{"id":348,"date":"2023-04-11T18:05:24","date_gmt":"2023-04-11T09:05:24","guid":{"rendered":"https:\/\/www2.fris.tohoku.ac.jp\/~tahara\/wordpress\/?page_id=348"},"modified":"2024-02-16T09:04:52","modified_gmt":"2024-02-16T00:04:52","slug":"papers","status":"publish","type":"page","link":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/research-result\/papers\/","title":{"rendered":"\u5b66\u8853\u8ad6\u6587\/\u7dcf\u8aac\u30fb\u8457\u66f8"},"content":{"rendered":"\n

\u3010Papers\u3011<\/h3>\n\n\n\n
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\u201cArylation of Hydrocarbyl Ligands Formed from n<\/em>-Alkanes through C-H Bond Activation of Benzene Using a Triruthenium Cluster\u201d<\/h4>\n\n\n\n

Makoto Moriya, Atsushi Tahara<\/u><\/strong>, Toshiro Takao, Hiroharu Suzuki<\/u><\/strong><\/p>\n\n\n\n

Eur. J. Inorg. Chem. <\/em>2009<\/strong>, 23<\/em>, 3393-3397.<\/a><\/p>\n\n\n\n

DOI: 10.1002\/ejic.200900519<\/p>\n\n\n

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\"Arylation<\/figure>\n<\/div>\n\n\n
\n<\/div><\/div>\n\n\n\n
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\u201cMetathesis Reaction of Hydrocarbyl Ligands across the Triruthenium Plane\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Mana Kajigaya, Makoto Moriya, Toshiro Takao, Hiroharu Suzuki<\/p>\n\n\n\n

Angew. Chem. Int. Ed. <\/em>2010<\/strong>, 49<\/em>(34), 5898-5901.<\/a><\/p>\n\n\n\n

DOI: 10.1002\/anie.201002235<\/p>\n\n\n\n

\u25cf Featured as Highlight (<\/u><\/strong>Angew. Chem. Int. Ed.<\/em> 2012, 51<\/em>, 5794-5796.<\/strong><\/a>)<\/u><\/strong><\/p>\n\n\n

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\"Metathesis<\/figure>\n<\/div>\n\n\n
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\u201cDevelopment of Metathesis Reaction of Hydrocarbyl Ligands using a Trimetallic Complex\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong><\/u><\/strong><\/p>\n\n\n\n

Bull. Jpn. Soc. Coord. Chem. <\/em>2011<\/strong>, 57<\/em>, 125-127<\/a>.<\/p>\n\n\n\n

DOI: 10.4019\/bjscc.57.125<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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\u201cSynthesis and dynamic properties of a triruthenium complex containing \u03bc<\/em>3<\/sub>–\u03b7<\/em>2<\/sup>(\u2225)-ethyne and \u03bc<\/em>3<\/sub>-methylidyne ligands: equilibrium of an ethyne-hydrido complex with a nonclassical \u03bc<\/em>3<\/sub>-vinyl complex\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Mana Kajigaya, Toshiro Takao, Hiroharu Suzuki<\/p>\n\n\n\n

Organometallics<\/em> 2013<\/strong>, 32<\/em>(1), 260-271<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/om301064y<\/p>\n\n\n

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\"Synthesis<\/figure>\n<\/div>\n\n\n
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\u201cMe2<\/sub>S-induced highly selective reduction of aldehydes in the presence of ketones involving aldehyde-selective rate enhancement: a triruthenium cluster-catalyzed hydrosilylations\u201d<\/h4>\n\n\n\n

Shohei Yumino, Toru Hashimoto, Atsushi Tahara<\/u><\/strong>, Hideo Nagashima<\/p>\n\n\n\n

Chem. Lett.<\/em> 2014<\/strong>, 43<\/em>(12), 1829-1831<\/a>.<\/p>\n\n\n\n

DOI: 10.1246\/cl.140731<\/p>\n\n\n

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\"Me2S-induced<\/figure>\n<\/div>\n\n\n
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\u201cRegio- and stereoselective synthesis of multisubstituted enamides by treatment of ynamides with boronic acids\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong><\/p>\n\n\n\n

