Original Papers
(51) TBA, Transformation using dearomatization
Wu, Q.; Muto, K.*; Yamaguchi, J.*
Submitted
(50) Facile Generation of ortho-Quinodimethanes Toward Polycyclic Compounds
Inagaki, K.; Onozawa, Y.; Fukuhara, Y.; Yokogawa, D.; Muto, K.*; Yamaguchi, J.*
Submitted
(See also: ChemRxiv 2024, DOI: 10.26434/chemrxiv-2024-dnf75)
(49) 2H-Thiazolo[4,5-d][1,2,3]triazole: Synthesis, Functionalization, and Application in Scaffold-Hopping
Miyazaki, R.; Takada, F.; Kikuchi, T.; Oguro, Y.; Kamata, M.; Yukawa, T.; Kato,K.; Muto, K.*; Yamaguchi, J.*
Chem. Sci. 2024, 15, 15835–15840. DOI: 10.1039/D4SC03874F
(48) Versatile deacylative cross-coupling of aromatic ketones
Nakahara, H.; Isshiki, R.; Iizumi, K.; Kubo, M.; Muto, K.; Yamaguchi, J.*
Chem 2024, 10, 2916–2930..
DOI: 10.1016/j.chempr.2024.07.002
(See also: ChemRxiv 2024, DOI: 10.26434/chemrxiv-2023-jx26c)
(47) Cine-Substitution of Enolates: Enolate Dance/Coupling of Cycloalkenyl Pivalates by Nickel Catalysis
Moriya, E.; Muto, K.; Yamaguchi, J.*
ACS Catal. 2024, 14, 10412–10417.
DOI:10.1021/acscatal.4c02707
(See also: ChemRxiv 2024, DOI: 10.26434/chemrxiv-2024-37kvr)
(46) Palladium-Catalyzed Denitrative Synthesis of Aryl Nitriles from Nitroarenes and Organocyanides
Iizumi, K.; Tanaka, H.; Muto, K.; Yamaguchi, J.*
Org. Lett. 2024, 13, e202300548.
DOI: 10.1021/acs.orglett.4c01118
(45) Pd-Catalyzed Cyclization/1,4-Difunctionalization of Bromoarenes with Diazo Compounds Leading to Bicyclic Skeletons
Fukuhara Y.; Kato, H.; Miyazaki, R.; Muto, K.*; Yamaguchi, J.*
Asian J. Org. Chem. 2023, 13, e202300548. (Invited contribution for Early Career Researcher Special Collection)
DOI: 10.1002/ajoc.202300548
(44) Concise Synthesis of (±)-Fortuneicyclidins and (±)-Cephalotine B Enabled by Pd-Catalyzed Dearomative Spirocyclization
Uwabe, Y.; Muto, K.*; Yamaguchi, J.*
Chem. Eur. J. 2023, 29, e202302769 (VIP paper) DOI: 10.1002/chem.202302769
Selected as a CoverArt DOI: 10.1002/chem.202303565
Highlighted in ChemistryViews
(See also: ChemRxiv 2023, DOI: 10.26434/chemrxiv-2023-jx26c)
(43) Chloroacetyl Boronate N-Tosylhydrazone as a Versatile Synthetic Building Block
Miyazaki, R.; Muto, K.*; Yamaguchi, J.*
Chem. Commun. 2023, 59, 7419-7422. (Open Access, Invited contribution for 2023 Emerging Investigators)
DOI: 10.1039/D3CC02086J
(See also: ChemRxiv 2023, DOI: 10.26434/chemrxiv-2023-5htqb)
(42) Pd-Catalyzed Denitriative Intramolecular Mizoroki–Heck Reaction
Asahara, K. K.; Muto, K.; Yamaguchi, J.*
Chem. Lett. 2023, 52, 299–302.
DOI: 10.1246/cl.230056
(41) Aryl Sulfide Synthesis via Aryl Exchange Reaction
Muto, K.; Isshiki, R.; Kurosawa, M. B.; Yamaguchi, J.*
Trends Chem. 2023, 5, 102–103.
DOI: 10.1016/j.trechm.2022.09.002
(40) Unified Synthesis of Multiply Arylated Alkanes by Catalytic Deoxygenative Transformation of Diarylketones
Kurosawa, M. B.; Kato, K.; Muto, K.; Yamaguchi, J.*
Chem. Sci. 2022, 13, 10743-10751.
