Y
Yasuo Tanaka
Researcher at Osaka University
Publications - 10
Citations - 1905
Yasuo Tanaka is an academic researcher from Osaka University. The author has contributed to research in topics: Catalysis & Hydrogen bond. The author has an hindex of 7, co-authored 10 publications receiving 1799 citations.
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Journal ArticleDOI
Efficient catalytic addition of aromatic carbon-hydrogen bonds to olefins
Shinji Murai,Fumitoshi Kakiuchi,S. Sekine,Yasuo Tanaka,Asayuki Kamatani,Motohiro Sonoda,Naoto Chatani +6 more
TL;DR: The selective cleavage of carbon-hydrogen bonds in organic compounds is a critical step in many organic syntheses, and is particularly important in the conversion of hydrocarbons to useful organic compounds.
Journal ArticleDOI
Catalytic Addition of Aromatic Carbon–Hydrogen Bonds to Olefins with the Aid of Ruthenium Complexes
Fumitoshi Kakiuchi,S. Sekine,Yasuo Tanaka,Asayuki Kamatani,Motohiro Sonoda,Naoto Chatani,Shinji Murai +6 more
TL;DR: In this paper, the importance of the coordination of the oxygen atom of the ketone to ruthenium and the intervention of a cyclometallation intermediate are suggested. But the results of the deuterium labeling experiment using acetophenone-d5 and triethoxyvinylsilane are limited.
Journal ArticleDOI
Catalytic C-H/olefin coupling
Shinji Murai,Fumitoshi Kakiuchi,S. Sekine,Yasuo Tanaka,Asayuki Kamatani,Motohiro Sonoda,Naoto Chatani +6 more
TL;DR: The cleavage and addition of ortho C-H bonds in various aromatic compounds such as ketones, esters, imines, imidates, nitrile, and aldehydes to olefins and acetlylenes can be achieved catalytically with the aid of ruthenium catalysts.
Journal ArticleDOI
Catalytic Addition of Olefinic C–H Bonds to Olefins
TL;DR: In this article, the addition of C-H bonds in α,β-enones to olefins was attained by Ru(H)2(CO)(PPh3)3 catalyst.
Journal ArticleDOI
Completely selective synthesis of (E)-β-(triethylsilyl) styrenes by Fe3(CO)12-catalyzed reaction of styrenes with triethylsilane
TL;DR: The reaction of styrene with treithylsilane, catalysed by OS3(CO)12, gave a mixture of the corresponding vinylsilane (dehydrogenative silylation product) and alkylsilane (hydrosilylation).