Nitrosyl‐selensäure

Meyer, Julius; Wagner, Walter

doi:10.1002/cber.19220550314

Cited by 14 publications

(15 citation statements)

References 2 publications

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“…The substance was prepared by a method given by Meyer (1924). It was recrystallized from saturated solutions in nitric acid by cooling or from solutions in acetone by slow evaporation.…”

Section: Methodsmentioning

confidence: 99%

The crystal and molecular structure of hydroxyquinones and salts of hydroxyquinones. V. Hydronium nitranilate, nitranilic acid hexahydrate

Andersen¹

1967

Acta Cryst

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The structure of nitranilic acid hexahydrate has been determined by use of partial three-dimensional data. The cell dimensions are: a= 3-657, b= 19.399, c= 9"184/~, B=94.28 °. The space group is P21/c and Z= 2. The geometry of the carbon ring system is similar to that found in chloranilate and nitranilate ions, and the carbon-oxygen bonds are of equal length (1-22 A, the same as in nitranilate). There is thus strong evidence that the substance is hydrated hydronium nitranilate. The ring is planar, but the nitro group is out of the ring plane.

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“…The substance was prepared by a method given by Meyer (1924). It was recrystallized from saturated solutions in nitric acid by cooling or from solutions in acetone by slow evaporation.…”

Section: Methodsmentioning

confidence: 99%

The crystal and molecular structure of hydroxyquinones and salts of hydroxyquinones. V. Hydronium nitranilate, nitranilic acid hexahydrate

Andersen¹

1967

Acta Cryst

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“…Vancomycin and Cefatzine were used as control [34]. The compound 1-(4-Chlorophenyl)-6,7,8,9-tetrahydro-4Hbenzo [4,5]thieno [2,3-d] [1,2,4]triazolo [3,4-b]-pyrimidin-5one ( Fig. 35) displayed a promising antimicrobial activity.…”

Section: September 2018mentioning

confidence: 99%

“…In 1882, Viktor Meyer indicated it to be the first representative of a new ring system by isolating the impurity via its sulfonic acid derivative (Figs. [1][2][3][4][5][6][7][8].…”

Section: Introductionmentioning

confidence: 99%

“…Thiophene, in terms of boiling point and odor, nearly resemble the corresponding benzene compounds and are stable liquids [5]. It is considered as aromatic because the resonance energy of thiophene is about 22-28 kcal/mol, which is less than that of resonance energy of benzene (36 kcal/mol).…”

Section: Introductionmentioning

confidence: 99%

“…The antimicrobial screening of the synthesized compounds was performed by agar diffusion assay using Ampicillin, Streptomycin, and Nystatin as positive controls. Among the synthesized derivatives, 3-amino-2-(phenylamino)-3,5,6,7-tetrahydro-4H-cyclopenta [4,5] thieno [2,3-d] pyrimidin-4-one ( Fig. 9) showed significant activity against Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus subtilis, and Candida albicans [14].…”

Section: Introductionmentioning

confidence: 99%

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Thiophene Scaffold as Prospective Antimicrobial Agent: A Review

Mishra

Sachan

Kumar

et al. 2018

Journal of Heterocyclic Chem

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Thiophene has emerged as a potent scaffold that has pulled the keen interest of the researchers because of its considerable diversity in biological activities. The versatility of the thiophene nucleus is demonstrated by the successful introduction of its derivatives, which have anti‐inflammatory (Thenaldine), anticancer (Ralitrexed), antioxidant (Erdosteine), and antimicrobial (Cefoxitin and Temocillin) activities. This decent variety in the biological response profile has pulled in the consideration of numerous researchers to research this skeleton to its distinctive potential against several activities. This review is integral to prior reviews and plans to review the work regarding antibacterial and antifungal activities of thiophene, substituted thiophene and thiophene‐like compounds, and also Schiff bases of thiophene and substituted thiophenes from year 1995 to the beginning of 2018.

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Syntheses of arsinolipids: non-isosteric analogues of phospholipids

Kordalis¹,

Ioannou²

2000

Appl. Organometal. Chem.

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Reaction of alkaline benzenearsonous and 2,3‐dihydroxypropylarsonous acids with rac‐glycidol affords the corresponding arsinic acids, which after reduction with thiophenol are acylated with either fatty‐acid chlorides/pyridine or fatty acids/dicyclohexylcarbodiimide/4‐dimethylaminopyridine and oxidized with hydrogen peroxide to give the arsinolipids (rac‐2,3‐diacyloxypropyl)phenylarsinic and bis‐(rac‐2,3‐diacyloxypropyl)arsinic acids. The latter is a non‐isosteric analogue of bisphosphatidic acid. Copyright © 2000 John Wiley & Sons, Ltd.

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Nitrosyl‐selensäure

Cited by 14 publications

References 2 publications

The crystal and molecular structure of hydroxyquinones and salts of hydroxyquinones. V. Hydronium nitranilate, nitranilic acid hexahydrate

The crystal and molecular structure of hydroxyquinones and salts of hydroxyquinones. V. Hydronium nitranilate, nitranilic acid hexahydrate

Thiophene Scaffold as Prospective Antimicrobial Agent: A Review

Syntheses of arsinolipids: non-isosteric analogues of phospholipids

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