DOI: 10.1039/D2SC03720C
(See also: ChemRxiv 2022, DOI: 10.26434/chemrxiv-2022-h1860)
(39) Synthesis and Properties of Palladium–Triazolopyridinylidene: Catalyst for Cross-Coupling Using Chloroarenes and Nitroarenes
Iizumi, K.; Nakayama, K. P.; Kato, K.; Muto, K.*; Yamaguchi, J.*
J. Org. Chem. 2022, 87, 11909–11918.
DOI: 10.1021/acs.joc.2c01562
(See also: ChemRxiv 2022, DOI 10.26434/chemrxiv-2022-qs9s9)
(38) Identification of α-Synuclein Proaggregator: Rapid Synthesis and Streamlining RT-QuIC Assays in Parkinson’s Disease
Takada, F.; Kasahara, T.; Otake, K.; Maru, T.; Miwa, M.; Muto, K.; Sasaki, M.; Hirozane, Y.; Yoshikawa, M.*; Yamaguchi, J.*
ACS Med. Chem. Lett. 2022, 13, 1421–1426.
DOI: 10.1021/acsmedchemlett.2c00138
Highlighted in Synfacts
(37) Pd-Catalyzed 1,4-Carboamination of Bicyclic Bromoarenes with Diazo Compounds and Amines
Wu, Q.; Muto, K.*; Yamaguchi, J.*
Org. Lett. 2022, 24, 4129–4134.
DOI: 10.1021/acs.orglett.2c01233
Most Read Article (Jul, 2022)
(See also: ChemRxiv 2022, DOI: 10.26434/chemrxiv-2022-s5vdz)
(36) Decarbonylative Reductive Coupling of Aromatic Esters by Nickel and Palladium Catalyst
Peng, Y.; Isshiki, R.; Muto, K.; Yamaguchi, J.*
Chem. Lett. 2022, 51, 749–753.
DOI: 10.1246/cl.220214
(See also: ChemRxiv 2022, DOI: 10.26434/chemrxiv-2022-s0sxl)
(35) Convergent Azaspirocyclization of Bromoarenes with N-Tosylhydrazones by a Palladium Catalyst
Yanagimoto, A.; Uwabe, Y.; Wu, Q.; Muto, K.*; Yamaguchi, J.*
ACS Catal. 2021, 11, 10429–10435.
DOI: 10.1021/acscatal.1c02627
Supplementary Cover, Most Read Article (Aug, 2021)
(See also: ChemRxiv 2021, DOI: 10.26434/chemrxiv.14762478)
(34) Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction
Isshiki, R.; Kurosawa, M. B.; Muto, K.; Yamaguchi, J.*
J. Am. Chem. Soc. 2021, 143, 10333–10340.
DOI: 10.1021/jacs.1c04215
Most Read Article (July, 2021), Press release (Japanese), Highlighted in newspaper
(see also: ChemRxiv 2021, DOI: 10.26434/chemrxiv.14462376)
(33) Decarbonylative Synthesis of Aryl Nitriles from Aromatic Esters and Organocyanides by a Nickel Catalyst
Iizumi, K.; Kurosawa, M. B.; Isshiki, R.; Muto, K.; Yamaguchi, J.*
Synlett 2021, 32, 1555–1559. (invited contribution)
DOI: 10.1055/s-0040-1705943
(32) Catalytic Three-component C–C Bond Forming Dearomatization of Bromoarenes with Malonates and Diazo Compounds
Kato, H.; Musha, I.; Komatsuda, M.; Muto, K.*; Yamaguchi, J.*
Chem. Sci. 2020, 11, 8779–8784.
DOI: 10.1039/D0SC02881A
(see also: ChemRxiv DOI: 10.26434/chemrxiv.12234740)
(31) Ester dance reaction on the aromatic ring
Matsushita, K.; Takise, R.; Muto, K.; Yamaguchi, J.*
Sci. Adv. 2020, 6, eaba7614.
