Title of article :
Hemiacetal and hemiaminal formation at fluoroacyl moiety
Author/Authors :
Masaki Matsui، نويسنده , , Kaede Yamada، نويسنده , , Kazumasa Funabiki، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2005
Abstract :
Hemiacetals and hemiaminals were produced not only at a trifluoroacetyl (CF3CO) moiety but also at difluoroacetyl (CHF2CO) and pentafluoroalkanoyl (C2F5CO) moieties. As larger was the electron-withdrawing nature and less bulky was the fluoroalkyl (Rf) group and smaller was the size of an alcohol, the ratio of hemiacetal form increased. Not only a CF3CO moiety but also monofluoroacetyl (CH2FCO), CHF2CO, and C2F5CO moieties produced the hemiaminals. As larger was the electron-withdrawing nature of Rf group and smaller was an amine, the ratio of hemiaminal form increased.
Keywords :
Perfluoroacyl , Hemiaminal , Steric effect , Electronic effect , Hemiacetal
Journal title :
Tetrahedron
Journal title :
Tetrahedron