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作 者:Zheng Jie HE Ju Xiang LIU Zheng Hong ZHOU and Chu Chi TANG(State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071)
出 处:《Chinese Chemical Letters》1998年第10期903-905,共3页中国化学快报(英文版)
摘 要:The isomerization/chlorination of O, O-diallyl thiophosphoric (-nic) acid esters with phosphrus oxychloride gives S-allyl thiophosphoro (-no)chloride, which reacts with subsittuted phenol in chloroform in the presence of triethylamine to afford eighteen new S-allyl thiophosphoric(-nic) acid derivatives. Thus, a new convenient method has been provided for synthesis of the title compounds.The isomerization/chlorination of O, O-diallyl thiophosphoric (-nic) acid esters with phosphrus oxychloride gives S-allyl thiophosphoro (-no)chloride, which reacts with subsittuted phenol in chloroform in the presence of triethylamine to afford eighteen new S-allyl thiophosphoric(-nic) acid derivatives. Thus, a new convenient method has been provided for synthesis of the title compounds.
关 键 词:ISOMERIZATION CHLORINATION phosphoro(-no)thionate phosphoro(-no)thiolate phosphoro (-no) chlorothiolate phosphorus oxychloride
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