DOI: 10.1126/sciadv.aba7614
(see also: ChemRxiv DOI: 10.26434/chemrxiv.11472264.v1)
(30) Catalytic Deoxygenative Coupling of Aromatic Esters with Organophosphorus Compounds
Kurosawa, B. M.; Isshiki, R.; Muto, K.; Yamaguchi, J.*
J. Am. Chem. Soc. 2020, 142, 7386–7392.
DOI: 10.1021/jacs.0c02839
(see also: ChemRxiv DOI: 10.26434/chemrxiv.11973585)
(29) Pd-Catalyzed C4-Dearomative Allylation of Benzyl Ammoniums with Allyltributylstannane
Kayashima, Y.; Komatsuda, M.; Muto, K.*; Yamaguchi, J.*
Chem. Lett. 2020, 49, 836–839.
DOI: 10.1246/cl.200216
Editor’s Choice, Top Accessed Article (2020 July), Inside Back Cover (Link)
(see also: ChemRxiv DOI: 10.26434/chemrxiv.12015663)
(28) Dearomative Allylation of Naphthyl Cyanohydrins by Palladium Catalysis: Catalyst-Enhanced Site Selectivity
Yanagimoto, A.; Komatsuda, M.; Muto, K.*; Yamaguchi, J.*
Org. Lett. 2020, 22, 3423–3427.
DOI: 10.1021/acs.orglett.0c00897
(see also: ChemRxiv DOI: 10.26434/chemrxiv.11961987)
(27) Palladium-Catalyzed Mizoroki–Heck Reaction of Nitroarenes and Styrene Derivatives
Okita, T.; Asahara, K. K.; Muto, K.; Yamaguchi, J.*
Org. Lett. 2020, 22, 3205–3208. (DOI: 10.1021/acs.orglett.0c00983)
(see also: ChemRxiv DOI: 10.26434/chemrxiv.11988516)
(26) Ester Transfer Reaction of Aromatic Esters with Haloarenes and Arenols by a Nickel Catalyst
Isshiki, R.; Inayama, N.; Muto, K.; Yamaguchi, J.*
ACS Catal. 2020, 10, 3490–3494.
DOI: 10.1021/acscatal.0c00291
Most Read Article (March, 2020), Press release (Japanese), Highlighted in newspaper (NikkeiSangyoShinbun)
(25) Pd-Catalyzed Alkenyl Thioether Synthesis from Thioesters and N-Tosylhydrazones
Ishitobi, K.; Muto, K.; Yamaguchi, J.*
ACS Catal. 2019, 9, 11685–11690
DOI: 10.1021/acscatal.9b04212
(24) Pd-Catalyzed Dearomative Three-Component Reaction of Bromoarenes with Diazo Compounds and Allylborates
Komatsuda, M.; Kato, H.; Muto, K*; Yamaguchi, J.*
ACS Catal. 2019, 9, 8991–8995.
DOI: 10.1021/acscatal.9b03461
Most Read Article (September, 2019)
(see also: ChemRxiv DOI: 10.26434/chemrxiv.8989130/1)
(23) Pd-Catalyzed Denitrative Intramolecular C–H Arylation
Asahara, K. K.; Okita, T.; Saito, A. N. Muto, K; Nakao, Y.; Yamaguchi, J.*
Org. Lett. 2019, 21, 4721–4724.
DOI: 10.1021/acs.orglett.9b01593
Most Read Article (July, 2019)
(22) Pd-Catalyzed Dearomative Allylation of Benzyl Phosphates
Komatsuda, M.; Muto, K.*; Yamaguchi, J.*
Org. Lett. 2018, 20, 4354–4357.
DOI: 10.1021/acs.orglett.8b01807
Most Read Article (August, 2018)
(21) Synthesis of A Heptaarylisoquinoline: Unusual Disconnection for Constructing Isoquinoline Frameworks
Asako, T.; Suzuki, S.; Itami, K.; Muto, K.; Yamaguchi, J.*
Chem. Lett. 2018, 47, 968–970.
