• 主题
高级搜索  >
历史搜索 清空历史
首页> 外文期刊>Asian Journal of Organic Chemistry >Metal‐Free Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐Ones via Cascade Oxidative Decarbonylative Radical Alkylation/Cyclization of Cinnamamides with Aliphatic Aldehydes
【24h】

Metal‐Free Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐Ones via Cascade Oxidative Decarbonylative Radical Alkylation/Cyclization of Cinnamamides with Aliphatic Aldehydes

机译：通过级联氧化脱羰基烷基化自由基烷基化/环化与脂族醛的无金属合成3,4-二氢喹啉-2（1H） - 环化

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 > A practical and efficient method for synthesis of alkyl‐substituted 3,4‐dihydroquinolin‐2(1 H )‐ones via cascade oxidative decarbonylative radical alkylation/cyclization of cinnamamides with aliphatic aldehydes under metal‐free conditions was developed. The reaction offers a complementary approach of regioselective intramolecular 6‐ endo ‐ trig cyclization of cinnamamides with various primary, secondary and tertiary alkyl radicals generated from aliphatic aldehydes. </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> > 合成烷基取代的3,4-二氢喹啉-2（1的实用有效的方法（1 h </ i> （通过Cascade氧化脱羰基烷基化烷基化/环化的肉桂酰胺与无金属条件下的脂族醛烷基化烷基化/环化。 反应提供了分子分子内的互补方法6- endo </ i> - trig </ i> 用脂族醛产生的各种初级，次级和叔烷基的肉桂酰胺环化。 </ 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-19765/'>《Asian Journal of Organic Chemistry》</a> <b style="margin: 0 2px;">|</b><span>2019年第10期</span><b style="margin: 0 2px;">|</b><span>共4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=Xu Xuemei&option=202" target="_blank" rel="nofollow">Xu Xuemei;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Luo Zaigang&option=202" target="_blank" rel="nofollow">Luo Zaigang;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Liu Chen‐Fu&option=202" target="_blank" rel="nofollow">Liu Chen‐Fu;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Wang Xiuxiu&option=202" target="_blank" rel="nofollow">Wang Xiuxiu;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Deng Liangdan&option=202" target="_blank" rel="nofollow">Deng Liangdan;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Gao Jie&option=202" target="_blank" rel="nofollow">Gao Jie;</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>College of Chemical EngineeringAnHui University of Science and TechnologyHuainan 232001 China;</p> <p>College of Chemical EngineeringAnHui University of Science and TechnologyHuainan 232001 China;</p> <p>School of Pharmaceutical ScienceGannan Medical UniversityGanzhou 341000 China;</p> <p>College of Chemical EngineeringAnHui University of Science and TechnologyHuainan 232001 China;</p> <p>College of Chemical EngineeringAnHui University of Science and TechnologyHuainan 232001 China;</p> <p>College of Chemical EngineeringAnHui University of Science and TechnologyHuainan 232001 China;</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/1184.html" title="有机化学">有机化学;</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=radical cyclization&option=203" rel="nofollow">radical cyclization;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=3&option=203" rel="nofollow">3;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=4-dihydroquinolin-2(1H)-one&option=203" rel="nofollow">4-dihydroquinolin-2(1H)-one;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=oxidative decarbonylation&option=203" rel="nofollow">oxidative decarbonylation;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=aliphatic aldehyde&option=203" rel="nofollow">aliphatic aldehyde;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=cinnamamide&option=203" rel="nofollow">cinnamamide;</a> </p> <div class="translation"> 机译：自由基环化;3;4-二氢喹啉-2（1H） - 氧化脱羰;脂族醛;肉桂酰胺; </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/0704022773505.html">Metal‐Free Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐Ones via Cascade Oxidative Decarbonylative Radical Alkylation/Cyclization of Cinnamamides with Aliphatic Aldehydes</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Xu Xuemei&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Xu Xuemei,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Luo Zaigang&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Luo Zaigang,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Liu Chen‐Fu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Liu Chen‐Fu,</a> <a href="/journal-foreign-19765/" target="_blank" rel="nofollow" class="tuijian_authcolor">Asian Journal of Organic Chemistry .</a> <span>2019</span><span>,第10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：通过级联氧化脱羰基烷基化自由基烷基化/环化与脂族醛的无金属合成3,4-二氢喹啉-2（1H） - 环化</span> </p> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/070403151250.html">Metal-Free Oxidative Decarbonylative Coupling of Aliphatic Aldehydes with Azaarenes: Successful Minisci-Type Alkylation of Various Heterocycles</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Tang Ren-Jin&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Tang Ren-Jin,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kang Lei&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Kang Lei,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Yang Luo&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Yang Luo </a> <a href="/journal-foreign-19407/" target="_blank" rel="nofollow" class="tuijian_authcolor">Advanced synthesis & catalysis .