A convenient two-step one-pot synthesis of alkylthiophosphoramidates derivatives

被引:2
作者
Miao, ZW [1 ]
Fu, H [1 ]
Han, B [1 ]
Chen, Y [1 ]
Zhao, YF [1 ]
机构
[1] Tsing Hua Univ, Sch Life Sci & Engn, Dept Chem, Minist Educ,Key Lab Bioorgan Phosphorous Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
alkylthiophosphoramidates derivatives; amino acid ester; hydrolysis; O-isopropyl phosphorodichloridothioate; P-31 NMR spectroscopy;
D O I
10.1080/10426500210257
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
N-thiophosphonylamino groups have been greatly overlooked as potentially potent, transition-state analogues, or tetrahedral-intermediate inhibitors of metalloproteases. Alkylthiophosphoramidates derivatives were synthesized by reaction of O-isopropyl phosphorodichloridothioate with an amino acid ester followed by hydrolysis in 2M NH4OH. The reaction was monitored by P-31 NMR spectroscopy.
引用
收藏
页码:641 / 646
页数:6
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