...
首页> 外文期刊>Angewandte Chemie >Direct Arylation of α‐Amino C(sp3)‐H Bonds by Convergent Paired Electrolysis
【24h】

Direct Arylation of α‐Amino C(sp3)‐H Bonds by Convergent Paired Electrolysis

机译:通过收敛配对电解的α-氨基C(SP3)-H键的直接芳基化

获取原文
获取原文并翻译 | 示例
           

摘要

Abstract >A metal‐free convergent paired electrolysis strategy to synthesize benzylic amines through direct arylation of tertiary amines and benzonitrile derivatives at room temperature has been developed. This TEMPO‐mediated electrocatalytic reaction makes full use of both anodic oxidation and cathodic reduction without metals or stoichiometric oxidants, thus showing great potential and advantages for practical synthesis. This convergent paired electrolysis method provides a straightforward and powerful means to activate C?H bonds and realize cross‐coupling with cathodically generated species. </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”>抽象</ title> 已经开发了一种无金属收敛配对的电解策略,通过在室温下通过直接芳胺和苄腈衍生物的直接芳基合成苄基胺。 这种Tempo介导的电催化反应充分利用阳极氧化和阴极还原而没有金属或化学计量氧化剂,从而显示出实际合成的巨大潜力和优点。 该收敛配对的电解方法提供了一种直接和强大的方法,可激活C?H键并实现与阴极产生的物种的交叉耦合。</ p> </摘要> </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-19011/'>《Angewandte Chemie》</a> <b style="margin: 0 2px;">|</b><span>2019年第46期</span><b style="margin: 0 2px;">|</b><span>共5页</span> </div> </li> <li> <div class="author"> <span class="lefttit">作者</span> <p id="fAuthorthree" class="threelineshidden zhankaihshouqi"> </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"> </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/1188.html" title="应用化学">应用化学;</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=arylation&option=203" rel="nofollow">arylation;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=cross-coupling&option=203" rel="nofollow">cross-coupling;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=C?H activation&option=203" rel="nofollow">C?H activation;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=electrocatalysis&option=203" rel="nofollow">electrocatalysis;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=tertiary amines&option=203" rel="nofollow">tertiary amines;</a> </p> <div class="translation"> 机译:芳基化;交叉偶联;C?H激活;电殖分析;叔胺; </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/0704028165221.html">Direct Arylation of α‐Amino C(sp3)‐H Bonds by Convergent Paired Electrolysis</a> <b>[J]</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> <a href="/journal-foreign-19011/" target="_blank" rel="nofollow" class="tuijian_authcolor">Angewandte Chemie .</a> <span>2019</span><span>,第46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:通过收敛配对电解的α-氨基C(SP3)-H键的直接芳基化</span> </p> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-foreign_detail_thesis/0204120776452.html">Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lei Zhang&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Lei Zhang,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Xile Hu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Xile Hu </a> <a href="/journal-foreign-16127/" target="_blank" rel="nofollow" class="tuijian_authcolor">Chemical science .</a> <span>2020</span><span>,第39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:镍催化使收敛配对电解能够用于苄基C-H键的直接芳级</span> </p> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/0704022078652.html">Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C-H bonds</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Zhang Lei&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Zhang Lei,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Hu Xile&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Hu Xile </a> <a href="/journal-foreign-16125/" target="_blank" rel="nofollow" class="tuijian_authcolor">Chemical science .</a> <span>2020</span><span>,第39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:镍催化使收敛配对电解能够用于苄基C-H键的直接芳级</span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-conference-foreign_meeting-252588_thesis/0705010227028.html">Direct C-H Bond Arylation of Arenes with Aryltin Reagents Catalyzed by Palladium Complexes</a> <b>[C]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Hiroshi Kawai&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Hiroshi Kawai,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Yasuhiro Kobayashi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Yasuhiro Kobayashi,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Shuichi Oi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Shuichi Oi </a> <a href="/conference-foreign-252588/" target="_blank" rel="nofollow" class="tuijian_authcolor">Symposium on Organometallic Chemistry .