Abstract Several classes of arylphosphorus acid amides have been tested in reactions with alkali metal solutions in liquid ammonia. The outcome"/>

The Reactivity of Arylphosphorus Acid Amides Under Birch Reduction Conditions

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY(2013)

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Abstract Several classes of arylphosphorus acid amides have been tested in reactions with alkali metal solutions in liquid ammonia. The outcomes of such reactions depend on the structures of the starting materials. Generally, two processes - Birch reduction or cleavage of the P-aryl bond - can be operative. Diarylphosphinic amides tend to undergo double Birch reduction to afford bis(cyclohexadienyl)phosphinic amides.</div><span class="a-aminer-core-pub-c-paper-abstract-morebtn"><span>更多</span></span></div></div><div class="a-aminer-core-pub-c-paper-abstract-tranText">查看译文</div></div></div></div></span></div></div><div class="a-aminer-core-pub-index-titleBox"><div class="a-aminer-core-pub-index-keyTitle">关键词</div><div class="a-aminer-core-pub-index-titleKeys"><span>Synthetic methods<!-- -->,</span><span>Organophosphorus chemistry<!-- -->,</span><span>Phosphorus<!-- -->,</span><span>Reduction</span></div></div></div><div class="background" style="margin-top:16px;margin-bottom:16px" id="summary"><div class="mainTitle"><span>AI 理解论文</span></div><div><div class="stitle" style="margin-top:16px;margin-bottom:16px"><span>溯源树</span></div><div class="a-aminer-core-pub-index-renderTree"><div class="a-aminer-core-pub-index-example"><div class="a-aminer-core-pub-index-topExampleText"><span>样例</span></div><img src="https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg" alt=""/></div><div class="a-aminer-core-pub-index-layer"></div><div class="a-aminer-core-pub-index-pdfLoad"><div class="a-aminer-core-pub-index-pdfLoad_text"><span style="margin-right:24px"><svg class="icon" aria-hidden="true"><use xlink:href="#icon-suyuansu"></use></svg></span><span>生成溯源树,研究论文发展脉络</span></div></div></div></div></div></section><div><div class=""><section class="a-aminer-core-pub-index-rightBar"><div class="a-aminer-core-pub-index-commented "><div class="a-aminer-core-pub-index-bg"></div><div class="a-aminer-core-pub-index-title">Chat Paper</div><div class="a-core-home2-c-card-person-bottom-card-new-summary-index-summaryBox a-core-home2-c-card-person-bottom-card-new-summary-index-pubBox"><div class="a-core-home2-c-card-person-bottom-card-new-summary-index-loadingBox"><span class="a-core-home2-c-card-person-bottom-card-new-summary-index-loadingText">正在生成论文摘要</span><div class="ant-spin ant-spin-spinning"><i aria-label="icon: loading" style="font-size:24px" class="anticon anticon-loading ant-spin-dot"><svg viewBox="0 0 1024 1024" focusable="false" class="anticon-spin" data-icon="loading" width="1em" height="1em" fill="currentColor" aria-hidden="true"><path d="M988 548c-19.9 0-36-16.1-36-36 0-59.4-11.6-117-34.6-171.3a440.45 440.45 0 0 0-94.3-139.9 437.71 437.71 0 0 0-139.9-94.3C629 83.6 571.4 72 512 72c-19.9 0-36-16.1-36-36s16.1-36 36-36c69.1 0 136.2 13.5 199.3 40.3C772.3 66 827 103 874 150c47 47 83.9 101.8 109.7 162.7 26.7 63.1 40.2 130.2 40.2 199.3.1 19.9-16 36-35.9 36z"></path></svg></i></div></div></div></div></section></div></div></article></main></main></section></div> <script> window.g_useSSR = true; window.g_initialProps = {"global":{"collapsed":false,"preventRender":false,"isCompanyIp":false},"pub":{"paper":{"abstract":"\u003Ctitle