M
Masanori Yoshida
Researcher at Hokkaido University
Publications - 63
Citations - 812
Masanori Yoshida is an academic researcher from Hokkaido University. The author has contributed to research in topics: Michael reaction & Catalysis. The author has an hindex of 20, co-authored 62 publications receiving 768 citations.
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α-Fluorination of β-dicarbonyl compounds using p-iodotoluene difluoride under neutral conditions
TL;DR: A selective introduction of a fluorine atom into the α-position of β-dicarbonyl compounds was achieved using p-iodotoluene difluoride under mild conditions and monofluorinated β-ketoesters, ketoamides, and diketones selectively.
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Stereo- and regioselective synthesis of (E,E)-δ-fluoro-α,β,γ,δ-unsaturated carbonyl compounds by Heck-type reaction of fluoroalkenyliodonium salts
TL;DR: In this article, the synthesis of the fluorinated analogue of a biologically active unsaturated fatty acid was also achieved using a Heck-type reaction of (E,E )-2-fluoro-1-iodo-1 -alkenyliodonium salts with α,β-unsaturated carbonyl compounds.
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An Efficient Stereoselective Synthesis of (E)-β-Fluoroalkenyliodonium Salts
TL;DR: In this article, the stereoselective synthesis of (E)-β- fluoroalkenyliodonium salts was performed by the treatment of alk-1-ynes with p-iodotoluene difluoride in the presence of HBF4- Et2O.
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Organocatalytic asymmetric thio-Michael addition of arylmethyl mercaptans to cyclic enones by a primary amino acid
TL;DR: In this article, a simple primary amino acid was found to be an efficient catalyst for the thio-Michael addition of benzyl mercaptan to cyclic enones, which was used for the first time.
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Regio- and stereoselective synthesis of fluoroalkenes and fluoroalkadienes
TL;DR: In this paper, (E)-Fluoroalkenes and (E,E)-fluoroalkadienes are synthesized stereoselectively from 2-fluoro-1-iodoalk-1enes by Pd-catalyzed cross-coupling reaction with organoboranes.