J. Synth. Org Chem. Jpn. <\/em>2015<\/strong>, 73<\/em>(7), 749-750<\/a>.<\/p>\n\n\n\n

DOI: 10.5059\/yukigoseikyokaishi.73.749<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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\u201cCatalyst Design of Vaska-Type Iridium Complexes for Highly Efficient Synthesis of \u03c0<\/em>-Conjugated Enamines\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Yasumitsu Miyamoto, Ryuta Aoto, Keisuke Shigeta, Yuta Une, Yusuke Sunada, Yukihiro Motoyama, Hideo Nagashima<\/p>\n\n\n\n

Organometallics<\/em> 2015<\/strong>, 34<\/em>(20), 4895-4907<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.organomet.5b00636<\/p>\n\n\n

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\"Catalyst<\/figure>\n<\/div>\n\n\n
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\u201cNon-Precious-Metal Catalytic Systems Involving Iron or Cobalt Carboxylates and Alkyl Isocyanides for Hydrosilylation of Alkenes with Hydrosiloxanes\u201d<\/h4>\n\n\n\n

Daisuke Noda, Atsushi Tahara<\/u><\/strong>, Yusuke Sunada, Hideo Nagashima<\/p>\n\n\n\n

J. Am. Chem. Soc. <\/em>2016<\/strong>, 138<\/em>(8), 2480-2483<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/jacs.5b11311<\/p>\n\n\n\n

\u25cf Selected as Front Cover.<\/u><\/strong><\/p>\n\n\n\n

\u25cf Featured as Spotlight (<\/u><\/strong>J. Am. Chem. Soc.<\/em> 2016, 138<\/em>(8), 2455-2456.<\/strong><\/a>)<\/u><\/strong><\/p>\n\n\n\n

\u25cf Selected as \u201cSelect Research Articles from 2016\u201d in JACS<\/em><\/u><\/strong><\/p>\n\n\n\n

\u25cf Featured in <\/u><\/strong>Chem-Station (2016\/3\/9)<\/strong><\/a><\/p>\n\n\n\n

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\"Selected<\/figure>\n<\/div><\/div>\n\n\n\n
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\"Non-Precious-Metal<\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n
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\u201cTheoretical Study of the Catalytic Hydrogenation of Alkenes by a Disilaferracyclic Complex: Can the Fe-Si \u03c3<\/em>-Bond-Assisted Activation of H-H Bonds Allow Development of a Catalysis of Iron?\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Hiromasa Tanaka, Yusuke Sunada, Yoshihito Shiota, Kazunari Yoshizawa, Hideo Nagashima<\/p>\n\n\n\n

J. Org. Chem. <\/em>2016<\/strong>, 81<\/em>(22), 10900-10911<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.joc.6b01961<\/p>\n\n\n

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\"Theoretical<\/figure>\n<\/div>\n\n\n
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 \u201c\u03c3<\/em>-CAM mechanisms for the hydrogenation of alkenes by cis<\/em>– and trans<\/em>-disilametallacyclic carbonyl complexes (M = Fe, Ru, Os): experimental and theoretical studies\u201d<\/h4>\n\n\n\n

Konoka Hoshi, Atsushi Tahara<\/u><\/strong>, Yusuke Sunada, Hironori Tsutsumi, Ryoko Inoue, Hiromasa Tanaka, Yoshihito Shiota, Kazunari Yoshizawa, Hideo Nagashima<\/p>\n\n\n\n

Bull. Chem. Soc. Jpn. <\/em>2017<\/strong>, 90<\/em>(5), 613-626<\/a>.<\/p>\n\n\n\n

DOI: 10.1246\/bcsj.20170004<\/p>\n\n\n\n

\u25cf<\/u><\/strong> Selected as BCSJ award (Vol 90, No. 5, 2017)<\/u><\/strong><\/p>\n\n\n\n