</a> <span>2007</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:用钯配合物催化的芳in试剂直接C-H键芳苯化</span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-degree-foreign_mphd_thesis/02061452762.html">Palladium-mediated carbon-carbon bond formation: Methodology and mechanism. Part I: Palladium-catalyzed alpha-arylation of aryl nitromethanes, phosphonoacetates, and phosphine oxides. Part II: Mechanistic study of the palladium-mediated chemoselective activation of C(sp3)-H bonds.</a> <b>[D] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=VanGelder, Kelsey Faith.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">VanGelder, Kelsey Faith. </a> <span>2016</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:钯介导的碳-碳键形成:方法和机理。第一部分:芳族硝基甲烷,膦酰基乙酸酯和氧化膦的钯催化α-芳基化反应。第二部分:钯介导的C(sp3)-H键的化学选择性激活的机理研究。</span> </p> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-journal-foreign-pmc_detail_thesis/040006635897.html">Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lei Zhang&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Lei Zhang,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Xile Hu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Xile Hu </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:镍催化使收敛配对电解能够用于苄基C-H键的直接芳级</span> </p> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/open-access_resources_thesis/01000125827664.html">Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lei Zhang&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Lei Zhang,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Xile Hu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Xile Hu </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:镍催化使收敛配对电解能够用于苄基C-H键的直接芳级</span> </p> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/academic-journal-cn_applied-chemical-industry_thesis/0201248422071.html">Pd(OAc)2/CuI共催化杂环C—H键与芳基溴的直接芳基化反应研究</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=颜雪明&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 颜雪明</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=肖新荣&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,肖新荣</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=谭倪&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,谭倪</a> <span> <a href="/journal-cn-9217/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 应用化工 </a> </span> <span> . 2012</span><span>,第008期</span> </span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-dezhou-university_thesis/0201235454313.html">芳环C-H键直接芳基化反应研究进展</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=华晓莹&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 华晓莹</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=辛炳炜&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,辛炳炜</a> <span> <a href="/journal-cn-3933/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 德州学院学报 </a> </span> <span> . 2010</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-yunnan-normal-university-natural-sciences-edition_thesis/0201248113150.html">铜催化芳杂环C-H键区域选择性芳基化的研究进展</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=黄国利&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 黄国利</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘波&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,刘波</a> <span> <a href="/journal-cn-4525/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 云南师范大学学报(自然科学版) </a> </span> <span> . 2014</span><span>,第001期</span> </span> </div> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-applied-chemistry_thesis/0201272091565.html">pd(Ⅱ)催化的芳基次膦酸衍生物C—H键活化芳基化反应及衍生化反应</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=关静&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 关静</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=吴国杰&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,吴国杰</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=韩福社&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,韩福社</a> <span> <a href="/journal-cn-54377/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 应用化学 </a> </span> <span> . 2014</span><span>,第011期</span> </span> </div> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chemical-journal-chinese-universities_thesis/0201231588878.html">二茂铁亚胺环钯化合物催化的带有导向基团的sp2C-H键底物的邻位芳基化</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李亚楠&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 李亚楠</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=杨帆&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,杨帆</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=吴养洁&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,吴养洁</a> <span> <a href="/journal-cn-10958/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 高等学校化学学报 </a> </span> <span> . 