Reaction of 2,3-dibromo-3-nitroacrylates with N-amino-N″-nitroguanidine

Russian Journal of Organic Chemistry -     

Exact solutions to magnetogasdynamic equations in Lagrangian coordinates

The Lie group of point transformations, which leave the equations for a simplified model of one dimensional ideal gas in magnetogasdynamics invariant, are used to obtain some exact solutions for the governing system of hyperbolic partial differential equations (PDEs). Similarity variables which reduces the governing system of PDEs into system of ordinary differential equations (ODEs) are determined through the transformations. The resulting ODEs are solved analytically to obtain some exact solutions that exhibits space-time dependence. Further, we study the propagation of weak discontinuity through a state characterized by one of the solutions.     

Comparative theoretical study on the corrosion inhibition properties of benzoxazole and benzothiazole

Research on Chemical Intermediates - The electronic parameters of two azole molecules, namely benzoxazole (BOX) and benzothiazole (BTH), have been studied using DFT/B3LYP, MP2, and HF methods with...     

A Single Enzyme Transforms a Carboxylic Acid into a Nitrile through an Amide Intermediate

The biosynthesis of nitriles is known to occur through specialized pathways involving multiple enzymes; however, in bacterial and archeal biosynthesis of 7‐deazapurines, a single enzyme, ToyM, catalyzes the conversion of the carboxylic acid containing 7‐carboxy‐7‐deazaguanine (CDG) into its corresponding nitrile, 7‐cyano‐7‐deazaguanine (preQ₀). The mechanism of this unusual direct transformation was shown to proceed via the adenylation of CDG, which activates it to form the newly discovered amide intermediate 7‐amido‐7‐deazaguanine (ADG). This is subsequently dehydrated to form the nitrile in a process that consumes a second equivalent of ATP. The authentic amide intermediate is shown to be chemically and kinetically competent. The ability of ToyM to activate two different substrates, an acid and an amide, accounts for this unprecedented one‐enzyme catalysis of nitrile synthesis, and the differential rates of these two half reactions suggest that this catalytic ability is derived from an amide synthetase that gained a new function.     

1,7-difluoro-1,1,3,5,7,7-hexanitro-3,5-diazaheptane: Crystal structure and sensitivity to mechanical actions

The X-ray crystallographic analysis of 1,7-difluoro-1,1,3,5,7,7-hexanitro-3,5-diazaheptane has been carried out. We have also determined its sensitivity to mechanical actions and a set of calculated and experimental data on explosion characteristics.