</a> <span>2015</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：脂肪族醛与氮杂芳烃的无金属氧化脱羰基偶联：各种杂环的成功Minisci型烷基化</span> </p> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-foreign_organic-and-biomolecular-chemistry_thesis/0204111642779.html">Metal-free oxidative decarbonylative alkylation of chromones using aliphatic aldehydes</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Rongzhen Chen&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Rongzhen Chen,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Jin-Tao Yu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Jin-Tao Yu,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Jiang Cheng&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Jiang Cheng </a> <a href="/journal-foreign-696/" target="_blank" rel="nofollow" class="tuijian_authcolor">Organic & biomolecular chemistry .</a> <span>2018</span><span>,第19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：使用脂肪族醛的色酮的无金属氧化脱羰基烷基化</span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-conference-foreign_meeting-264997_thesis/0705014518995.html">Selective Synthesis of α-Chloroepoxides by Electro-reductive Cross-Coupling of Methyl Trichloro-acetate with Aliphatic Aldehydes Using Reactive Metal Anode</a> <b>[C]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Ikuzo Nishiguchi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Ikuzo Nishiguchi,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Satoshi Goda&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Satoshi Goda,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Takeshi Kikkawa&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Takeshi Kikkawa </a> <a href="/conference-foreign-264997/" target="_blank" rel="nofollow" class="tuijian_authcolor">The Meeting of the Electrochemical Society .</a> <span>2001</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：用反应金属阳极用脂族醛的电解交叉偶联选择性合成α-氯环氧化物</span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-degree-foreign_mphd_thesis/02061434169.html">I. Chemoselective catalytic hydrogenation of alpha, beta-unsaturated aldehydes and ketones using soluble copper(I) hydrides II. Free radical alkylation of titanium(III) allyl and propargyl complexes.</a> <b>[D] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Chen, Jianxian.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Chen, Jianxian. </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：I.使用可溶的氢化铜（I）对α，β-不饱和醛和酮进行化学选择性催化氢化。钛（III）烯丙基和炔丙基复合物的自由基烷基化。</span> </p> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-journal-foreign-pmc_detail_thesis/040005469022.html">A new cascade halosulfonylation of 17-enynes toward 34-dihydroquinolin-2(1H)-ones via sulfonyl radical-triggered addition/6-exo-dig cyclization</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Yi-Long Zhu&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Yi-Long Zhu,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Bo Jiang&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Bo Jiang,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Wen-Juan Hao&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Wen-Juan Hao,</a> <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：通过磺酰基基团触发的加成/ 6-外切-dig环化反应将17-烯炔向34-二氢喹啉-2（1H）-的新级联磺酰化</span> </p> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/open-access_resources_thesis/01000127787754.html">Metal-Free Cascade Oxidative Decarbonylative Alkylation/Arylation of Alkynoates with Alphatic Aldehydes</a> <b>[O] </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>-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：无金属级联氧化脱氧羰基化烷基化/炔烃芳酸盐与年性醛酸盐</span> </p> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-applied-chemistry_thesis/0201272092454.html">可见光诱导烯烃环化合成二氟烷基化异喹啉二酮</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李捷&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 李捷</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘益林&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,刘益林</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=邓佑林&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,邓佑林</a> <span> <a href="/journal-cn-54377/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 应用化学 </a> </span> <span> . 2016</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-applied-chemistry_thesis/0201272092457.html">可见光诱导烯烃串联加成环化合成多氟烷基化异喹啉二酮</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=邓佑林&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 邓佑林</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=唐石&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,唐石</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=张倩&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,张倩</a> <span> <a href="/journal-cn-54377/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 应用化学 </a> </span> <span> . 2016</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-cn_detail_thesis/0201297727165.html">基于N-肉桂基磺酰胺的环化硫氰化合成3,4-二取代的1,2,3,4-四氢喹啉硫氰酸酯</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=陈甫雪&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 陈甫雪</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=袁乐霞&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,袁乐霞</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=邱佳申&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,邱佳申</a> <span> <a href="/journal-cn-56810/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 北京理工大学学报 </a> </span> <span> . 