Abstract:
The novel compound 3,3-Dinitro-4,4′-hydrozofurazan and the methods of preparation. The method of preparation 3,3-Dinitro-4,4′-hydrazofurazan which comprises partially reducing 3,3′-Dinitro-4,4′-azoxyfurazan. The method of preparing 3,3′-Dinitro-4,4′-hydrazofurazan by the partial reduction of 3,3′-Dinitro-4,4′-azofurazan.
Abstract:
An efficient direct functionalization of nitrocubanes has been achieved byrradiation of a solution in an oxalyl halide to yield halogenated and halocarbonylated derivatives of nitrocubanes.
Abstract:
This invention consists of a method for converting diaminoglyoxime to diaminofurazan that can be carried out efficiently at about atmospheric pressure without the need for high pressure containment apparatus.This invention also consists of a method which comprises converting diaminoglyoxime to diaminofurazan at about atmospheric pressure in the presence of a strong base and/or an organic polar solvent.
Abstract:
The disclosure describes photochemical synthesis of halogenated polycarboxycubanes from simple carboxycubanes and an oxalyl halide. It is possible to synthesize 6-Chloro-1,2,4,7-tetracarbomethoxycubane and 2-Chloro-1,3,5,7-tetracarbomethoxycubane. Photochemical synthesis of halogenated polycarboxycubanes from carboxy cubane and an oxalyl halide is reported.
Abstract:
A process for selective, direct oxidation of amine or amine hydrochloride mpounds is described. It uses mixed oxidizing agents of monopersulfate and ozone.
Abstract:
The present invention is directed to the synthesis of useful products from the explosive trinitrotoluene. This substance has a limited shelf life as a reliable explosive and large quantities of it have and will become surplus. Ecologically safe, and preferably commercially useful ways of disposing of it are therefore much to be desired. In the present invention the end products are nitroindoles of the general formula 4-Z.sup.1,6-Z.sup.2 indole wherein Z.sup.1 and Z.sup.2 are the same or different and are halo or nitro provided at least one of said groups is nitro.
Abstract:
An efficient direct functionalization of nitrocubanes has been achieved byrradiation of a solution in an oxalyl halide to yield halogenated and halocarbonylated derivatives of nitrocubanes.
Abstract:
An efficient direct functionalization of nitrocubanes has been achieved by irradiation of a solution in an oxalyl halide to yield halogenated and halocarbonylated derivatives of nitrocubanes.
Abstract:
An efficient direct functionalization of nitrocubanes has been achieved by irradiation of a solution in an oxalyl halide to yield halogenated and halocarbonylated derivatives of nitrocubanes.
Abstract:
An efficient direct functionalization of nitrocubanes has been achieved byrradiation of a solution in an oxalyl halide to yield halogenated and halocarbonylated derivatives of nitrocubanes.