\u25cf Selected as Front Cover<\/u><\/strong><\/p>\n\n\n\n

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\"Selected<\/figure>\n<\/div><\/div>\n\n\n\n
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\"s-CAM<\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n
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\u201cDisilaruthena- and Ferracyclic Complexes Containing Isocyanide Ligands as Effective Catalysts for Hydrogenation of Unfunctionalized Sterically Hindered Alkenes\u201d<\/h4>\n\n\n\n

Yusuke Sunada, Hajime Ogushi, Taiji Yamamoto, Shoko Uto, Mina Sawano, Atsushi Tahara<\/u><\/strong>, Hiromasa Tanaka, Yoshihito Shiota, Kazunari Yoshizawa, Hideo Nagashima<\/p>\n\n\n\n

J. Am. Chem. Soc. <\/em>2018<\/strong>, 140<\/em>(11), 4119-4134<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/jacs.8b00812<\/p>\n\n\n\n

\u25cf Selected as a Finalist of Supplementary Front Cover<\/u><\/strong><\/p>\n\n\n\n

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\"Selected<\/figure>\n<\/div>\n\n\n\n
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\"Disilaruthena-<\/figure>\n<\/div>\n<\/div>\n\n\n\n
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\u201cNovel application of nanoscale zero valent iron and bimetallic nano-Fe\/Cu particles for the treatment of cesium contaminated water\u201d<\/h4>\n\n\n\n

Tamer Shubair, Osama Eljamal, Ahmed M. E. Khali, Atsushi Tahara<\/u><\/strong>, Nobuhiro Matsunaga<\/p>\n\n\n\n

J. Environment. Chem. Eng.<\/em> 2018<\/strong>, 6<\/em>(4), 4253-4264<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.jece.2018.06.015<\/p>\n\n\n

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\"Novel<\/figure>\n<\/div>\n\n\n
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\u201cSyntheses of Substituted 1,4-Disila-2,5-cyclohexadienes from Cyclic Hexasilane Si6<\/sub>Me12<\/sub> and Alkynes via Successive Si-Si Bond Activation by Pd\/Isocyanide Catalysts\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Shunsuke Nagino, Yusuke Sunada, Ryohei Haige, Hideo Nagashima<\/p>\n\n\n\n

Organometallics<\/em> 2018<\/strong>, 37<\/em>(15), 2531-2453<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.organomet.8b00302<\/p>\n\n\n

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\"Syntheses<\/figure>\n<\/div>\n\n\n
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\u201cRemarkably high catalyst efficiency of a disilaruthenacyclic complex for hydrosilane reduction of carbonyl compounds\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Yusuke Sunada, Takashi Takeshita, Ryoko Inoue, Hideo Nagashima<\/p>\n\n\n\n

Chem. Commun. <\/em>2018<\/strong>, 54<\/em>(79), 11192-11195<\/a>.<\/p>\n\n\n\n

DOI: 10.1039\/C8CC04780D<\/p>\n\n\n

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\"Remarkably<\/figure>\n<\/div>\n\n\n
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\u201cTransformation of a \u03bc<\/em>3<\/sub>-Benzyne Ligand into Phenol on a Cationic Triruthenium Cluster Supported by a \u03bc<\/em>3<\/sub>-Sulfido Ligand\u201d<\/h4>\n\n\n\n

Hiroki Chikamori, Atsushi Tahara<\/u><\/strong>, Toshiro Takao<\/p>\n\n\n\n

Organometallics<\/em> <\/a>2019<\/strong>, 38<\/em>(4), 527-535<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.organomet.8b00832<\/p>\n\n\n

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\"Transformation<\/figure>\n<\/div>\n\n\n
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\u201cIron based nanoparticles-zeolite composites for the removal of cesium from aqueous solutions\u201d<\/h4>\n\n\n\n

Osama Eljamal, Tamer Shubair, Atsushi Tahara<\/u><\/strong>, Yuji Sugihara, Nobuhiro Matsunaga<\/p>\n\n\n\n

