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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 300-87-8, name is 3,5-Dimethylisoxazole, introducing its new discovery. Formula: C5H7NO

This invention relates to the use of azabicyclic compounds for the treatment of diseases caused by malfunctioning of the nicotinic cholinergic system. These diseases treated include obesity, Parkinson”s disease, anxiety, and ulcerative colitis.

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3,5-Disubstituted isoxazole derivatives, when irradiated in the presence of pentacarbonyliron and water undergo reductive cleavage of the N-O bond to give beta-aminoenones in good yields.

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The invention relates to a process for the preparation of 6, 8 – dioxo – 2 – aza-bicyclo [3, 2, 1] Oct – 2 – ene derivatives, to alkyne amide and substituted isoxazole and water as raw materials, the presence of acid, through the [5 + 2] cycloaddition construction to obtain. Alkyne amide can be by a simple alkyne, paratoluene sulfonyl chloride and benzylamine to synthesize, and follow-up of the cycloaddition reaction operation is simple, quick reaction, does not need to perform multi-step reaction. (by machine translation)

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The theoretical and computational analysis of two isoxazole derivatives 3,5-dimethylisoxazole and 4-chloromethyl-3,5-dimethylisoxazole were carried out along with some of the experimental evidences. The density functional theory calculations of these compounds were done with DFT/B3LYP/6-31+G(d,p) basis set using Gaussian 09 software. From the DFT calculations, the optimization geometry, vibrational analysis, electronic properties, local reactivity descriptors, natural bond orbitals, and other structural properties of the title compounds were elucidated. The chemical shifts of every C and H atom of the title compounds were calculated using Gauge Independent Atomic orbitals (GIAO) method for both proton and carbon NMR spectra. The molecular electrostatic potential of DMI has been found out and the difference in MEP on addition of chloromethyl group is also discussed. The hyperpolarizability calculations of the investigated molecules shows that the nonlinear optical activity of CDMI is greater when compared to DMI.

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Rh2(S-DOSP)4-catalyzed decomposition of heteroaryldiazoacetates in the presence of styrene results in highly diastereoselective and enantioselective cyclopropanations. Heteroaryldiazoacetates containing both electron-rich and electron-deficient heterocycles, such as thiophene, furan, pyridine, indole, oxazole, isoxazole, and benzoxazole, are effective in this chemistry. These studies broaden the range of diazo compounds containing both electron-withdrawing and electron-donating groups, which undergo highly diastereoselective cyclopropanations.

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The new anticonvulsant N-(5′-methylisoxazol-3-yl)-2,6-dimethylbeazamide (D2916), which presents two kinds of methyl groups which could be oxidized, was submitted to various chemical oxidizing agents. Several sites and degrees of oxidation were observed. The main oxidized site was the arylmethyl group without cleavage of the isoxazole ring, leading via carboxylic acid and primary alcohol intermediates to phthalimide and lactame derivatives. In no case was the methyl group of the isoxazole moiety hydroxylated.

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Flash vacuum pyrolysis (FVP) of some 5-alkyl-3-methyl-4-nitroisoxasoles affords 1-nitro-1-cyanoacetone as the only product.A general mechanism is suggested which involves isomerization of the isoxazole to a 1-azirine.A nonclassical reaction of 3-methyl-4-nitroisoxazoles is assumed as a consequence of the electron-withdrawing ability of the nitro group, which precludes ring closure of the nitrile ylide intermediate to the oxazole isomer.The formation of 1-nitro-1-cyanoacetone by FVP of the 3-unsubstituted 5-methyl-4-nitroisoxazole suggests that the activation barrier for a 1,2-hydrogen shift from a 1-azirine or vinylnitrene is lower than that for the formation of nitrile ylide.The FVP of 5-ethyl-3-methylisoxzaole affords 5-ethyl-2-methyloxazole.

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Substituted amides ester and optionally including internal electron donor having electron donor component procatalyst composition disclosure in the nanometer range. A Ziegler – Natta procatalyst composition of the present invention improved catalytic activity and/or improved catalyst (Ziegler non-Natta) catalyst composition and exhibits a selectivity, propylene olefin substrate – wide has a molecular weight distribution is defined. (by machine translation)

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The synthesis of three new isoxazolytnaphthoquinones with an ethyl group on the isoxazole ring is reported.

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Bromodomains recognize and bind acetyl-lysine residues present in histone and non-histone proteins in a specific manner. In the last decade they have raised as attractive targets for drug discovery because the miss-regulation of human bromodomains was discovered to be involved in the development of a large spectrum of diseases. However, targeting eukaryotic pathogens bromodomains continues to be almost unexplored. We and others have reported the essentiality of diverse bromodo-main-containing proteins in protozoa, offering a new opportunity for the development of antiparasitic drugs, especially for Trypansoma cruzi, the causative agent of Chagas? disease. Mammalian bromodomains were classified in eight groups based on sequence similarity but parasitic bromodomains are very divergent proteins and are hard to assign them to any of these groups, suggesting that selective inhibitors can be obtained. In this review, we describe the importance of lysine acetylation and bromodomains in T. cruzi as well as the current knowledge on mammalian bromodomains. Also, we summarize the myriad of small-molecules under study to treat different pathologies and which of them have been tested in trypanosomatids and other protozoa. All the information available led us to propose that T. cruzi bromodomains should be considered as important potential targets and the search for small-molecules to inhibit them should be empowered.

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Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem