記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： https://doi.org/10.1021/acscatal.1c03076

その他リンク： https://pubs.acs.org/doi/10.1021/acscatal.1c03076

記述言語：英語   掲載種別：研究論文（学術雑誌）  

その他リンク： https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/cctc.202101092

記述言語：英語   掲載種別：研究論文（学術雑誌）  

Bifunctional phosphonium/thioureas derived from tert-leucine behaved as highly selective catalysts for enantioselective protonation of enol esters, providing α-chiral ketones in yields of up to 99% with high enantioselectivities (up to 98.5:1.5 er). Control experiments clarified that a bulky tert-butyl group and phosphonium and thiourea moieties were necessary to achieve such high stereoselectivity. In addition, mechanistic investigations indicated the catalyst was converted to the corresponding betaine species, which served as a monomolecular catalyst.

DOI： 10.1021/acs.orglett.9b01216

その他リンク： https://pubs.acs.org/doi/10.1021/acs.orglett.9b01216

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1021/acscatal.8b00693

その他リンク： https://pubs.acs.org/doi/10.1021/acscatal.8b00693

記述言語：英語   掲載種別：研究論文（学術雑誌）  

Enantioselective 1,1-diarylation of terminal alkenes enabled by the combination of Pd catalysis with a chiral anion phase transfer (CAPT) strategy is reported herein. The reaction of substituted benzyl acrylates with aryldiazonium salts and arylboronic acids gave the corresponding 3,3-diarylpropanoates in moderate to good yields with high enantioselectivies (up to 98:2 er). Substituents on the benzyl acrylate and CAPT catalyst significantly affect the enantioselectivity, and multidimensional parametrization identified correlations suggesting structural origins for the high stereocontrol.

DOI： 10.1021/jacs.6b11367

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1002/chem.201604021

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

出版者・発行元：Applied Catalysis B Environmental  

The isomerization of allylic esters using zirconia-supported Au nanoparticle (NP) catalysts is an attractive solution for the efficient utilization and transformation of C4 derivatives in current industrial processes. The catalytic isomerization of allylic esters using zirconia-supported Au NPs was demonstrated to be both economical and environmentally friendly. This study introduces a novel application of gold catalysis for the transformation of but-3-ene-1,2-diyl diacetate (3,4-DABE) and but-2-ene-1,4-diyl diacetate (1,4-DABE), which are valuable intermediates for butanediol or tetrahydrofuran production. The reaction proceeded efficiently under solvent-free conditions, and the optimal catalysts exhibited high activity and stability. The Koros-Nowak criterion test and reaction condition modulation were conducted to optimize the catalytic efficiency. Catalysts with high gold loadings proved to be more efficient on a per-gold-atom basis. The partial pressure of oxygen was revealed to be a critical factor influencing the performance of supported Au NP catalysts in both batch and flow reactions. In particular, the oxygen atmosphere provided a modifying function to the surface of the supported Au NPs, facilitating the formation and maintenance of the Au^δ+ component, which is the active species with soft Lewis acidic properties. Theoretical calculations revealed that adsorption of oxygen molecules facilitated this reaction. Crucially, the catalytic system maintained its performance during a 50-day continuous-flow reaction scaled up to the kilogram level, confirming its suitability for industrial applications. This study highlights the economic and environmental benefits of the isomerization process and its potential as a practical solution for the industrial transformation of C4 derivatives.

DOI： 10.1016/j.apcatb.2025.125351

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出版者・発行元：Elsevier BV  

DOI： 10.2139/ssrn.5110250

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記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： https://doi.org/10.1002/tcr.202300148

その他リンク： https://onlinelibrary.wiley.com/doi/full/10.1002/tcr.202300148

記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Chemical Record  

Heterogeneous noble metal catalysts exhibit various functions. Although their redox functions have been extensively studied, we focused on their soft Lewis acid functions. Supported Au, Pt, and Pd catalysts electrophilically attack the π-electrons of soft bases such as alkynes, alkenes, and aromatic compounds to perform addition and substitution reactions. Hydroamination, intramolecular cyclization of alkynyl carboxylic acids, isomerization of allylic esters, vinyl exchange reactions, Wacker oxidation, and oxidative homocoupling of aromatics are introduced based on a discussion of the active species and reaction mechanisms. Furthermore, the adsorption of sulfur compounds, which are soft bases, onto the supported AuNPs is discussed. The adsorption and removal of 1,3-dimethyltrisulfane (DMTS), which is the compound responsible for the stale odor of “hine-ka” in alcoholic beverages, particularly Japanese sake, is described.