J. Mol. Liq.<\/em> 2019<\/strong>, 277<\/em>, 613-623<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.molliq.2018.12.115<\/p>\n\n\n

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\"Iron<\/figure>\n<\/div>\n\n\n
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\u201cIridium-PPh3<\/sub> Catalysts for Conversion of Amides to Enamines\u201d<\/h4>\n\n\n\n

Yuta Une, Atsushi Tahara<\/u><\/strong>, Yasumitsu Miyamoto, Yusuke Sunada, Hideo Nagashima<\/p>\n\n\n\n

Organometallics<\/em> 2019<\/strong>, 38<\/em>(4), 852-862<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.organomet.8b00835<\/p>\n\n\n\n

\u25cf Selected as Supplementary Front Cover<\/u><\/strong><\/p>\n\n\n\n

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\"\u25cf<\/figure>\n<\/div><\/div>\n\n\n\n
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\"Iridium-PPh3<\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n
\n<\/div><\/div>\n\n\n\n
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\u201cMAO-free and extremely active catalytic system for ethylene tetramerization\u201d<\/h4>\n\n\n\n

Tae Hee Kim, Hyun Mo Lee, Hee Soo Park, Sung Dong Kim, Su Jin Kwon, Atsushi Tahara<\/u><\/strong>, Hideo Nagashima, Bun Yeoul Lee<\/p>\n\n\n\n

App. Organomet. Chem.<\/em> 2019<\/strong>, 33<\/em>(4), e4829<\/a>.<\/p>\n\n\n\n

DOI: 10.1002\/aoc.4829<\/p>\n\n\n\n

\u25cf<\/u><\/strong> Selected as Inside Front Cover<\/u><\/strong><\/p>\n\n\n\n

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\"\u25cf<\/figure>\n<\/div><\/div>\n\n\n\n
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\"MAO-free<\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n
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 \u201cPreparation of new magnetic zeolite nanocomposites for removal of strontium from polluted waters\u201d<\/h4>\n\n\n\n

Tamer Shubair, Osama Eljamal, Atsushi Tahara<\/u><\/strong>, Yuji Sugihara, Nobuhiro Matsunaga<\/p>\n\n\n\n

J. Mol. Liq.<\/em> 2019<\/strong>, 288<\/em>, 111026<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.molliq.2019.111026<\/p>\n\n\n

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\"Preparation<\/figure>\n<\/div>\n\n\n
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\u201cDonor-Acceptor \u03c0<\/em>-Conjugated Enamines: Functional Group Compatible Synthesis from Amides and Their Photoabsorption and Photoluminescence Properties\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Ikumi Kitahara, Daichi Sakata, Yoichiro Kuninobu, Hideo Nagashima<\/p>\n\n\n\n

J. Org. Chem. <\/em>2019<\/strong>, 84<\/em>(23), 15236-15254<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acs.joc.9b02267<\/p>\n\n\n\n

\u25cf Selected as a Finalist of Supplementary Front Cover<\/u><\/strong><\/p>\n\n\n\n

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\"\u25cf<\/figure>\n<\/div><\/div>\n\n\n\n
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\"Donor-Acceptor<\/figure>\n<\/div><\/div>\n<\/div>\n\n\n\n
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\u201cRecent topics of iridium-catalyzed hydrosilylation of tertiary amides to silylhemiaminals\u201d<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Hideo Nagashima<\/p>\n\n\n\n

Tetrahedron Lett. <\/em>2020<\/strong>, 61<\/em>(4), 151423 (8 pages)<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.tetlet.2019.151423<\/p>\n\n\n

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\"Recent<\/figure>\n<\/div>\n\n\n
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\u201cMagnetic Zeolite Synthesis for Efficient Removal of Cesium in a Lab-scale Continuous Treatment System.\u201d<\/h4>\n\n\n\n

Omar Falyouna, Osama Eljamal, Ibrahim Maamoun, Atsushi Tahara<\/u><\/strong>, Yuji Sugihara<\/p>\n\n\n\n

