thioxanthene‐9‐ones"/> <input type="hidden" value="thesis_get_original" id="pageIdentification"> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/jquery-1.12.4.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/lwlh_ajax.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/zq.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/common.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/jquery.cookie.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/top.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/tip.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/login.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/down.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/search.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/searchtype.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/user/regist.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/zxs_solor/detail.js?v=5.7.6"></script> <script type="text/javascript" src="https://www.zhangqiaokeyan.com/statistics/static/pagecollection.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/tj.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/pushbaidu.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/history.js"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/util/cookie.js?v=5.7.6"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/weipu/weipu.js?v=5.7.6"></script> </body> <script> $(function(){ var weiPuStatus = getCookie('WeiPuStatus'); if(weiPuStatus){ tipWeiPuStatus(weiPuStatus); delCookie('WeiPuStatus'); } getFacetKeywordVoInId(); var sourcetype = $("#sourcetype").val(); if(sourcetype ==1||sourcetype==4){ getJournal(); } }) </script> </html>