DOI： 10.1002/tcr.202300148

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担当区分：筆頭著者,　責任著者   記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ACS Catalysis  

Herein, we report a heterogeneous cobalt-catalyzed H2S-reagent-free synthetic method for 1,2-bis(2,4,4-trimethylpentan-2-yl)polysulfanes, which have been used as extreme-pressure additives in the field of tribology and have been produced worldwide in the tens of thousands of tonnes per year. The current industrial synthetic processes typically use hydrogen sulfide as the reductant, but improvements are needed in terms of the toxicity and the cost associated with safety control. The present reaction with Co3O4 and Na-X zeolite as catalysts provides the corresponding polysulfanes with three to eight sulfur atoms from diisobutylene, hydrogen, and elemental sulfur in up to 88% yield under neat reaction conditions. Experimental and density functional theory (DFT) mechanistic investigations provide insights into the roles of Na-X zeolite and cobalt catalysts. The DFT calculations suggest that heterolytic H2 activation with cobalt polysulfide species and subsequent protonation of alkenes and the C-S bond formation take place in a single step by a terminal SSH group in the cobalt polysulfide species, which provides a reasonable interpretation of the observed Markovnikov selectivity.

DOI： 10.1021/acscatal.3c03545

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記述言語：日本語   掲載種別：研究論文（学術雑誌）  

その他リンク： https://www.sciencedirect.com/science/article/pii/S2468823123005436

掲載種別：研究論文（学術雑誌）   出版者・発行元：Molecular Catalysis  

Gold nanoparticles supported on SiO2, Al2O3, TiO2, and carbon (Maxsorb, Ketjen black and Shirasagi New Gold) were prepared by impregnation and solid grinding methods using N-heterocyclic carbene (NHC)-Au complexes as precursors. A total of nine NHC-Au complex precursors were tested by impregnation and solid grinding method, and [Au(OH)(IPr)] (IPr = 1,3-bis(2,6-diisopropylphenyl)1,3-dihydro-2H-imidazol-2-ylidene) complex led to (1–2 nm) particle sizes by both methods. The prepared catalysts were characterized by XRD (X-ray diffraction), HAADF-STEM (high-angle annular dark-field scanning transmission electron microscopy), in situ XAFS (X-ray absorption fine structure), etc. In addition, [Au(OH)(IPr)] and its impregnated [Au(OH)(IPr)]/SiO2 were subjected to TG-DTA (thermogravimetry analysis-differential thermal analysis) and in situ XAFS analysis under calcination conditions, respectively. Moreover, the obtained supported Au nanoparticles (NPs) were effective as catalysts for low-temperature CO oxidation, intramolecular cyclization of alkynyl carboxylic acids, and isomerization of allylic esters. Their results suggested that the reduction of [Au(OH)(IPr)] proceeds rapidly from around 300°C, and the residual ligands should be attached to the surface of the Au NPs and protect them from drastic agglutination. These results reveal that properly designed NHC-Au complexes can facilitate the preparation of supported Au NP catalysts with small particle sizes and high activities.

