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Sotaro Miyano

Researcher at Tohoku University

Publications -  273
Citations -  6170

Sotaro Miyano is an academic researcher from Tohoku University. The author has contributed to research in topics: Nucleophilic aromatic substitution & Enantioselective synthesis. The author has an hindex of 36, co-authored 273 publications receiving 5927 citations. Previous affiliations of Sotaro Miyano include Ishinomaki Senshu University & Toyohashi University of Technology.

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Facile synthesis of p-tert-butylthiacalix[4]arene by the reaction of p-tert-butylphenol with elemental sulfur in the presence of a base

TL;DR: In this article, the four methylene bridges of p-tert-butylcalix[4]arene are replaced by sulfide linkages, which can be easily synthesized in a single step (54%) by heating a mixture of ptertbutylphenol, elemental sulfur S8 and NaOH in tetraethylene glycol dimethyl ether with concomitant removal of the resulting hydrogen sulfide.
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Ruthenium Complex-Catalyzed Direct Ortho Arylation and Alkenylation of 2-Arylpyridines with Organic Halides

TL;DR: The ortho position of the aromatic ring of imino group substituted aromatic compounds is directly arylated and alkenylated with organic halides in the presence of a catalytic amount of a ruthenium(II)-phosphine complex.
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Synthesis of p-tert-butylthiacalix[4]arene and its inclusion property

TL;DR: In this paper, a practical method for the synthesis of p-tert-butylthiacalix[4]arene (TC4A), in which the methylene bridges of C4A are replaced by epithio groups, is presented by heating a mixture of ptert butylphenol, elemental sulfur S8, and NaOH as a base catalyst in tetraethylene glycol dimethyl ether.
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Can Thiacalixarene Surpass Calixarene

TL;DR: In this paper, the authors present the results of their own study to demonstrate the potentials over the limits of the conventional calixarenes, putting emphasis on the indispensable role of the bridging sulfur.
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Selective oxidation of thiacalix[4]arenes to the sulfinyl- and sulfonylcalix[4]arenes and their coordination ability to metal ions

TL;DR: In this paper, the four methylene birdge of calix[4]arenes are replaced by sulfide linkages, and they were selectively oxidized to sulfinyl- or sulfonylcalix[ 4]arene under mild conditions with control of the stoichiometry of the oxidant.