Lewis acid-promoted imine synthesis by the insertion of isocyanides into C-H bonds of electron-rich aromatic compounds
The Lewis acid-promoted insertion of isocyanides into aromatic C-H bonds is reported. An imine functionality containing an array of N-substituents can be introduced directly into electron-rich aromatics in good yields.
One-Step Hydroamidation of a Schiff Base with Trichlorosilane
We have found that the treatment of a Schiff base (2) with trichlorosilane and chloroacetyl chloride results in a highly active chloroacetamide herbicide (1) in an excellent yield .This one-step hydroamidation reaction of a Schiff base is a useful synthet
Okamoto, Hidenori,Kato, Shozo
p. 2128 - 2130
(2007/10/02)
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