Yoichi Hoshimoto

Associate Professor

Japan

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About

Yoichi Hoshimoto is an Associate Professor at the Faculty of Engineering, Osaka University, Japan (country code: 81). His research areas include boron-based ligands, triarylborane chemistry, and sustainable catalytic processes. Recent articles highlight his work on the synthesis and reactivity of various chemical compounds, including carborane-substituted arenes and the modulation of electronic environments in metal centers.

Articles (18)

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2025

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2021

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2020

Collaborators (3)

Shinobu Takizawa

Osaka University

JAPAN

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Han Vinh Huynh

National University of Singapore (NUS)

SINGAPORE

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Yuta UETAKE

Assistant Professor

Osaka University

JAPAN

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Yoichi Hoshimoto

Research Interests

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About

Articles (18)

Monodentate σ-Accepting Boron-Based Ligands Bearing Square-Planar Ni(0) Centers

An Isolated Lithium ortho-Carboranyl Cuprate Complex for the Synthesis of Multiple-Carborane-Substituted Arenes from (Hetero)Aryl Bromides and Chlorides

Boosting Turnover in the Triarylborane-Catalyzed Hydrogenation of N-Substituted Indoles via Olefin-to-Nitrogen Lewis Base Switching in H2-Cleavage Steps

Transformation of CO2 and isocyanates mediated by N-borane-substituted cyclic phosphine imides (BCPIs) via λ5-oxazaphosphetanes

Electronic Profiling of <i>N</i>-Phosphine Oxide-Substituted Imidazolin-2-ylidenes (PoxIms) and Imidazolidin-2-ylidenes (SPoxIms)

Recent Trends in Triarylborane Chemistry: Diversification of Structures and Reactivity via meta-Substitution of the Aryl Groups

In-silico-assisted derivatization of triarylboranes for the catalytic reductive functionalization of aniline-derived amino acids and peptides with H2

Strategic use of crude H2 for the catalytic reduction of carbonyl compounds

Reversible Modulation of the Electronic and Spatial Environment around Ni(0) Centers Bearing Multifunctional Carbene Ligands with Triarylaluminum

Remote Back Strain: A Strategy for Modulating the Reactivity of Triarylboranes

Complexation-induced N‒P axial chirality in Sm(II) N-phosphine oxide-substituted imidazolylidene and imidazolinylidene complexes

Main group catalysis for H 2 purification based on liquid organic hydrogen carriers

Room-Temperature Reversible Chemisorption of Carbon Monoxide on Nickel(0) Complexes

A boron-transfer mechanism mediating the thermally induced revival of frustrated carbene–borane pairs from their shelf-stable adducts

Sm(II)-mediated Single-electron Reduction of Pentafluorophenylcopper(I)

N‐Phosphine Imide‐Substituted Imidazolylidenes

Development of Metal Complexes Equipped with Structurally Flexible Carbenes

Axial Chirality around N–P Bonds Induced by Complexation between E(C6F5)3 (E = B, Al) and an N-Phosphine Oxide-Substituted Imidazolinylidene: A Key Intermediate in the Catalytic Phosphinoylation of CO2

Collaborators (3)

Shinobu Takizawa

Han Vinh Huynh

Yuta UETAKE

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