首页> 外文期刊>Chemical record >Microwave Flow Chemistry as a Methodology in Organic Syntheses, Enzymatic Reactions, and Nanoparticle Syntheses

【24h】

Microwave Flow Chemistry as a Methodology in Organic Syntheses, Enzymatic Reactions, and Nanoparticle Syntheses

机译：微波流动化学作为有机合成，酶反应和纳米颗粒合成的方法

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Abstract >Several studies have used microwaves as a heat source for carrying out various types of reactions employing circulation reaction vessels. The microwave flow chemical synthesis methodology is most appropriate in the use of microwaves in chemical syntheses. It can attenuate the problem of microwave heating (non‐uniform heating and penetration depth) and maximize the benefits (rapid heating and first temperature adjustments). In this brief review, we examine and explain some of the relevant features of microwave heating with applicative examples of the usage of microwave flow chemistry equipment in carrying out organic syntheses, enzymatic reactions, and (not least) nanoparticle syntheses. </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> >几项研究用微波炉作为热源，用于进行采用循环反应的各种类型的反应船只。微波流量化学合成方法最适合在化学合成中使用微波。它可以衰减微波加热（不均匀加热和穿透深度）的问题，并最大限度地提高益处（快速加热和第一温度调节）。在这篇简短的综述中，我们检查并解释了微波加热的一些相关特征，其使用微波流化化学设备在进行有机合成，酶促反应和（尤其是纳米颗粒合成中的微波流化学设备的应用示例。</ 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-16132/'>《Chemical record》</a> <b style="margin: 0 2px;">|</b><span>2019年第1期</span><b style="margin: 0 2px;">|</b><span>共22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=Horikoshi Satoshi&option=202" target="_blank" rel="nofollow">Horikoshi Satoshi;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Serpone Nick&option=202" target="_blank" rel="nofollow">Serpone Nick;</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>Department of Materials and Life Sciences Faculty of Science and TechnologySophia University7-1 Kioicho Chiyodaku Tokyo 102-8554 Japan;</p> <p>PhotoGreen Laboratory Dipartimento di ChimicaUniversita di PaviaVia Taramelli 12 Pavia 27100 Italy;</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/159.html" title="化学">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=Microwave heating&option=203" rel="nofollow">Microwave heating;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Microwave organic flow synthesis&option=203" rel="nofollow">Microwave organic flow synthesis;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Microwave-assisted catalyzed flow reactions&option=203" rel="nofollow">Microwave-assisted catalyzed flow reactions;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Microwave flow synthesis of biomaterials&option=203" rel="nofollow">Microwave flow synthesis of biomaterials;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Microwave flow synthesis of nanoparticles&option=203" rel="nofollow">Microwave flow synthesis of nanoparticles;</a> </p> <div class="translation"> 机译：微波加热;微波有机流量合成;微波辅助催化流动反应;微波流量合成生物材料;微波流量合成纳米粒子; </div> </li> <li> <span class="lefttit">入库时间</span> <span>2022-08-19 23:33:24</span> </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/0704022080032.html">Microwave Flow Chemistry as a Methodology in Organic Syntheses, Enzymatic Reactions, and Nanoparticle Syntheses</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Horikoshi Satoshi&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Horikoshi Satoshi,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Serpone Nick&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Serpone Nick </a> <a href="/journal-foreign-16132/" target="_blank" rel="nofollow" class="tuijian_authcolor">Chemical record .</a> <span>2019</span><span>,第1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：微波流动化学作为有机合成，酶反应和纳米颗粒合成的方法</span> </p> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/0704016430126.html">Development of novel asymmetric reactions oriented to next-generation enzymatic organic syntheses</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Akai S&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Akai S </a> <a href="/journal-foreign-36982/" target="_blank" rel="nofollow" class="tuijian_authcolor">藥學雜誌 .</a> <span>2003</span><span>,第11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：面向下一代酶促有机合成的新型不对称反应的开发</span> </p> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/0704026518807.html">Development of novel asymmetric reactions oriented to next-generation enzymatic organic syntheses</a> <b>[J]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Akai S&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Akai S </a> <a href="/journal-foreign-36982/" target="_blank" rel="nofollow" class="tuijian_authcolor">藥學雜誌 .