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Fuyuhiko Inagaki

Researcher at Kobe Gakuin University

Publications -  85
Citations -  1503

Fuyuhiko Inagaki is an academic researcher from Kobe Gakuin University. The author has contributed to research in topics: Cycloaddition & Catalysis. The author has an hindex of 24, co-authored 85 publications receiving 1371 citations. Previous affiliations of Fuyuhiko Inagaki include Stanford University & Kanazawa University.

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Air-stable cationic gold(I) catalyst featuring a Z-type ligand: promoting enyne cyclizations.

TL;DR: An enyne cyclization in the presence of either [Au→B](+) or[Au](+) showed that [Ae→B]-(+) promotes the reactivity, which enabled the effective construction of not only five- and six-membered rings, but also seven- Membered rings.
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[2+2+1] Cyclization of allenes

TL;DR: This review focuses on the origin and progress of the allenic [2+2+1] cyclocarbonylation, including the chirality transfer of theallene and its synthetic applications.
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Rhodium(I)‐Catalyzed Intramolecular [5+2] Cycloaddition Reactions of Alkynes and Allenylcyclopropanes: Construction of Bicyclo[5.4.0]undecatrienes and Bicyclo[5.5.0]dodecatrienes

TL;DR: Highly strained cyclopropane derivatives have served as useful and powerful C3 building blocks for the construction of various ring systems, and the metal-catalyzed cleavage of the activated carbon-carbon s bond of the cycloprostane ring 3] must be one of the most attractive methods from a synthetic point of view.
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Rhodium(I)-Catalyzed Intramolecular Carbonylative [2+2+1] Cycloaddition of Bis(allene)s: Bicyclo[6.3.0]undecadienones and Bicyclo[5.3.0]decadienones

TL;DR: The title reaction makes it easy to construct the bicyclo[6.3.0]undecadienone framework in high yields (see scheme) and a template effect is not required to achieve this ring-closing reaction efficiently.
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Rhodium(I)-catalyzed intramolecular pauson-khand-type [2 + 2 + 1] cycloaddition of allenenes.

TL;DR: This method provides a new procedure for the construction of the bicyclo[4.3.0]non-1(9)-en-8-one skeleton having an alkyl appendage at the ring juncture, which was hardly attained in a satisfactory yield by the Pauson-Khand reaction of the corresponding enynes.