Iron-catalyzed synthesis of glycine derivatives via carbon-nitrogen bond cleavage using diazoacetate.
Yoichiro Kuninobu, Mitsumi Nishi, Kazuhiko Takai
Index: Chem. Commun. (Camb.) 46(46) , 8860-2, (2010)
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Abstract
Treatment of tertiary amines with diazoacetate in the presence of a catalytic amount of an iron salt, FeCl(3), in ethanol gave glycine derivatives. In this reaction, a carbon-nitrogen single bond of the amine was cleaved.
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