Regio- and stereospecific ring opening of 1,1-dialkyl-2-(aryloxymethyl)aziridinium salts by bromide

被引:61
作者
D'hooghe, M
Van Speybroeck, V
Waroquier, M
De Kimpe, N [1 ]
机构
[1] Univ Ghent, Dept Organ Chem, Fac Biosci Engn, Ghent, Belgium
[2] Univ Ghent, Ctr Mol Modeling, Theoret Phys Lab, Ghent, Belgium
关键词
D O I
10.1039/b518298k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enantiomerically pure 2-(aryloxymethyl)aziridines are efficiently transformed into chiral N-(2-bromo-3-aryloxypropyl) amines via a regio- and stereospecific ring opening of the intermediate aziridinium salts, and the experimental results are rationalized on the basis of some high level ab initio calculations.
引用
收藏
页码:1554 / 1556
页数:3
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