Tosoh Organic Chemical Co.

Yamaguchi-shi, Japan

Tosoh Organic Chemical Co.

Yamaguchi-shi, Japan
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Eguchi H.,Tosoh Organic Chemical Co. | Nishiyama M.,Tosoh Corporation | Ishikawa S.-I.,Tosoh Corporation | Soga S.-I.,Tosoh Organic Chemical Co. | Koie Y.,Tosoh Corporation
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry | Year: 2012

Ttransition-metal catalyzed cross-coupling reactions (C-C, C-N) are the useful and powerful tools for the synthesis of OLED (organic light emitting diode) or LCD (liquid crystal display) materials. For many years, a major drawback of this reaction has been the poor reactivity of aryl chloride, which are more attractive in terms of cost and availability than the corresponding bromide, iodide and triflate. This review summarized the recent developments combined with our work utilizing the aryl chloride in this area.


Kanazawa Y.,Tottori University | Yokota T.,Tottori University | Ogasa H.,Tottori University | Watanabe H.,Nihon University | And 3 more authors.
Tetrahedron | Year: 2015

We report the chemoselective amination of bromoiodobenzenes with diarylamines by palladium/Xantphos or a ligand-free copper catalyst. The reactions by these two types of catalysts proceeded with a high chemoselectivity and afforded monobrominated triarylamines in good yields. These products are useful intermediates for the synthesis of unsymmetrical bistriarylamines. © 2015 Elsevier Ltd. All rights reserved.


Kuwano R.,Kyushu University | Matsumoto Y.,Kyushu University | Shige T.,Kyushu University | Tanaka T.,Kyushu University | And 2 more authors.
Synlett | Year: 2010

Bis(ortho-substituted aryl)amines were arylated on the nitrogen atom with various haloarenes in high yields using the palladium catalyst, which was generated from palladium(II) acetate and tri(tert-butyl)phosphine. © Georg Thieme Verlag Stuttgart.


Uoyama H.,Ehime University | Chenxin C.,Ehime University | Chenxin C.,Japan Science and Technology Agency | Tahara H.,Ehime University | And 7 more authors.
Heterocycles | Year: 2010

4,11-Ethano-4,11-dihydro-2H-anthra[2,3-c]pyrrole and 4,11-ethano-4,11- dihydroanthra[2,3-c]thiophene derivatives were prepared from the corresponding bicyclo[2.2.2]octadiene-fused five-membered heterocycles by the Diels-Alder reaction with in situ generated α,α′-dibromo-o-xylylene derivatives. Their thermogravimetric analyses showed evapolation without formation of 2H-anthra[2,3-c]pyrrole and anthra[2,3-c]thiophene derivatives under the atmospheric pressure. © 2010 The Japan Institute of Heterocyclic Chemistry Received.


Matsuoka H.,Kyoto University | Hachisuka M.,Kyoto University | Uda K.,Kyoto University | Onishi T.,Kyoto University | Ozoe S.,Tosoh Organic Chemical Company
Chemistry Letters | Year: 2012

Ionic amphiphilic diblock copolymers, such as polystyreneb- poly(styrenesulfonate), show non-surface activity when some requirements are satisfied. The main origin of this unique property has been thought to be an image charge repulsion at the air/water interface. In this study, surface activity/non-activity was examined for random copolymers in addition to homopolymers. Random copolymers of styrene and styrenesulfonate were found to be surface active, while the poly(styrenesulfonate) homopolymer was slightly surface active. This observation cannot be interpreted by image charge repulsion alone since these are all polyanions and the block copolymer is mostly hydrophobic. Stable polymer micelle formation in the block copolymer system is also an essential origin of non-surface activity. © 2012 The Chemical Society of Japan.


Provided are high purity sodium p-styrenesulfonate with an excellent hue which is useful as a reactive emulsifier or dispersant for producing a polymer emulsion, or synthetic starch for clothing ironing and poly(sodium p-styrene-sulfonate) with an excellent hue using the same or sodium p-styrenesulfonate improved in fluidity while keeping good solubility. An aqueous p--bromoethylbenzenesulfonic acid solution and an aqueous sodium hydroxide solution are reacted under specific conditions to control the particle size, thereby obtaining sodium p-styrenesulfonate particles improved in a balance between fluidity and solubility, and further, impurities such as isomers are reduced, thereby obtaining high-purity sodium p-styrenesulfonate with an excellent hue.


Provided are: a polymer-supported phosphane compound exhibiting excellent catalytic reaction activity; a complex including the compound and a transition metal; and a catalyst including the complex. This polymer compound includes: units of threefold styrene cross-linked phosphane; and styrene units having substituent groups (R) in position 4 (provided that R represents hydrogen, a C1-6 lower alkyl group, a C1-6 lower alkoxy group, or a polar functional group). In the formula in which the polymer compound includes structure (1), PS represents a polystyrene unit chain including the styrene units having the substituent groups (R). The complex includes the polymer and a transition metal. The catalyst for an organic compound coupling reaction includes the complex.

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