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Masahiro Murakami

Researcher at Kyoto University

Publications -  694
Citations -  20243

Masahiro Murakami is an academic researcher from Kyoto University. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 72, co-authored 672 publications receiving 18238 citations. Previous affiliations of Masahiro Murakami include University of Tokyo & Gifu University.

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Rhodium-catalyzed annulation reactions of 2-cyanophenylboronic acid with alkynes and strained alkenes.

TL;DR: A new [3 + 2] annulation reaction was developed in which 2-cyanophenylboronic acid reacted as a three-carbon component with alkynes or alkenes to afford substituted indenones or indanones.
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Downward transport of organic carbon by diel migratory micronekton in the western equatorial Pacific:: its quantitative and qualitative importance

TL;DR: Using simultaneous sampling with a commercial-sized trawl, a zooplankton net, and a sediment trap, this paper evaluated the contribution of vertically migrating micronekton to vertical material transport (biological pump) at two stations (3°00′N, 146°00)E and 3°30′ N, 145°20′E) in the western equatorial North Pacific.
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Regiocontrolled Synthesis of Polysubstituted Pyrroles Starting from Terminal Alkynes, Sulfonyl Azides, and Allenes

TL;DR: 1-Sulfonyl-1,2,3-triazoles, readily prepared from terminal alkynes and sulfonyl azides, react with allenes in the presence of a nickel(0) catalyst to produce the corresponding isopyrroles.
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Enantioselective Insertion of a Carbenoid Carbon into a C–C Bond To Expand Cyclobutanols to Cyclopentanols

TL;DR: When a carbenoid species generated from a tosylhydrazone is reacted with a cyclobutanol in the presence of a chiral rhodium catalyst, a C-C single bond of the cyclobUTanol is cleaved, and the carbenoids carbon is inserted therein to furnish a ring-expanded cyclopentanol in an enantioselective manner.
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Ruthenium-Mediated Regio- and Stereoselective Alkenylation of Pyridine

TL;DR: Treatment of (alkyn-1-yl)trimethylsilane with pyridine in the presence of a cationic ruthenium complex [CpRu(PPh(3))(2)]PF(6) affords the corresponding (E)-2-alkenylpyridineIn good yield in a regio- and stereoselective manner.