</a> <span>2003</span><span>,第11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：发展到下一代酶有机合成的新型不对称反应</span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-conference-foreign_meeting-213685_thesis/020514773367.html">Organic Syntheses in Unconventional Reaction Media</a> <b>[C]</b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Francesco Fringuelli&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Francesco Fringuelli,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Oriana Piermatti&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Oriana Piermatti,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Ferdinando Pizzo&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Ferdinando Pizzo </a> <a href="/conference-foreign-213685/" target="_blank" rel="nofollow" class="tuijian_authcolor">Edition of the A. Corbella" summer school on organic synthesis" .</a> <span>1998</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：非常规反应介质中的有机合成</span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-degree-foreign_mphd_thesis/02061641721.html">Syntheses and functionalizations of magnetic iron oxide nanoparticles for applications in organic chemistry</a> <b>[D] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Li, Guifeng&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Li, Guifeng </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：磁性氧化铁纳米粒子的合成和功能化，用于有机化学</span> </p> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-journal-foreign-pmc_detail_thesis/040006054675.html">The Application of Vinylogous Iminium Salt Derivatives and Microwave Accelerated Vilsmeier-Haack Reactions to Efficient Relay Syntheses of the Polycitone and Storniamide Natural Products</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=John T. Gupton&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">John T. Gupton,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Edith J. Banner&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Edith J. Banner,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Melissa D. Sartin&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Melissa D. Sartin,</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：含乙烯基亚胺盐衍生物和微波加速的Vilsmeier-Haack反应在聚citone和Storniamide天然产物高效中继合成中的应用</span> </p> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/open-access_resources_thesis/01000127945308.html">Syntheses and Reactions in Organic Chemistry (Parham, William E.)</a> <b>[O] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Joesph V. Paukstelis&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Joesph V. Paukstelis </a> <span>1971</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：有机化学中的合成和反应（帕拉姆，威廉E.）</span> </p> </li> <li> <div> <b>8. </b><a class="enjiyixqcontent" href="/ntis-science-report_ad_thesis/020711400202.html">Syntheses of (Difluoroamino)Difluoroacetonitrile, Syn-Fluoro(Fluoroimino)Acetonitrile, and Syn-3,3,3-Trifluoro-2-(Fluoroimino)Propanenitrile and Their Reactions with Chlorine Fluoride. Syntheses of New Perfluorinated Diazines</a> <b>[R] </b> . <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Marsden, H. M.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Marsden, H. M.,</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Shreeve, J. M.&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">Shreeve, J. M. </a> <span>1987</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：合成（二氟氨基）二氟乙腈，syn-Fluoro（氟代亚氨基）乙腈和syn-3,3,3-三氟-2-（氟代亚氨基）丙腈及其与氯氟化物的反应。新型全氟化二嗪的合成</span> </p> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-organic-chemistry_thesis/0201293626557.html">中译本《不对称有机催化》、《合成中的副反应》、《当代有机氟化学》和《当代有机合成方法》出版发行</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> <span> <a href="/journal-cn-15847/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 有机化学 </a> </span> <span> . 2006</span><span>,第5期</span> </span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-east-china-university-science-technology-natural-edition_thesis/0201262632341.html">化学气相冷凝合成纳米颗粒反应器研究：Ⅰ.流体流动过 …</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=孙志刚&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 孙志刚</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=朱以华&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,朱以华</a> <span> <a href="/journal-cn-50120/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 华东理工大学学报：自然科学版 </a> </span> <span> . 1998</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-cn_journal-east-china-university-science-technology-social-edition_thesis/0201283282820.html">化学气相冷凝合成纳米颗粒反应器研究 I.