J. Col. Int. Eci<\/em>. 2020<\/strong>, 571<\/em>(1), 66-79<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.jcis.2020.03.028<\/p>\n\n\n

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\"Magnetic<\/figure>\n<\/div>\n\n\n
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\u201cIntramolecular Nitrene Transfer via the C\u2261N Bond Cleavage of Acetonitrile to a \u03bc<\/em>3<\/sub>-Alkylidyne Ligand on a Cationic Triruthenium Plane\u201d<\/h4>\n\n\n\n

Yusuke Takahashi, Atsushi Tahara<\/u><\/strong>, Toshiro Takao<\/p>\n\n\n\n

Organometallics <\/em>2020<\/strong>, 39,<\/em> 2888-2899.<\/a><\/p>\n\n\n\n

DOI: 10.1021\/acs.organomet.0c00393<\/p>\n\n\n

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\"Intramolecular<\/figure>\n<\/div>\n\n\n
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\u201cSustainable Iron-Making Using Oxalic Acid: The Concept, A Brief Review of Key Reactions, and An Experimental Demonstration of the Iron-Making Process\u201d<\/h4>\n\n\n\n

Phatchada Santawaja, Shinji Kudo, Aska Mori, Atsushi Tahara<\/u><\/strong>, Shusaku Asano, Jun-ichiro Hayashi<\/p>\n\n\n\n

ACS Sus. Chem. Eng. <\/em>2020<\/strong>, 8, 13292-13301<\/a>.<\/p>\n\n\n\n

DOI: 10.1021\/acssuschemeng.0c0359<\/p>\n\n\n

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\"Sustainable<\/figure>\n<\/div>\n\n\n
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\u201cThe Asymmetric Kharasch Addition \u201cOn Water\u201d Catalyzed by \u201cRhCl[(\u2013)-DIOP]\u201d Species\u201d,<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Hikaru Takao, Hiroshi Furuno, Hideo Nagashima<\/p>\n\n\n\n

Evergreen<\/em> 2021<\/strong>, 8<\/em>(3), 535-543<\/a>.<\/p>\n\n\n\n

DOI: 10.5109\/4491639<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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 \u201cAn effect of metal cations for the formation of oxalates from formates\u201d,<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong><\/p>\n\n\n\n

Res Ind. Sci. Res. Prom. Found.<\/em> 2021<\/strong>, 1-8.<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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\u201cChemical deposition of iron nanoparticles (Fe0) on titanium nanowires for efficient adsorption of ciprofloxacin from water\u201d,<\/h4>\n\n\n\n

Omar Falyouna, Ibrahim Maamoun, Khaoula Bensaida, Atsushi Tahara<\/u><\/strong>, Yuji Sugihara, Osama Eljamal<\/p>\n\n\n\n

Wat. Prac. Tech.<\/em> 2022<\/strong>, 17<\/em>(1), 75-83<\/a>.<\/p>\n\n\n\n

DOI: 10.2166\/wpt.2021.091<\/p>\n\n\n\n

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\u201cEncapsulation of iron nanoparticles with magnesium hydroxide shell for remarkable removal of ciprofloxacin from contaminated water\u201d,<\/h4>\n\n\n\n

Omar Falyouna, Ibrahim Maamoun, Khaoula Bensaida, Atsushi Tahara<\/u><\/strong>, Yuji Sugihara, Osama Eljamal,<\/p>\n\n\n\n

J. Col. Int. Sci.<\/em> 2022<\/strong>, 605<\/em>, 813-827<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.jcis.2021.07.154<\/p>\n\n\n

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\"Encapsulation<\/figure>\n<\/div>\n\n\n
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\u201cSynthesis of hybrid magnesium hydroxide\/magnesium oxide nanorods [Mg(OH)2<\/sub>\/MgO] for prompt and efficient adsorption of ciprofloxacin from aqueous solutions\u201d,<\/h4>\n\n\n\n

