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Synthesis of Dihydrobenzoxazine‐Fused Spirooxazoline‐4‐ones via [3+2] Cycloaddition of Azaoxyallyl Cations with Vinyl Benzoxazinanones

机译:用乙烯基苯并嗪酮的亚沙氧基阳离子的亚沙氧基阳离子循环循环二氢苯并恶唑胺 - 熔融螺氧唑啉-4-孔的合成

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Abstract > An example of a [3+2] cycloaddition reaction between azaoxyallyl cations generated in?situ and a variety of vinyl benzoxazinanones has been developed. This reaction provides an attractive method for the synthesis of spirooxazoline‐4‐ones based on dihydrobenzoxazines, which were obtained in good yield (up to 98% yield) with high diastereoselectivity (up to 20?:?1). The synthesized spiro‐bis‐ N , O ‐heterocycles can be used as building blocks toward the synthesis of other useful compounds. </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> > 已经开发了在α原位和各种乙烯基苯并嗪酮的亚沙氧基阳离子之间的[3 + 2]环加入反应的实例。 该反应提供了合成基于二氢苯并嗪的螺氧唑啉-4-苯并异恶嗪的合成方法,其具有良好的产率(高达98%产率),具有高的非对映选择性(高达& 20?:1)。 合成的螺丝 - n </ i> 那 o </ i> - 呼吸依念可以用作合成其他有用的化合物的结构块。 </ 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11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"> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kim Eunjin&option=202" target="_blank" rel="nofollow">Kim Eunjin;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Mun Dasom&option=202" target="_blank" rel="nofollow">Mun Dasom;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kim Sung‐Gon&option=202" target="_blank" rel="nofollow">Kim Sung‐Gon;</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 ChemistryKyonggi University154-42 Gwanggyosan-ro Yeongtong-gu Suwon 16227 Republic of Korea;</p> <p>Department of ChemistryKyonggi University154-42 Gwanggyosan-ro Yeongtong-gu Suwon 16227 Republic of Korea;</p> <p>Department of ChemistryKyonggi University154-42 Gwanggyosan-ro Yeongtong-gu Suwon 16227 Republic of Korea;</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=spiro compounds&option=203" rel="nofollow">spiro compounds;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=dihydrobenzoxazines&option=203" rel="nofollow">dihydrobenzoxazines;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=tetrahydroisoquinolines&option=203" rel="nofollow">tetrahydroisoquinolines;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=cations&option=203" rel="nofollow">cations;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=benzoxazinanones&option=203" rel="nofollow">benzoxazinanones;</a> </p> <div class="translation"> 机译:螺铜化合物;二氢苯并嗪;四氢异喹啉;阳离子;苯并恶唑酮; 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href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=张翔&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,张翔</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=林紫云&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,林紫云</a> <span> <a href="/journal-cn-12157/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 结构化学 </a> </span> <span> . 2003</span><span>,第003期</span> </span> </div> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/academic-journal-cn_acta-chimica-sinica_thesis/0201272162522.html">4-(2'-羟基苯甲酰肼)苯亚甲基/亚乙基-5-甲基-2-苯基-2,4-二氢-吡唑啉酮-3超分子化合物的合成与晶体结构</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘浪&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 刘浪</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=吉亚丽&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,吉亚丽</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=贾殿赠&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,贾殿赠</a> <span> <a href="/journal-cn-53859/" target="_blank" rel="nofollow" class="tuijian_authcolor"> . 化学学报 </a> </span> <span> . 2003</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chinese-journal-synthetic-chemistry_thesis/0201234455650.html">3-N-(4-甲基苯基)氨基羰基-5-4-(4-甲酸基苯甲氧基)苯亚甲基-2,4-噻唑烷二酮的合成</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=郑礼康&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 郑礼康</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=金明&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,金明</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=张敬先&option=202" target="_blank" rel="nofollow" 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</span> <span> . 2018</span><span>,第006期</span> </span> </div> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/academic-journal-cn_chemical-journal-chinese-universities_thesis/0201231590720.html">3-甲基-1-苯基-4-{4-(5-甲基-2-(4-取代芳基)-噁唑-4-基甲氧基)-芳亚甲(苄)基}-2-吡唑啉-5-酮的设计、合成与降血糖活性</a> <b>[J]</b> <span> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=刘星&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor"> . 刘星</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=王亚楼&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,王亚楼</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=巫冠中&option=202" target="_blank" rel="nofollow" class="tuijian_auth tuijian_authcolor">,巫冠中</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> . 2007</span><span>,第004期</span> </span> </div> </li> <li> <div> <b>6. </b><a 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