流体流动过程模拟</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=孙志刚&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 孙志刚</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=朱以华&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,朱以华</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李春忠&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,李春忠</a> <span> <a href="/journal-cn-1368/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 华东理工大学学报：社会科学版 </a> </span> <span> . 1998</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/academic-journal-cn_microwave-chemistry_thesis/0201272674982.html">微波催化有机合成化学反应</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘明1&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 刘明1</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=胡文祥2&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,胡文祥2</a> <span> <a href="/journal-cn-38945/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 微波化学 </a> </span> <span> . 2018</span><span>,第003期</span> </span> </div> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-journal-cn_technology-development-chemical-industry_thesis/0201233247523.html">微波促进有机反应原理及微波有机合成仪</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李永红&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 李永红</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=李跃明&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,李跃明</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=沈玲&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,沈玲</a> <span> <a href="/journal-cn-11275/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 化工技术与开发 </a> </span> <span> . 2006</span><span>,第003期</span> </span> </div> </li> <li> <div> <b>6. </b><a class="enjiyixqcontent" href="/academic-conference-cn_meeting-28843_thesis/020222082965.html">S-烯丙醇酮合成研究——有机相中酶催化不对称合成反应的应用</a> <b>[C]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=陈慧新&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 陈慧新</a> <span> <a href="/conference-cn-28843/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 中国拟除虫菊酯发展三十年学术研讨会 </a> <span> <span> . 2003</span> </span> </div> </li> <li> <div> <b>7. </b><a class="enjiyixqcontent" href="/academic-degree-domestic_mphd_thesis/020314953815.html">二碘化钐、金属镱促进的有机化学反应在有机合成中的应用及5-溴苯酞的合成研究</a> <b>[A] </b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=高宁&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 高宁</a> <span> . 2002</span> </span> </div> </li> </ul> <ul style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/061204326617.html">一种基于流动化学酶促胺解反应在线合成苯乙醇类β-氨基醇衍生物的方法</a> <b>[P]</b> . <span> 中国专利： CN109706194B </span> <span> . 2021.04.06</span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/06120100567316.html">一种基于流动化学酶促胺解反应在线合成苯乙醇类β-氨基醇衍生物的方法</a> <b>[P]</b> . <span> 中国专利： CN109706194A </span> <span> . 2019-05-03</span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130437780743.html">Polyethylene glycol-based macromonomers, chemically inert polymers prepared from such macromonomers and use of these polymers in organic syntheses and enzymatic reactions</a> <b>[P]</b> . <span> 外国专利：  CZ296517B6 </span> <span> . 2006-04-12</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：聚乙二醇基大分子单体，由此类大分子单体制备的化学惰性聚合物，以及这些聚合物在有机合成和酶促反应中的用途 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130449088039.html">Macromonomers based on polyethylene glycols, chemically inert polymers prepared from these macromonomers and use of these polymers for organic syntheses and enzymatic reactions</a> <b>[P]</b> . <span> 外国专利：  CZ20011037A3 </span> <span> . 2001-08-15</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：基于聚乙二醇的大分子单体，由这些大分子单体制备的化学惰性聚合物，以及这些聚合物在有机合成和酶促反应中的用途 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130433971390.html">New optically active organo phosphorus compound useful to prepare phosphine-metal catalysts useful to carry out asymmetrical syntheses in organic chemistry</a> <b>[P]</b> . <span> 外国专利：  FR2887253A1 </span> <span> . 2006-12-22</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：用于制备膦金属催化剂的新型旋光有机磷化合物，可用于在有机化学中进行不对称合成 </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('0704022080032','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">  </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="0704022080032down" data-source="7," data-out-id="e1Hk9poIlUmsUdZS5jBfpcDiZnELJzYwA9pn306OFrtQg16MOLtR0VL2bYztzo0v," data-f-source-id="7" data-title="Microwave Flow Chemistry as a Methodology in Organic Syntheses, Enzymatic Reactions, and Nanoparticle Syntheses" data-price="20" data-site-name="" data-transnum="24" style="display:none;"></span> <input type="hidden" value="4" id="sourcetype"> <input type="hidden" value="16132" 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="Microwave Flow Chemistry as a Methodology in Organic Syntheses, Enzymatic Reactions, and Nanoparticle Syntheses"/> <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>