METHYL PHENYLIMINOMALONATE AND ITS REACTIONS.

RS Curtiss, FGC Spencer

Index: Curtiss; Spencer Journal of the American Chemical Society, 1911 , vol. 33, p. 990

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Abstract

MTe have for some time sought a method of making the above-named compound, C, H, N= C (CO, R),, but without avail. Considered as a dicarboxyl addition product of phenyl isocyanide, C, H, N= C, or as an analog of phenyl isocyanate, C, H, N= C= 0, containing the negative carbomethoxyl groups in place of oxygen, one might predict its chemical properties and behax-ior with some degree of accuracy., 4s Nefl and others have so well shown in ...