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Katsuyoshi Shibata

Bio: Katsuyoshi Shibata is an academic researcher from Gifu University. The author has contributed to research in topics: Trifluoromethyl & Silica gel. The author has an hindex of 18, co-authored 156 publications receiving 1156 citations.


Papers
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TL;DR: The reaction of trifluoroacetaldehyde ethyl hemiacetal or hydrate with an equimolar amount of enamines, derived from various methyl ketones, smoothly proceeded to give the corresponding beta-hydroxy-beta-trifluoromethyl ketones in high yields.
Abstract: The reaction of trifluoroacetaldehyde ethyl hemiacetal or hydrate with an equimolar amount of enamines, derived from various methyl ketones, smoothly proceeded to give the corresponding β-hydroxy-β-trifluoromethyl ketones in high yields. An equimolar amount of imines derived from various methyl ketones with aliphatic, aromatic, and heteroaromatic substituents also readily reacted with trifluoroacetaldehyde ethyl hemiacetal or hydrate to afford the corresponding β-hydroxy-β-trifluoromethyl ketones in good to excellent yields. Difluoroacetaldehyde ethyl hemiacetal as well as pentafluoropropionaldehyde also participated in the reaction, affording good yields of the corresponding β-hydroxy-β-difluoromethyl or β-pentafluoropropyl ketones.

36 citations

Journal ArticleDOI
TL;DR: In this paper, 1-Aryl-4, 4,4,4-trifluoro-1,3-butanediones react with β-amino-β-arylacrylonitrile 2, readily available from acetonitrile with aryl nitriles in the presence of potassium t-butoxide, to afford the corresponding 2,6-diaryl-3-cyano-4-(triffluoromethyl)pyridines 3 in moderate to excellent yields.

32 citations

Journal ArticleDOI
TL;DR: Ferrocenyl-substituted 3-cyano-2-methylpyridines were easily prepared by the sonication of α,β-unsaturated carbonyl compounds substituted by ferrocenes in acetonitrile in the presence of potassium t-butoxide as mentioned in this paper.
Abstract: Ferrocenyl-substituted 3-cyano-2-methylpyridines were easily prepared by the sonication of α,β-unsaturated carbonyl compounds substituted by ferrocenes in acetonitrile in the presence of potassium t-butoxide.

32 citations

Journal ArticleDOI
TL;DR: In this article, negative solvatochromism in neutral azo ======¯¯¯¯¯¯dyes containing both strongly electron-donating bis(dialkylamino)thiazolyl and electron-withdrawing 4-(trifluoromethylsulfonyl)phenyl or 2-thiazophosphoric acid 2.

30 citations


Cited by
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1,365 citations

Journal ArticleDOI
TL;DR: Organic fluorine compounds have received a great deal of interest and attention from the scientists involved in diverse fields of science and technology and not only C-F bond formation but also selective C-f bond activation have become current subjects of active investigation from the viewpoint of effective synthesis of fluoroorganic compounds.
Abstract: Fluorine has received great attention in all fields of science. “Small atom with a big ego” was the title of the Symposium at the ACS meeting in San Francisco in 2000, where a number of the current scientific and industrial aspects of fluorine chemistry made possible by the small size and high electronegativity of the atom were discussed. This small atom has provided mankind with significant benefits in special products such as poly(tetrafluroethylene) (PTFE), freon, fluoro-liquid crystals, optical fiber, pharmaceutical and agrochemical compounds, and so on, all of which have their own unique properties that are otherwise difficult to obtain.1 For instance, at present, up to 30% of agrochemicals and 10% of pharmaceuticals currently used contain fluorine atoms. Therefore, organic fluorine compounds have received a great deal of interest and attention from the scientists involved in diverse fields of science and technology. Now, not only C-F bond formation but also selective C-F bond activation have become current subjects of active investigation from the viewpoint of effective synthesis of fluoroorganic compounds. The former is highlighted by designing a sophisticated fluorinating reagent for regioand stereocontrolled fluorination and developing versatile multifunctional and easily prepared building blocks. C-F bond formation has been treated extensively in several reviews2 and books.3 The latter is a subject that has been less explored but would be promising for selective defluorination of aliphatic fluorides, cross-coupling with aryl fluorides, and * To whom correspondence should be addressed. Phone: 81-78-803-5799. Fax: 81-78-803-5799. E-mail: amii@kobe-u.ac.jp and uneyamak@cc.okayamau.ac.jp. † Kobe University. ‡ Okayama University. Chem. Rev. 2009, 109, 2119–2183 2119

1,132 citations

Journal ArticleDOI
TL;DR: In this article, the background information of dye molecules and dye waste characteristics are described and the methods for color measurements and standards are discussed, and different techniques including almost all the known physical, chemical and biological techniques are described for decolorization.
Abstract: The public demand for color-free waste discharge to receiving waters and tougher color standards have made decolorization of a variety of industrial wastes a top priority. Unfortunately, with the complicated color-causing compounds, the decolorization of these wastes is a difficult and challenging task. This article first describes the background information of dye molecules and dye waste characteristics. The methods for color measurements and standards are then discussed. Different techniques including almost all the known physical, chemical and biological techniques are described for decolorization. Each process alone may not be able to meet the requirements. A combination of these processes, for example, chemical-biological, biological-chemical, chemical-physical, chemical-chemical, etc. is often used. The formation of intermediates during the decolorization process is emphasized. These byproducts may be more toxic than the parent compounds. Thus, the extent of the mineralization in waste decolorizatio...

964 citations

Journal ArticleDOI
TL;DR: This poster presents a probabilistic analysis of the response of Na6(CO3)(SO4)(SO3) to Na2SO4 using a high-resolution X-ray diffraction analysis for the stationary phase.
Abstract: Department of Chemistry, Tianjin University, Tianjin 300072, China; Department of Applied Chemistry, China Agricultural University, Beijing 100193, China; UMR 6014 CNRS, Laboratoire COBRA de l’IRCOF, Université et INSA de Rouen, Rue Tesniere, F-76130 Mont Saint Aignan, France; and Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Science, Shanghai 200032, China

851 citations