DOI： 10.1016/j.mcat.2023.113460

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担当区分：筆頭著者,　責任著者   記述言語：日本語   掲載種別：研究論文（学術雑誌）  

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記述言語：日本語   出版者・発行元：公益社団法人 有機合成化学協会  

An ester group is one of ubiquitous and important functional groups in the field of organic chemistry. Stereoselective transformations of substrates having ester groups using artificial catalysts such as metal complexes and organocatalysts have been developed such as 1,4–addition of α,β –unsaturated esters and functionalizations at α –carbon of esters. However, stereoselective transformations of the ester group itself have been still highly limited. Hydrolase–catalyzed asymmetric hydrolysis of esters, which is a basic and important reaction categorized as the latter reaction type, has long been studied, and widely used from the lab scale to the industrial scale synthesis. However, enzymatic reactions generally have several issues such as their low specific activity and high cost. Under these circumstances, we hypothesized that stereoselective base hydrolysis of esters would be achieved by using liquid–liquid biphasic system with chiral onium salt catalysts. Herein, we describe the asymmetric base hydrolysis of esters using chiral onium salt catalysts derived from Cinchona alkaloids and chiral amino acids as well as the related dynamic kinetic resolution of azlactones via phase–transfer catalytic base alcoholysis. In addition, we also demonstrated the computational investigations using ConFinder program with pseudo–transition state conformational search (PTSCS) method.

DOI： 10.5059/yukigoseikyokaishi.81.798

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：RSC Advances  

A metal-organic framework (MOF) having a redox active 1,4,5,8-naphthalenetetracarboxdiimide (NDI) derivative in its organic linker shows excellent rate performance as an electrode material for aqueous batteries thanks to its large pores. Among aqueous electrolytes examined, K+-based ones exhibit the highest rate performance, which is caused by the highest mobility of the smallest hydrated K+ ion not only in the aqueous electrolyte but also in the electrode. Since the use of a counter electrode with insufficiently small pores for the full-cell configuration offsets this merit, our study may lead to a conclusion that the maximum rate performance for aqueous batteries will be accomplished only through further elaboration of both electrode materials with sufficiently large pores, in which hydrated ions can travel equally fast as those in the electrolyte.

DOI： 10.1039/d3ra03187j

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記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： DOI: 10.1039/d3ra03187j

その他リンク： https://pubs.rsc.org/en/content/articlelanding/2023/ra/d3ra03187j

掲載種別：研究論文（学術雑誌）   出版者・発行元：Bulletin of the Chemical Society of Japan  

To extend the lifetime and improve the safety of lithium-ion batteries, the decomposition mechanism of electrolytes in lithium-ion batteries was kinetically and stereospecifically studied in simplified reaction systems, which were in contact with the charged positive electrodes including Li1-x CoO2 as an active material removed from batteries. By identifying the products, mainly vinylene carbonate (VC) was detected by gas chromatography as an oxidation product of ethylene carbonate (EC). The kinetic isotope effects of the reaction were evaluated using EC and deuterium-labeled ECD4. The kH/kD was found to be 2.9 suggesting the C-H bond cleavage step was irreversible and corresponds to the rate-determining step of the overall process in the reaction. Also, Arrhenius and Eyring plots and stereospecific studies using syn-substituted EC-D2 indicated that the transition state has a rigid structure and that the elimination of hydrogens from EC proceeded mainly via syn stereochemistry. Upon a change in the charge potential of Li1-xCoO2 from 4.5V to 4.1V, the rate of formation of VC decreased.

DOI： 10.1246/bcsj.20230027

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記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： https://doi.org/10.1246/bcsj.20230027

その他リンク： https://academic.oup.com/bcsj/article-abstract/96/5/444/7332876?redirectedFrom=fulltext

掲載種別：研究論文（学術雑誌）   出版者・発行元：Catalysis Today  

Metal oxides supported platinum catalysts with residual chloride are known to be reusable soft Lewis acid catalysts for the isomerization of allylic esters. To deepen the understanding of the industrial application of the catalytic system and optimize the catalyst design, an investigation on the reusability and deactivation mechanism of supported platinum catalysts in the isomerization of but-3-ene-1,2-diyl diacetate was conducted. A great reactivation effect was observed by treating the used catalysts with HCl, rather than that of calcination. Pt-Cl/CeO2 showed the best reusability among the catalysts prepared with other metal oxides, and it was uncovered that the reduction of PtOxCly species should be the main reason for deactivation with the assistance of X-ray absorption fine structure (XAFS) analysis. Besides, a relatively stable state was also observed from the XAFS spectra of Pt-Cl/CeO2 catalysts in the reusing test, and it could effectively prevent the active species from further deactivation. Furthermore, in an extended evaluation of the stability of the catalysts, reusability, and a limited deactivation were also verified through a 10-run batch reaction. Additionally, the continuous flow reaction was also proven to be feasible.