Omar Falyouna, Khaoula Bensaida, Ibrahim Maamoun, U. P. M. Ashik, Atsushi Tahara<\/u><\/strong>, Kazuya Tanaka, Noboru Aoyagi, Yuji Sugihara, Osama Eljamal,<\/p>\n\n\n\n

J. Clean. Prod.<\/em> 2022<\/strong>, 342<\/em>(15), 130949 (15 pages)<\/a>.<\/p>\n\n\n\n

DOI: 10.1016\/j.jclepro.2022.130949<\/p>\n\n\n

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\"Synthesis<\/figure>\n<\/div>\n\n\n
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\u201cHomogeneous catalyst modifier for alkyne semi-hydrogenation: systematic screening in an automated flow reactor and computational study on mechanisms\u201d,<\/h4>\n\n\n\n

Shusaku Asano, Samuel J. Adams, Yuta Tsuji, Kazunari Yoshizawa, Atsushi Tahara<\/u><\/strong>, Jun-ichiro Hayashi,<\/p>\n\n\n\n

React. Chem. Eng. <\/em>2022<\/strong>, 7<\/em>, 1818-1826<\/a>.<\/p>\n\n\n\n

DOI: 10.1039\/d2re00147k<\/p>\n\n\n\n

\u25cf Featured in <\/u><\/strong>Chem-Station (2022\/6\/6)<\/strong><\/a><\/p>\n\n\n

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\"Homogeneous<\/figure>\n<\/div>\n\n\n
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 \u201cOptimizing the magnetic separation of strontium ion using modified zeolite with nano iron particles\u201d<\/h4>\n\n\n\n

Tamer Shubair, Atsushi Tahara<\/u><\/strong>, Shahjalal Khandaker<\/p>\n\n\n\n

<\/em><\/a>Case Stud. Chem. Environ. Eng. <\/em>2022,<\/strong> 6, <\/em>100243 (10 pages)<\/a>.<\/em><\/p>\n\n\n\n

DOI: 10.1016\/j.cscee.2022.100243<\/p>\n\n\n

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\"Optimizing<\/figure>\n<\/div>\n\n\n
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\u201cDissolution of Iron Oxides Highly Loaded in Oxalic Acid Aqueous Solution for a Potential Application in Iron-Making\u201d,<\/h4>\n\n\n\n

Phatchada Santawaja, Shinji Kudo, Atsushi Tahara<\/u><\/strong>, Shusaku Asano, Jun-ichiro Hayashi,<\/p>\n\n\n\n

<\/em><\/a>ISIJ International<\/em> 2022<\/strong>, 62<\/em>(12), 2466-2475<\/a>.<\/em><\/em><\/p>\n\n\n\n

DOI: 10.2355\/isijinternational.isijint-2020-726<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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\u201cSynthesis of Oxalate from CO2<\/sub> and Cesium Carbonate Supported Over Porous Carbon\u201d,<\/h4>\n\n\n\n

Takuya Kiyozumi, Shinji Kudo, Aska Mori, Riku Mizoguchi, Atsushi Tahara<\/strong>, Shusaku Asano, Jun-ichiro Hayashi,<\/p>\n\n\n\n

<\/em><\/a>ISIJ International<\/em> 2022<\/strong>, 61(12), 2476-2482<\/a>.<\/em><\/em><\/em><\/p>\n\n\n\n

DOI: 10.2355\/isijinternational.isijint-2022-159<\/p>\n\n\n\n

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\u00a0*preprinted<\/mark> \u201cBase-Catalyzed Dehydrogenative Coupling of Formate Anions to Oxalates: Effect of Alkali Metal Cations\u201d,<\/h4>\n\n\n\n

Atsushi Tahara<\/u><\/strong>, Aska Mori, Jun-ichiro Hayashi, Shinji Kudo,<\/p>\n\n\n\n

<\/a>ChemRxiv<\/em> 2022<\/strong>, DOI: 10.26434\/chemrxiv-2022-6r93n<\/em><\/a>.<\/em><\/em><\/em><\/em><\/p>\n\n\n

