M
Masahiro Noji
Researcher at Meiji Pharmaceutical University
Publications - 18
Citations - 620
Masahiro Noji is an academic researcher from Meiji Pharmaceutical University. The author has contributed to research in topics: Catalysis & Trifluoromethanesulfonate. The author has an hindex of 5, co-authored 14 publications receiving 596 citations. Previous affiliations of Masahiro Noji include Hokkaido University.
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Enantioselective synthesis of binaphthol derivatives by oxidative coupling of naphthol derivatives catalyzed by chiral diamine-copper complexes
TL;DR: In this paper, an efficient process of aerobic oxidative coupling of 2-naphthol derivatives catalyzed by 1 mol % of Cu(OH)Cl·TMEDA has been developed.
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Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate
TL;DR: The combination of a secondary benzyl alcohol and a metal triflate in nitromethane was a highly effective secondary-benzylation system and trifluoromethanesulfonic acid (triflic acid, TfOH) was also a good catalyst.
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Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds
TL;DR: The rare earth metal and hafnium triflate-catalyzed secondary benzylation and allylation of 1,3-diketones, ketoesters, and ketoamides are described and the reaction conditions were easily optimized by the selection of catalysts based on the Lewis acidity of the triflates and reaction temperature.
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Photoreactions of β-aziridinylacrylonitriles and acrylates with alkenes: formation of head-to-head adducts and application to the preparation of pyrrolizidine alkaloid
TL;DR: In this article, the photochemical C,C-bond cleavage of N -benzyl β-aziridinylacrylonitrile 1 and acrylate 2 and the subsequent cycloaddition with electron-deficient alkenes afforded head-to-head adducts selectively and efficiently.
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Photoreactions of β-aziridinylacrylonitrile. 1,3-Dipolar cycloadditions of photoinduced azomethine ylide
TL;DR: The photoinduced azomethine ylide A from the 3-(1-benzylaziridin-2-yl)prop-2enenitrile 1 undergoes 1,3-dipolar cycloaddition with electron-deficient olefins to give the head-to-head adducts selectively and efficiently as discussed by the authors.