DOI： 10.1016/j.cattod.2022.06.007

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担当区分：筆頭著者,　責任著者   記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of Organic Chemistry  

A detailed theoretical mechanistic investigation on the dynamic kinetic resolution of N-protected amino acid esters using phase-transfer catalysts is described. Semiautomatic exhaustive conformation search of transition state (TS)-like structures were carried out using the ConFinder program and the pseudo-TS conformational search (PTSCS) method. This conformational search method successfully provided reasonable TS structures for determining the stereoselectivity in the asymmetric base hydrolysis of hexafluoroisopropyl (HFIP) esters as well as the racemization mechanism. Furthermore, the independent gradient model (IGM) analysis of the TS structures suggested that the H-bonding interactions with the oxyanion hole and π-stacking interactions are the common important features of the proposed TS structures that determine the stereoselectivity.

DOI： 10.1021/acs.joc.2c02352

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記述言語：英語   出版者・発行元：Royal Society of Chemistry (RSC)  

A metal–organic framework (MOF) having a redox active 1,4,5,8-naphthalenetetracarboxdiimide (NDI) derivative in its organic linker shows excellent rate performance as an electrode material for aqueous batteries thanks to its large pores. Among aqueous electrolytes examined, K+-based ones exhibit the highest rate performance, which is caused by the highest mobility of the smallest hydrated K+ ion not only in the aqueous electrolyte but also in the electrode. Since the use of a counter electrode with insufficiently small pores for the full-cell configuration offsets this merit, our study may lead to a conclusion that the maximum rate performance for aqueous batteries will be accomplished only through further elaboration of both electrode materials with sufficiently large pores, in which hydrated ions can travel equally fast as those in the electrolyte.

CiNii Research

掲載種別：研究論文（学術雑誌）   出版者・発行元：Journal of Cleaner Production  

When producing liquid fuels from petroleum, hydrodesulfurization methods reduce the concentration of sulfur to ≤10 mg(S)/L (weight/volume concentration of sulfur), namely, ≤ 0.31 mmol/L. Dibenzothiophene derivatives (DBTs), which are known as particularly difficult desulfurizing substances, have been decomposed reductively in severe conditions of high temperatures (270–372 °C) and high pressure (50–102 atm of H2). In this study, we developed a UV light irradiation-based desulfurization method for aromatic sulfur compounds such as benzothiophene derivatives (BTs) and DBTs under room temperature and atmospheric pressure without the use of catalysts or additives. This method is simple, location-independent, and low-cost, and has low environmental impact. BTs and DBTs completely decomposed in approximately 8 h and 16 h, respectively, under ultraviolet (UV) light irradiation (λ = 254 nm) from a 8 W lamp. The yellow precipitates that were produced upon decomposition were confirmed to be sulfur allotropes (Sn). The residual hydrocarbon portion of DBT after sulfur removal was determined to be benzene. The decomposition reaction was determined to exhibit pseudo-first-order reaction. DFT calculations confirmed the degradation mechanism as follows: UV light irradiation induces a photochemically excited triplet state of DBTs. The excited DBTs reacts with O2 to form a π-complex, which isomerizes to a more stable σ-complex. The DBTs-O2 (σ-complex) then reacts with free DBTs to afford two molecules of dibenzothiophene-5-oxide derivatives (DBTOs), which are excited to singlet states on photoirradiation. The excited DBTOs isomerize through a minimum energy intersection eventually to dibenzofuran episulfides from which sulfur extrusion occurs.

