Results 241 to 250 of about 47,486 (283)
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Acta Crystallographica Section C Crystal Structure Communications, 2002
In beta-phenazine, C(12)H(9)N(2), the molecules show a sandwich herring-bone type of packing. The experimental crystal structure shows very good agreement with that predicted earlier from systematic searches of potential packing arrangements for the known unit cell [Hammond, Roberts, Smith & Docherty (1999). J. Phys. Chem. B, 103, 7762-7770].
Wojciech, Jankowski, Maria, Gdaniec
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In beta-phenazine, C(12)H(9)N(2), the molecules show a sandwich herring-bone type of packing. The experimental crystal structure shows very good agreement with that predicted earlier from systematic searches of potential packing arrangements for the known unit cell [Hammond, Roberts, Smith & Docherty (1999). J. Phys. Chem. B, 103, 7762-7770].
Wojciech, Jankowski, Maria, Gdaniec
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Antitubercular 2,8-bis(alkylaminomethyl)phenazines
Journal of Medicinal Chemistry, 1978The preparation and antitubercular properties of a series of 2,8-bis(alkylaminomethyl)phenazines are described. These compounds all inhibited the growth of Mycobacterium smegmatis ATCC 607 in vitro. 2,8-Bis(dibutylaminomethyl)phenazine (5c) was also active against a lethal Mycobacterium tuberculosis H37Rv infection in mice.
K C, Murdock +3 more
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Electrochemistry communications, 2018
Extracellular electron transfer (EET) is believed to be a bottleneck in microbiologically influenced corrosion (MIC), also known as biocorrosion, by electro-active microbes.
Ye Huang +7 more
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Extracellular electron transfer (EET) is believed to be a bottleneck in microbiologically influenced corrosion (MIC), also known as biocorrosion, by electro-active microbes.
Ye Huang +7 more
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Journal of Heterocyclic Chemistry, 1969
AbstractEleven phenazines were identified as fermentation products of a bacterium. They included the previously unknown 2,9‐dihydroxyphenazine‐1‐carboxyIic acid (4), 1,8‐phenazinediol‐1()‐oxide (5) and 8‐amino‐1‐phenazinol (6) as well as phenazine‐1,6‐dicarboxylic acid (1),9‐hydroxyphena‐zine‐1‐carboxylic acid (2) and 1,8‐phenazinediol (3) not isolated
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AbstractEleven phenazines were identified as fermentation products of a bacterium. They included the previously unknown 2,9‐dihydroxyphenazine‐1‐carboxyIic acid (4), 1,8‐phenazinediol‐1()‐oxide (5) and 8‐amino‐1‐phenazinol (6) as well as phenazine‐1,6‐dicarboxylic acid (1),9‐hydroxyphena‐zine‐1‐carboxylic acid (2) and 1,8‐phenazinediol (3) not isolated
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Journal of the Science of Food and Agriculture, 1969
AbstractThe synthesis of forty‐one phenazines, mono‐substituted with alkyl, alkoxy, alkylthio and alkylsulphonyl groups is described.Phytotoxicity was highest in the alkyl series and both 1‐ and 2‐methylphenazines are highly effective. herbicides.Although several n‐alkyl, branched alkyl and n‐alkoxyphenazines were highly fungicidal and acaricidal, only
B, Cross +3 more
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AbstractThe synthesis of forty‐one phenazines, mono‐substituted with alkyl, alkoxy, alkylthio and alkylsulphonyl groups is described.Phytotoxicity was highest in the alkyl series and both 1‐ and 2‐methylphenazines are highly effective. herbicides.Although several n‐alkyl, branched alkyl and n‐alkoxyphenazines were highly fungicidal and acaricidal, only
B, Cross +3 more
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Biochemical and Biophysical Research Communications - BBRC, 1972
M. Nishikimi, N. Rao, K. Yagi
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M. Nishikimi, N. Rao, K. Yagi
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Phenazine Syntheses. I. Halogen-Substituted Phenazines
The Journal of Organic Chemistry, 1953Donald L. Vivian, Jonathan L. Hartwell
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