Weiss, Emilio (Naval Medical Research Institute, Bethesda, Md.) and Harry R. Dressler. Properties of quinoxaline oxide-resistant Rickettsia typhi. J. Bacteriol. 83:415-417. 1962.-An effort was made to apply to the Wilmington strain of Rickettsia typhi the observation that in certain strains of rickettsiae and viruses of the psittacosis group quinoxaline oxide resistance is easily obtained and i...

A room-temperature electrochemical strategy for hydrogenation (deuteration) and reverse dehydrogenation of N-heterocycles over a bifunctional MoNi4 electrode is developed, which includes the quinoxaline using H2O as hydrogen source with 80% Faradaic efficiency hydrogen-rich 1,2,3,4-tetrahydroquinoxaline up to 99% yield selectivity. The in situ generated active atom (H*) plausibly involved quino...

In this research, by a simple and modified method, nanoporous of Ni(II) ion loaded Y-type zeolite (NNZ) was designed and applied as a novel highly efficient catalyst for the synthesis of quinoxalines, pyrido[2,3-b]pyrazines, and indolo[2,3-b]quinoxalines 3a-s. These heterocycles were obtained through a one-pot condensation reaction of aryl-1,2-diamines with 1,2-dik...

The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Electrochemical and density functional studies demonstrate that coordination of electrolyte constituents to quinoxalines modulates their electrochemical properties. Quinoxalines are shown to be electrochemically inactive in most electrolytes in propylene carbonate, yet the pred...

In the title compound, C31H30N4O, the central pyrrolidine ring adopts an envelope conformation with the methyl-ene C atom being the flap. The quinoxaline and indane rings are each planar, having r.m.s. deviations of 0.030 and 0.050 Å, respectively. The pyrrolidine ring mean plane forms dihedral angles of 88.25 (1) and 83.76 (1)° with the quinoxaline and indane rings, respectively. Intra-molecul...

A series of nonsymmetrical 2,3-diaminoquinoxaline derivatives prepared straight-forwardly by the C-N coupling between chloro-quinoxaline (2,3-DCQ) and various amino substrates. Synthesized products (4a-z) with excellent purity (1HNMR) without performing flash column chromatography purification. Investigated antibacterial activity selected nine compounds against Gram-positive, Gram-negative bact...

Condensation of o-phenylenediamine with isatine in refluxing glacial acetic acid gives indolo[2,3-b] quinoxaline. This moiety further condensed with n’-(n-Halo aloxy)-3,4-dihydro carbostyril in refluxing acetonitrile using NaI,K2CO3 and TBAB as catalyst gave us desire product. Series of all six analogs are taken for their antibacterial and antipsychotic activity. The entire tested compound show...

The asymmetric unit of the title compound, 2C(8)H(6)N(2)·C(6)H(7)NO·2H(2)O, contains two quinoxaline mol-ecules, one mol-ecule of 3-amino-phenol and two water mol-ecules which are hydrogen bonded to form a two-dimensional polymeric structure. Each of the symmetry-independent quinoxaline mol-ecules forms separate stacks of different symmetry. In one set of stacks, the mol-ecules are related by a...