DOI： 10.1016/j.jclepro.2022.133402

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担当区分：責任著者   掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis A: General  

β-Hydroxy β-methylbutyric acid (HMB) is expected as a promising therapeutic agent or a supplement. For industrial production of HMB, Pt-catalyzed aerobic oxidation of isoprene glycol is a potent synthetic method. However, the previous report using Pt-Bi catalyst supported on active carbon suffered from low tolerance to high substrate concentration conditions, which leads to low volumetric productivity. Herein, we report aerobic oxidation of isoprene glycol using Pt-Bi catalysts supported on ZrO2 or TiO2, showing high tolerance to the high substrate concentration conditions. In addition, these catalysts exhibited high recyclability. Scanning transmission electron microscopy analyses suggested the Pt-Bi species supported on ZrO2 or TiO2 are less likely to aggregate than those supported on activated carbon. Additionally, these metal oxides supported catalysts showed lower metal leaching than the carbon supported catalysts. Besides, the results of the various control experiments indicated the prevention of dehydration of an aldehyde intermediate is important for further improvement.

DOI： 10.1016/j.apcata.2022.118781

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担当区分：責任著者   記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Applied Catalysis A: General  

Zirconia-supported sodium-salt-modified Au(0) nanoparticles (NPs) (Na-Au/ZrO2) catalyst was prepared, and it was stable and recyclable in the intramolecular cyclization of alkynoic acids. In particular, the effect of sodium species in Na-Au/ZrO2, which has been overlooked in previous studies, was studied, and they were found to play an essential role in the reaction. In addition, the relationship between the kinetics and size of Au NPs revealed that the active sites of the catalyst are located on the surface of the supported Au NPs. Moreover, detailed kinetic studies revealed that the cyclization was a zero-order reaction with respect to substrate concentration, and the rate-determining step of the reaction is presumed to be protodeauration. The maximum turnover number (TON) of the reaction of 5-hexynoic acid in a continuous flow reactor exceeded 9000, which is the highest TON obtained in the presence of a heterogeneous Au catalyst.

DOI： 10.1016/j.apcata.2022.118765

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： https://doi.org/10.1016/j.jclepro.2022.133402

その他リンク： https://www.sciencedirect.com/science/article/pii/S0959652622029857?via%3Dihub

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： https://doi.org/10.1016/j.cattod.2022.06.007

その他リンク： https://www.sciencedirect.com/science/article/pii/S0920586122002292

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1055/a-1468-1455

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： doi.org/10.1016/j.mcat.2019.110502

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.mcat.2019.110502

その他リンク： https://www.sciencedirect.com/science/article/pii/S2468823119303402?via%3Dihub

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.apcatb.2019.01.031

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1055/s-0036-1590835

記述言語：英語   掲載種別：研究論文（学術雑誌）  

A mechanistic study of the Pd-catalyzed enantioselective 1,1-diarylation of benzyl acrylates that is facilitated by a chiral anion phase transfer (CAPT) process is presented. Kinetic analysis, labeling, competition, and nonlinear effect experiments confirm the hypothesized general mechanism and reveal the role of the phosphate counterion in the CAPT catalysis. The phosphate was found to be involved in the phase transfer step and in the stereoinduction process, as expected, but also in the unproductive reaction that provides the traditional Heck byproduct. Multivariate correlations revealed the CAPT catalyst’s structural features, affecting the production of this undesired byproduct, as well as weak interactions responsible for enantioselectivity. Such putative interactions include π-stacking and a CH···O electrostatic attraction between the substrate benzyl moiety and the phosphate. Analysis of the computed density functional theory transition structures for the stereodetermining step of the reaction supports the multivariate model obtained. The presented work provides the first comprehensive study of the combined use of CAPT and transition metal catalysis, setting the foundation for future applications.

DOI： 10.1021/jacs.7b06917

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1021/acs.organomet.7b00476

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1002/cssc.201701016

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

記述言語：英語   掲載種別：研究論文（学術雑誌）  

開催年月日： 2024年12月

会議種別：ポスター発表  

開催地：宮崎   国名：日本国  

開催年月日： 2024年4月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2024年4月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2023年9月

記述言語：日本語  

開催地：札幌   国名：日本国  

開催年月日： 2023年9月

記述言語：日本語  

開催地：札幌   国名：日本国  

開催年月日： 2023年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2023年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2023年6月