content-type=\"main\"\u003EAbstract Several classes of arylphosphorus acid amides have been tested in reactions with alkali metal solutions in liquid ammonia. The outcomes of such reactions depend on the structures of the starting materials. Generally, two processes - Birch reduction or cleavage of the P-aryl bond - can be operative. Diarylphosphinic amides tend to undergo double Birch reduction to afford bis(cyclohexadienyl)phosphinic amides.","abstract_zh":"","authors":[{"id":"53f385b0dabfae4b34a1151d","name":"marek stankevic","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"},{"id":"6327463ca95e4d1d0556e3cf","name":"adam wlodarczyk","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"},{"id":"56106d4945ce1e59621ff6c7","name":"damian nieckarz","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"}],"doi":"10.1002\u002Fejoc.201300344","id":"56d8effadabfae2eee6ef033","is_downvoted":false,"is_starring":false,"is_upvoted":false,"issn":"1434-193X","keywords":["Synthetic methods","Organophosphorus chemistry","Phosphorus","Reduction"],"labels":["en_journal"],"lang":"en","num_citation":12,"num_starred":0,"num_upvoted":0,"num_viewed":4,"pages":{"end":"4371","start":"4351"},"title":"The Reactivity of Arylphosphorus Acid Amides Under Birch Reduction Conditions","urls":["http:\u002F\u002Fdx.doi.org\u002F10.1002\u002Fejoc.201300344","http:\u002F\u002Fwww.webofknowledge.com\u002F"],"venue":{"info":{"name":"EUROPEAN JOURNAL OF ORGANIC CHEMISTRY"},"issue":"20","volume":"2013"},"venue_hhb_id":"5ea53024edb6e7d53c031bfd","versions":[{"id":"56d8effadabfae2eee6ef033","sid":"2156671476","src":"mag","year":2013},{"id":"5fc78c265016bf8811090ba9","sid":"WOS:000321737700024","src":"wos","vsid":"EUROPEAN JOURNAL OF ORGANIC CHEMISTRY","year":2013},{"id":"6228e6585aee126c0f1747cf","sid":"W2048145781","src":"openalex","vsid":"EUROPEAN JOURNAL OF ORGANIC CHEMISTRY","year":2013},{"id":"6217bed05aee126c0fe1d0c9","sid":"10.1002\u002Fejoc.201300344","src":"crossref","vsid":"EUROPEAN JOURNAL OF ORGANIC CHEMISTRY","year":2013}],"year":2013},"authorsData":[{"id":"53f385b0dabfae4b34a1151d","name":"marek stankevic","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"},{"id":"6327463ca95e4d1d0556e3cf","name":"adam wlodarczyk","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"},{"id":"56106d4945ce1e59621ff6c7","name":"damian nieckarz","org":"Marie Curie Sklodowska Univ, Fac Chem, Dept Organ Chem, PL-20614 Lublin, Poland"}]}}; </script> <script src="https://fileserver.aminer.cn/lib/react-latest/react.production.min.js"></script> <script src="https://fileserver.aminer.cn/lib/react-latest/react-dom.production.min.js"></script> <script>window.__webpack_public_path__ = '/public/';</script><script src="//ssr.aminer.cn/public/umi.071cb567.js"></script> <script src="https://hm.baidu.com/hm.js?dc703135c31ddfba7bcda2d15caab04e"></script> <script src="https://hm.baidu.com/hm.js?789fd650fa0be6a2a064d019d890b87f"></script> <script src="https://hm.baidu.com/hm.js?6b029ce1079ea4976b430cc9965724db"></script> <!-- <script src="https://fileserver.aminer.cn/misc/collect.min.js"></script> --> <script src="https://fileserver.aminer.cn/misc/collect.min.nano.update.js"></script> <!-- GIO --> <script> var _vds = _vds || []; window._vds = _vds; (function () { _vds.push(['setAccountId', 'ae8dfb99e5e4cda1']); (function () { var vds = document.createElement('script'); vds.type = 'text/javascript'; vds.async = true; vds.src = ('https:' == document.location.protocol ? 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