Synthesis of 1- and 2-Piperidinophenazine Derivatives
暂无分享,去创建一个
A number of new piperidinophenazines have been prepared by the reactions of various halogenophenazines and their oxides, including several new compounds, with piperidine. The halogenactivating effect of the oxide groups in 1- or 2-halogenophenazine oxides, which had previously been known, was also observed in the present piperidination. It has been found that 1-chlorophenazine was considerably less reactive than 2-chlorophenazine in the piperidination, that but the 5-oxide group in 1-chlorophenazine-5-oxide enhanced the reactivity of chlorine.
[1] I. J. Pachter,et al. The Wohl—Aue Reaction. II. Reactivities of the Chlorophenazines and their Oxides1 , 1952 .
[2] D. L. Vivian. The Halogen-activating Effect of the N-Oxide Group in Chlorophenazine-N-oxides. Synthesis of an Isomer of Iodinin , 1951 .
[3] J. Hartwell,et al. DIRECT RING CLOSURE THROUGH THE NITRO GROUP. ISOMER FORMATION IN THE SYNTHESIS OF UNSYMMETRICAL PHENAZINES, AND SOME GENERAL OBSERVATIONS ON THE PHENAZINE SYNTHESES , 1951 .