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Aya Suzuki

Researcher at University of Tokyo

Publications -  67
Citations -  1213

Aya Suzuki is an academic researcher from University of Tokyo. The author has contributed to research in topics: Catalysis & Market power. The author has an hindex of 18, co-authored 59 publications receiving 1002 citations. Previous affiliations of Aya Suzuki include University of Tsukuba & National Graduate Institute for Policy Studies.

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Chiral Metal Nanoparticle Systems as Heterogeneous Catalysts beyond Homogeneous Metal Complex Catalysts for Asymmetric Addition of Arylboronic Acids to α,β-Unsaturated Carbonyl Compounds.

TL;DR: It is found that characteristic features of the nanoparticle system were totally different from those of the metal complex system, and showed performance in terms of yield, enantioselectivity, and catalytic turnover that was superior to that of the corresponding homogeneous metal complexes.
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Local and Personal Networks in Employment and the Development of Labor Markets: Evidence from the Cut Flower Industry in Ethiopia

TL;DR: In this article, the roles of local and personal networks in the employment process and the emergence and development of the labor market in Ethiopia's growing cut flower industry were examined and found that workers who were recruited informally using the social ties were paid less than the formally-recruited workers at hiring.
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Polysilane-Immobilized Rh-Pt Bimetallic Nanoparticles as Powerful Arene Hydrogenation Catalysts: Synthesis, Reactions under Batch and Flow Conditions and Reaction Mechanism.

TL;DR: Details of the reaction mechanisms and the origin of different kinetics in batch and flow were studied, and the obtained knowledge was applied to develop completely selective arene hydrogenation of compounds containing two aromatic rings toward the synthesis of an active pharmaceutical ingredient.
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Distribution of myofiber types in thigh muscles of chickens

TL;DR: The spatial distribution of myofiber types within individual muscles can account for the various locomotory and postural requirements of the thigh.
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Feasibility of ex vivo gene therapy for neurological disorders using the new retroviral vector GCDNsap packaged in the vesicular stomatitis virus G protein.

TL;DR: A new retrovirus production system in which the simplified retroviral vector GCDNsap engineered to be resistant to denovo methylation was packaged in the vesicular stomatitis virus G protein, concentrated by centrifugation, and resuspended in serum‐free medium (StemPro‐34 SFM).