Mn(III)-mediated phosphonation-azidation of alkenes: a facile synthesis of beta-azidophosphonates

Mn(III)-mediated phosphonation-azidation of alkenes: a facile synthesis of beta-azidophosphonates
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Mn(III) 介导的烯烃磷酸化-叠氮化反应:β-叠氮膦酸酯的简便合成

DOI:
10.1039/c5cc03995a
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发表时间:
2015
影响因子:
4.9
通讯作者:
Zhao Yufen
Zhao Yufen
中科院分区:
化学2区
文献类型:
--
作者:
Xu Jian;Li Xueqin;Gao Yuzhen;Zhang Liangliang;Chen Weizhu;Fang Hua;Tang Guo;Zhao Yufen

文献摘要

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通过Mn(OAc)3介导的烯烃自由基氧化膦酸-叠氮化反应,实现了一种合成β-叠氮膦酸酯的新方法。P(O)-H化合物、烯烃和叠氮基三甲基硅烷的起始原料稳定且廉价。这种方法可以很容易地适用于大规模制备。
A new and general method for the synthesis of β-azidophosphonates has been achieved through Mn(OAc)3-mediated radical oxidative phosphonation–azidation of alkenes. The starting materials of P(O)–H compounds, alkenes, and azidotrimethylsilane are stable and cheap. This method can be easily adapted for large-scale preparation.