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Masahito Ochiai

Researcher at University of Tokushima

Publications -  305
Citations -  6295

Masahito Ochiai is an academic researcher from University of Tokushima. The author has contributed to research in topics: Hypervalent molecule & Nucleophile. The author has an hindex of 42, co-authored 304 publications receiving 5950 citations. Previous affiliations of Masahito Ochiai include Tokushima Bunri University & Osaka University.

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Iodobenzene-catalyzed alpha-acetoxylation of ketones. in situ generation of hypervalent (diacyloxyiodo)benzenes using m-chloroperbenzoic acid.

TL;DR: It is found that when the reaction was carried out in the absence of a catalytic amount of iodobenzene, Baeyer-Villiger oxidation of a ketone took place, and it is noted that use of water and BF3.Et2O is crucial to the success of this alpha-acetoxylation.
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New C-4-chiral 1,3-thiazolidine-2-thiones: excellent chiral auxiliaries for highly diastereo-controlled aldol-type reactions of acetic acid and .alpha.,.beta.-unsaturated aldehydes

TL;DR: Synthese d'hydroxy-3' alcene-4' oyl-3 alkyl-4 thiazolidinethiones-2 par reaction d'acetyl- 3 alkyl-2 alkl-3 naphroxymethyl-1 piperidine as mentioned in this paper avec des enaldehydes en presence of triflate d'etain II and d'ethyl-ethyl- 1piperidine
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X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

TL;DR: The structures and relative stereochemistries of recaglamide, a novel antileukemic 1H-cyclopenta[b]benzofuran isolated from Aglaia elliptifolia, and dehydrorocaglamides, derived from rocaglide, have been established from spectral and single-crystal X-ray analysis as discussed by the authors.
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Reactions of vinylsilanes with lewis acid-activated iodosylbenzene: stereospecific syntheses of vinyliodonium tetrafluoroborates and their reactions as highly activated vinyl halides

TL;DR: In this paper, a ligand coupling mechanism via the formation of 10-I-3 intermediate 27 containing a copper(III) ligand is proposed for the substitutions of 3 with nucleophiles.