記述言語：その他   会議種別：口頭発表（一般）  

開催地：福岡   国名：日本国  

開催年月日： 2023年6月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：Fukuoka   国名：日本国  

開催年月日： 2023年5月

記述言語：日本語  

開催地：Seoul   国名：大韓民国  

開催年月日： 2023年5月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：Seoul   国名：大韓民国  

開催年月日： 2023年5月

記述言語：日本語  

開催地：Seoul   国名：大韓民国  

開催年月日： 2023年5月

記述言語：日本語  

開催地：Seoul   国名：日本国  

開催年月日： 2023年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2023年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2023年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2023年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2023年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2022年10月

記述言語：日本語  

開催地：東京   国名：日本国  

開催年月日： 2022年9月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2022年9月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：富山   国名：日本国  

開催年月日： 2022年9月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：富山   国名：日本国  

開催年月日： 2022年9月

記述言語：日本語  

開催地：茨城   国名：日本国  

開催年月日： 2022年8月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：佐賀   国名：日本国  

開催年月日： 2022年7月 - 2022年8月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2022年7月

記述言語：日本語  

開催地：Fukuoka   国名：日本国  

開催年月日： 2022年7月

記述言語：日本語  

開催地：福岡   国名：日本国  

開催年月日： 2022年7月

記述言語：日本語  

開催地：福岡   国名：日本国  

開催年月日： 2022年6月

記述言語：日本語  

開催地：福岡   国名：日本国  

開催年月日： 2022年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2022年3月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2022年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2022年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2022年1月

記述言語：日本語  

開催地：熊本   国名：日本国  

開催年月日： 2021年9月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2021年9月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2021年9月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2021年8月

記述言語：日本語  

開催地：WEB   国名：日本国  

開催年月日： 2021年7月

記述言語：日本語  

開催地：WEB   国名：日本国  

開催年月日： 2021年7月

記述言語：日本語  

開催地：WEB   国名：日本国  

開催年月日： 2021年7月

記述言語：日本語  

開催地：WEB   国名：日本国  

開催年月日： 2021年7月

記述言語：日本語  

開催地：WEB   国名：日本国  

開催年月日： 2021年3月

記述言語：日本語   会議種別：口頭発表（一般）  

国名：日本国  

開催年月日： 2020年10月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2020年10月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2020年10月

記述言語：日本語  

開催地：オンライン   国名：日本国  

開催年月日： 2020年10月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2020年10月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：オンライン   国名：日本国  

開催年月日： 2020年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2020年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2020年3月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：千葉   国名：日本国  

開催年月日： 2019年11月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：名古屋   国名：日本国  

開催年月日： 2019年9月

記述言語：日本語  

開催地：長崎   国名：日本国  

開催年月日： 2019年9月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：長崎   国名：日本国  

開催年月日： 2019年7月 - 2018年7月

記述言語：英語   会議種別：口頭発表（一般）  

開催地：Paris   国名：フランス共和国  

開催年月日： 2019年7月

記述言語：日本語   会議種別：口頭発表（一般）  

開催地：北九州   国名：日本国  

開催年月日： 2019年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2019年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2019年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2019年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2019年7月

記述言語：日本語  

開催地：北九州   国名：日本国  

開催年月日： 2019年6月

記述言語：英語  

開催地：Kumamoto   国名：日本国  

開催年月日： 2019年3月

記述言語：日本語  

開催地：Singapore   国名：シンガポール共和国  

開催年月日： 2018年7月

記述言語：英語   会議種別：口頭発表（一般）  

開催地：Krakow   国名：ポーランド共和国  

開催年月日： 2017年10月

記述言語：日本語  

開催地：Tokyo   国名：日本国  

開催年月日： 2016年11月

記述言語：英語   会議種別：口頭発表（一般）  

開催地：Taipei   国名：台湾  

開催年月日： 2016年9月

記述言語：日本語  

国名：日本国  

記述言語：英語  

DOI： 10.1055/s-0036-1588772

記述言語：日本語   掲載種別：記事・総説・解説・論説等（学術雑誌）  

記述言語：日本語   掲載種別：記事・総説・解説・論説等（学術雑誌）