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\"Base-Catalyzed<\/figure>\n<\/div>\n\n\n
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\u3010Reviews \/ essays\u3011  *written in Japanese.<\/h3>\n\n\n\n
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*<\/mark> \u201c\u30a2\u30eb\u30b1\u30f3\u306e\u30d2\u30c9\u30ed\u30b7\u30ea\u30eb\u5316\u7528\u9244\u30fb\u30b3\u30d0\u30eb\u30c8\u89e6\u5a92\u306e\u958b\u767a\u201d<\/h4>\n\n\n\n

\u6c38\u5cf6 \u82f1\u592b, \u771f\u5ddd \u6566\u55e3, \u7530\u539f \u6df3\u58eb<\/u><\/strong>, \u7802\u7530 \u7950\u8f14, \u4f5c\u7530 \u6643\u53f8, \u91ce\u7530 \u5927\u8f14,<\/p>\n\n\n\n

\u30b1\u30a4\u7d20\u5316\u5b66\u5354\u4f1a\u8a8c \u30c8\u30d4\u30c3\u30af\u30b9\u2015\u6628\u65e5\u4eca\u65e5\u305d\u3057\u3066\u660e\u65e5\u306e\u30b1\u30a4\u7d20\u5316\u5b66, 2016<\/strong>, 33<\/em>, 4-13.<\/p>\n\n\n\n

(*comment: This is a review about recent topics of iron- or cobalt-catalyzed hydrosilylation of alkenes with hydrosiloxane, which was published in Japanese silicone chemistry paper.)<\/p>\n\n\n\n

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*<\/mark> \u201c\u30d9\u30fc\u30b9\u30e1\u30bf\u30eb\u3068\u5178\u578b\u5143\u7d20\u306b\u3088\u308b\u5206\u5b50\u6d3b\u6027\u5316\u306e\u6700\u8fd1\u306e\u52d5\u5411\u201d<\/h4>\n\n\n\n

\u7530\u539f \u6df3\u58eb<\/u><\/strong><\/p>\n\n\n\n

Organometallic News <\/em>2017<\/strong>, 2<\/em>, 80.<\/p>\n\n\n\n

(*comment: This is a review about recent topics of bond activation using a cooperative interaction between base metal and main metal.)<\/p>\n\n\n\n

\n<\/div><\/div>\n\n\n\n
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*<\/mark> \u201c\u304a\u3089\u304c\u6625 \u5bc5\u5e74\u751f\u308c\u304a\u304a\u3044\u306b\u8a9e\u308b \u662d\u548c\u516d\u5341\u4e00\u5e74\u751f\u201d,<\/h4>\n\n\n\n

\u7530\u539f\u6df3\u58eb<\/u><\/strong>,<\/strong><\/p>\n\n\n\n

\u8fd1\u757f\u5316\u5b66\u5de5\u696d\u754c (\u304d\u3093\u304b), 2021<\/strong>, 74<\/em>(1), 24.<\/p>\n\n\n\n

(ISSN 0912-196X).<\/p>\n\n\n\n

(*comment: This is a new-year message of chemists born in 1986, which was published in Japanese organometallic chemistry paper.)<\/p>\n\n\n\n

\n<\/div><\/div>\n<\/div><\/div>\n","protected":false},"excerpt":{"rendered":"

\u3010Papers\u3011 \u201cArylation of Hydrocarbyl Ligands Formed from n-Alkanes through C-H Bond Activation of Benzene Using […]<\/p>\n","protected":false},"author":1,"featured_media":277,"parent":23,"menu_order":10,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-348","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/pages\/348","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/comments?post=348"}],"version-history":[{"count":84,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/pages\/348\/revisions"}],"predecessor-version":[{"id":1000,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/pages\/348\/revisions\/1000"}],"up":[{"embeddable":true,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/pages\/23"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/media\/277"}],"wp:attachment":[{"href":"https:\/\/www.pharm.tohoku.ac.jp\/~kankyo\/index.php\/wp-json\/wp\/v2\/media?parent=348"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}