2008</span><span>,第012期</span> </span> </div> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-conference-cn_meeting-43259_thesis/020222758080.html">O-苄基羟胺与丙酸乙酯经缩合、Pd催化C(sp2)-H键芳基化和苄基C-O键溶剂解反应序列合成2-芳基苄基乙酸酯</a> <b>[C]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Ling-Yan Shao&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . Ling-Yan Shao</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=邵玲艳&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,邵玲艳</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Li-Hao Xing&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,Li-Hao Xing</a> <span> <a href="/conference-cn-43259/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 中国药学会制药工程专业委员会2017年学术年会暨药包材与药品关联审评审批研讨会 </a> <span> <span> . 2017</span> </span> </div> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/academic-degree-domestic_mphd_thesis/020316057779.html">天然氨基酸导向的多肽C(sp3)‒H键芳基化反应研究</a> <b>[A] </b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=丁星星&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 丁星星</a> <span> . 2020</span> </span> </div> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/06120113499694.html">一种C(sp3)-C(sp2)键的构建方法与β-芳基氨基酸的制备方法</a> <b>[P]</b> . <span> 中国专利: CN113527121A </span> <span> . 2021-10-22</span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/061204540315.html">一种钯催化羧酸导向的γ-C(sp<Sup>3</Sup>)-H键芳基化合成大位阻氨基酸或多肽的方法</a> <b>[P]</b> . <span> 中国专利: CN110776455B </span> <span> . 2021.07.20</span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130401775697.html">Directed Beta-C(sp3)–H Iodination and Arylation of Ketones</a> <b>[P]</b> . <span> 外国专利: <!-- 美国专利: --> US2020255363A1 </span> <span> . 2020-08-13</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:定向β-C(sp3)–H碘化和酮的芳构化 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130403585641.html">DIRECTED B-C(SP3)-H IODINATION AND ARYLATION OF KETONES</a> <b>[P]</b> . <span> 外国专利: <!-- 世界知识产权组织专利: --> WO2019036349A1 </span> <span> . 2019-02-21</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:酮的B-C(SP3)-H定向和芳构化 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130403585640.html">DIRECTED B-C(SP3)-H IODINATION AND ARYLATION OF KETONES</a> <b>[P]</b> . <span> 外国专利: <!-- 世界知识产权组织专利: --> WO2019036349A8 </span> <span> . 2019-05-09</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:酮的B-C(SP3)-H定向和芳构化 </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('0704028165221','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="关闭" 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)" title="意见反馈">意见反馈</a> </li> <li class="top"> <a href="javascript:scrollTo(0,0);" title="回到顶部">回到顶部</a> </li> <li class="shouye"> <a href="/" title="首页">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" title="关于掌桥">关于掌桥</a></li> <li><a href="/help/helpmap.html" title="资源导航">资源导航</a></li> <li><a href="/help/helpguide.html" title="新手指南">新手指南</a></li> <li><a href="/help/helpcenter.html" title="常见问题">常见问题</a></li> <li><a href="/sitemap.html" title="网站地图">网站地图</a></li> <li><a href="/help/helpcenter.html?type=9" title="版权声明">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" title="ICP备案号">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="0704028165221down" data-source="7," data-out-id="P9baPokr2l2liLAdifQCdhLS3/545hOYUHNo2Utyn9ekkvg+IjAO9qOt9pQbY15y," data-f-source-id="7" data-title="Direct Arylation of α‐Amino C(sp3)‐H Bonds by Convergent Paired Electrolysis" data-price="20" data-site-name="" data-transnum="24" style="display:none;"></span> <input type="hidden" value="4" id="sourcetype"> <input type="hidden" value="19011" id="journalid"> <input type="hidden" value="1" id="inyn_provide_service_level"> <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="Direct Arylation of α‐Amino C(sp3)‐H Bonds by Convergent Paired Electrolysis"/> <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=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/common.js?v=5.7.8"></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=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/tip.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/login.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/down.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/search.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/newmail.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/searchtype.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/user/regist.js?v=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/zxs_solor/detail.js?v=5.7.8"></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/common/sse.js?v=5.7.8"></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=5.7.8"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/weipu/weipu.js?v=5.7.8"></script> </body> <script> $(function(){ var weiPuStatus = getCookie('WeiPuStatus'); if(weiPuStatus){ tipWeiPuStatus(weiPuStatus); delCookie('WeiPuStatus'); } getFacetKeywordVoInId(); var sourcetype = $("#sourcetype").val(); var inyn_provide_service_level = $("#inyn_provide_service_level").val(); if((sourcetype ==1||sourcetype==4)&&inyn_provide_service_level!=4){ getJournal(); } }) </script> </html>