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Tamio Hayashi. Dichloro [1, 1'-bis (diphenylphosphino) ferrocene] palladium (II): an effective catalyst for cross-coupling of secondary and primary alkyl Grignard and alkylzinc reagents with …....
Tamio Hayashi is a professor at Kyoto University, Japan, who studies asymmetric organic reactions catalyzed by transition metal complexes. His publications include topics such as iridium-catalyzed allylic substitution, rhodium-catalyzed arylation of enynes, and chiral diene ligands.
Tamio Hayashi's 561 research works with 42,756 citations and 5,085 reads, including: Rhodium-Catalyzed Asymmetric Conjugate Addition to γ-Substituted α,β-Unsaturated γ-Lactams through Dynamic...
Jul 31, 2015 · A team led by Prof Tamio HAYASHI from the Department of Chemistry in NUS and Institute of Materials Research and Engineering (IMRE), has found a new synthetic route to chiral triarylmethanes, using an asymmetric substitution reaction of diarylmethylamines with arylboron reagents in the presence of a rhodium catalyst coordinated with ...
Tamio Hayashi is a Japanese chemist who specializes in synthetic organic chemistry, organometallic chemistry and catalysis. He is a professor at the National University of Singapore and has published many papers on asymmetric catalysis and new carbon–carbon bond forming reactions.
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Nickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes. Fei Xue ; Zhao Jin ; Hor Tzi Sum Andy ; Tamio Hayashi. 2. 2015. Rhodium-catalyzed asymmetric arylation of allyl sulfones under the conditions of isomerization into alkenyl sulfones.