Results 171 to 180 of about 5,992 (210)
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Hydrogen bonding in thiosemicarbazide

Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1970
In a recent paper (Domiano, Fava Gasparri, Nardelli & Sgarabotto, 1969, DGNS) the crystal-structure analysis of thiosemicarbazide, carried out by photographic methods, was reported (final R=9 .9%) . The positions of the hydrogen atoms were postulated from consideration of the hybridization of the nitrogen atoms and the packing interactions, no direct ...
G. D. Andreetti   +4 more
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A reinvestigation of the cyclodesulfurization of thiosemicarbazides

Journal of Heterocyclic Chemistry, 1981
AbstractA recent report describing the preparation of 2‐(substituted‐amino)‐3,4‐dihydro‐5H‐1,3,4‐benzotriazepin‐5‐ones (3), by the cyclodesulfurization of hydrazides prepared from o‐aminobenzoylhydrazine (1) and isothiocyanates, is erroneus. The products resulting from this reaction sequence are, instead, 2‐(substituted‐amino)‐5‐(o‐aminophenyl)‐1,3,4 ...
Shyam Sunder   +2 more
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Susceptibility to audiogenic seizure induced by thiosemicarbazide

Experimental Neurology, 1969
Abstract Rats, cats, and monkeys were subjected to audiogenic stimuli after the administration of thiosemicarbazide (TSC). The treated rats responded to audiogenic stimulation with episodic running behavior (ERB) with or without convulsion (C), the most effective dosage being 4.4 mg/kg.
J A, Wada, T, Asakura
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Menthone Semicarbazides and Thiosemicarbazides as Anticonvulsant Agents

Medicinal Chemistry, 2010
A series of novel (+/-) 3-menthone semi carbazides (1-7) and thiosemicarbazides synthesized using an appropriate synthetic route and characterized by thin layer chromatography and spectral analysis. The anticonvulsant activity of synthesized compounds was established after intraperitoneal administration in three seizure models in mice which include ...
Jainendra, Jain   +3 more
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Oscillating chemiluminescence with thiosemicarbazide in a batch reactor

Luminescence, 2008
AbstractOscillating chemical reactions are complex systems involving a large number of chemical species. In oscillating chemical reactions, some species, usually reaction intermediates, exhibit fluctuations in their concentration. In this report, a novel slowly‐damped oscillating chemiluminescence produced by the addition of thiosemicarbazide (TSC) to ...
M H, Sorouraddin, M, Iranifam
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Laser Desorption and Ionization of Thiosemicarbazides

Colloid Journal, 2020
Ionized products of desorption of thiosemicarbazides from a steel target surface before and after deposition of solid solutions of thiosemicarbazides in organic matrices (nicotinic acid, α-cyano-4-hydroxycinnamic acid, 2,5-dihydroxybenzoic acid, and dithranol) onto it have been studied by mass spectrometry.
I. A. Polunina   +2 more
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Structure of 4-(3-chlorophenyl)thiosemicarbazide

Acta Crystallographica Section C Crystal Structure Communications, 1991
C7H8ClN3S, Mr = 201.67, monoclinic, P21/c, a = 6.914 (5), b = 4.304 (4), c = 30.306 (3) A, beta = 94.66 (3) degrees, V = 899.0 (1) A3, Z = 4, Dm = 1.54, Dx = 1.490 Mg m-3, lambda (Cu K alpha) = 1.5418 A, mu = 5.54 mm-1, F(000) = 416, T = 298 K, final R = 0.048 for 1219 observed reflections.
D, Chattopadhyay   +4 more
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ChemInform Abstract: Thiosemicarbazides in Heterocyclization

ChemInform, 2011
AbstractReview: 142 refs.
Alaa A. Hassan, Ahmed M. Shawky
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Computational studies of the cyclization of thiosemicarbazides

Journal of Physical Organic Chemistry, 2007
AbstractWhile typically cyclodehydration of thiosemicarbazides in acidic media leads to 1,3,4‐thiadiazoles, we have recently shown that under reflux conditions in anhydrous acetic acid the cyclization yields an imidazolidine derivative. The mechanism of this reaction has been characterized theoretically.
Agata Siwek, Piotr Paneth
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A review on development of bio-active thiosemicarbazide derivatives: Recent advances

Journal of Molecular Structure, 2021
Dhaval B Patel, Hitesh D Patel
exaly  

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