2021</span><span>,第5期</span> </span> </div> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-zhejiang-normal-university-natural-sciences_thesis/0201270211325.html">麦克尔/环化串联反应高效合成多官能团的3,4-二氢-2H-硫吡喃2,3-b喹啉</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=高志坚&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 高志坚</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=王梦雪&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,王梦雪</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=王经&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,王经</a> <span> <a href="/journal-cn-4541/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 浙江师范大学学报（自然科学版） </a> </span> <span> . 2019</span><span>,第003期</span> </span> </div> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-synthetic-chemistry_thesis/0201234504779.html">新的苯并二氮(艹卓)类三环化合物：1H,10H-4,9-二氢-环戊并1,2-b1,5苯并二氮(艹卓)-10-酮及其3-甲基衍生物的合成</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=杨彬&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 杨彬</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=恽榴红&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,恽榴红</a> <span> <a href="/journal-cn-11569/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 合成化学 </a> </span> <span> . 1996</span><span>,第002期</span> </span> </div> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-conference-cn_meeting-58797_thesis/020222551968.html">6-2-(4-苯甲基哌嗪基)乙酰氨基-3,4-二氢-2(1H)-喹啉桐衍生物的合成及正性肌力活性研究</a> <b>[C]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=朴虎日&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 朴虎日</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=全哲山&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,全哲山</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=赵立明&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,赵立明</a> <span> <a href="/conference-cn-58797/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 2001中国药学会学术年会 </a> <span> <span> . 2001</span> </span> </div> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/academic-degree-domestic_mphd_thesis/020315559284.html">电化学氧化的吲哚对映选择性烷基化及肟自由基参与的分子内串联环化反应研究</a> <b>[A] </b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=路佛云&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 路佛云</a> <span> . 2020</span> </span> </div> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/061204200481.html">利用双氧化脱氢环化反应合成3,4-二氢喹啉-3酮类化合物的方法</a> <b>[P]</b> . <span> 中国专利： CN109293568B </span> <span> . 2021.01.12</span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/06120100123917.html">利用双氧化脱氢环化反应合成3,4-二氢喹啉-3酮类化合物的方法</a> <b>[P]</b> . <span> 中国专利： CN109293568A </span> <span> . 2019-02-01</span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130423017742.html">Method for the use of <Sup>11 </Sup>C carbon monoxide in labeling synthesis of <Sup>11</Sup>C-labelled amides using metal amides and photo-induced free radical carbonylation</a> <b>[P]</b> . <span> 外国专利： <!-- 美国专利： --> US8129528B2 </span> <span> . 2012-03-06</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：[<Sup> 11 </ Sup> C]一氧化碳在金属酰胺标记和光诱导自由基羰基化标记<Sup> 11 </ Sup> C标记酰胺中的应用 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130428157074.html">METHOD FOR THE USE OF 11C CARBON MONOXIDE IN LABELING SYNTHESIS OF 11C-LABELLED AMIDES USING METAL AMIDES AND PHOT-INDUCED FREE RADICAL CARBONYLATION</a> <b>[P]</b> . <span> 外国专利： <!-- 美国专利： --> US2009297445A1 </span> <span> . 2009-12-03</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：[11C]一氧化碳在金属酰胺标记和光诱导的自由基羰基化合成11C标记的酰胺中的使用方法 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130430547526.html">Method for the use of <Sup>11</Sup>C carbon monoxide in labeling synthesis of <Sup>11</Sup>C-labelled amides using metal amides and photo-induced free radical carbonylation</a> <b>[P]</b> . <span> 外国专利： <!-- 美国专利： --> US7553942B2 </span> <span> . 2009-06-30</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：[<Sup> 11 </ Sup> C]一氧化碳在金属酰胺标记和光诱导自由基羰基化标记<Sup> 11 </ Sup> C标记的酰胺中的应用 </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('0704022773505','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="0704022773505down" data-source="7," data-out-id="+U7M5R7pIKW+5hkylIyiZtZFxHNKDggyZtgsnOM3OcfbQ1t3b0JLO/Rn8UbxPOC4," data-f-source-id="7" data-title="Metal‐Free Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐Ones via Cascade Oxidative Decarbonylative Radical Alkylation/Cyclization of Cinnamamides with Aliphatic Aldehydes" data-price="20" data-site-name="" data-transnum="24" style="display:none;"></span> <input type="hidden" value="4" id="sourcetype"> <input type="hidden" value="19765" 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="Metal‐Free Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐Ones via Cascade Oxidative Decarbonylative Radical Alkylation/Cyclization of Cinnamamides with Aliphatic Aldehydes"/> <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=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/common.js?v=5.7.7"></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=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/tip.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/login.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/down.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/common/search.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/searchtype.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/user/regist.js?v=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/zxs_solor/detail.js?v=5.7.7"></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=5.7.7"></script> <script type="text/javascript" src="https://cdn.zhangqiaokeyan.com/js/weipu/weipu.js?v=5.7.7"></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>