DOI 10.1246/cl.180429
Highlights Editor’s Choice
(20) Dibenzofuran Synthesis: Decarbonylative Intramolecular C–H Arylation of Aromatic Esters
Okita, T.; Komatsuda, M.; Saito, A. N.; Hisada, T.; Takahara. T. T.; Nakayama, K. P.; Isshiki, R.; Takise, R.; Muto, K.; Yamaguchi, J.*
Asian J. Org. Chem. 2018, 7, 1358–1361. DOI 10.1002/ajoc.201800207
(19) Decarbonylative Methylation of Aromatic Esters by a Nickel Catalyst
Okita, T.; Muto, K.; Yamaguchi, J.*
Org. Lett. 2018, 20, 3132–3135. DOI 10.1021/acs.orglett.8b01233
(18) Pd-Catalyzed Decarbonylative C–H Coupling of Azoles and Aromatic Esters
Matsushita, K.; Takise, R.; Hisada, T.; Suzuki, S.; Isshiki, R.; Itami, K.; Muto, K.; Yamaguchi, J.*
Chem Asian. J. 2018, 13, 2393–2396. DOI: 10.1002/asia.201800478
(17) Decarbonylative Aryl Thioether Synthesis by Ni Catalysis
Ishitobi, K.; Isshiki, R.; Asahara, K. K.; Lim, C.; Muto, K.; Yamaguchi, J.*
Chem. Lett. 2018, 47, 756–759. DOI: 10.1246/cl.180226
(16) Decarbonylative C–P Bond Formation using Aromatic Esters and Organophosphorus Compounds
Isshiki, R.; Muto, K.; Yamaguchi, J.*
Org. Lett. 2018, 20, 1150–1153. DOI: 10.1021/acs.orglett.8b00080
(15) Catalytic α-Arylation of Ketones with Heteroaromatic Esters
Isshiki, R.; Takise, R.; Itami, K.; Muto, K.; Yamaguchi, J.*
Synlett 2017, 28, 2559–2603. DOI: 10.1055/s-0036-1589120
(14) Synthesis of Multiply Arylated Pyridines
Asako, T.; Hayashi, W.; Suzuki, S.; Amaike, K.; Itami, K.; Muto, K.; Yamaguchi, J.*
Tetrahedron 2017, 73, 3669–3676, (Invited contribution). DOI: 10.1016/j.tet.2017.03.095
(13) Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis
Takise, R.; Isshiki, R.; Muto, K.; Itami, K.*; Yamaguchi, J.*
J. Am. Chem. Soc. 2017, 139, 3340–3343. DOI: 10.1021/jacs.7b00049
Highly cited paper (Web of Science)
(12) Palladium-Catalyzed Decarbonylative Alkynylation of Aromatic Esters
Okita, T.; Kumazawa, K.; Takise, R.; Muto, K.; Itami, K.*; Yamaguchi, J.*
Chem. Lett. 2016, 46, 218–220. DOI: 10.1246/cl.161001
(11) Palladium-Catalyzed Decarbonylative Cross-Coupling of Azinecarboxylates with Arylboronic Acids
Muto, K.; Hatakeyama, T.; Itami, K.; Yamaguchi, J.*
Org. Lett. 2016, 18, 5106–5109. DOI: 10.1021/acs.orglett.6b02556
(10) C–H Arylation and Alkenylation of Imidazoles by Nickel Catalysis: Solvent accelerated Imidazole C–H Activation
Muto, K.; Hatakeyama, T.; Yamaguchi, J.; Itami, K.*
Chem. Sci. 2015, 6, 6792–6798. DOI: 10.1039/C5SC02942B
(9) C–H Activation Generates Period Shortening Molecules Targeting
Cryptochrome in the Mammalian Circadian Clock
Oshima, T.; Yamanaka, I.; Kumar, A.; Yamaguchi, J.; Nishiwaki-Ohkawa, T.; Muto, K.; Kawamura, R.; Hirota, T.; Yagita, K.; Irle, S.*; Kay, S. A.*; Yoshimura, T.*; Itami, K.*
Angew. Chem., Int. Ed. 2015, 54, 7193–7197. DOI: 10.1002/anie.201502942
(8) Decarbonylative Organoboron Cross-coupling of Esters by Nickel Catalysis
Muto, K.; Yamaguchi, J.*; Musaev, D. G.*; Itami, K.*
Nature Commun. 2015, 6, 7508. DOI: 10.1038/ncomms8508
Highlighted in Nature Asia.
Highly cited paper (Web of Science)
(7) Key Mechanistic Features of Ni-catalyzed C-H/C-O Biaryl Coupling of Azoles and Naphthalen-2-yl Pivalates
Xu, H.; Muto, K.; Yamaguchi, J.; Zhao, C.; Itami, K.*; Musaev, D. G.*
J. Am. Chem. Soc. 2014, 136, 14834–13844. DOI: 10.1021/ja5071174
(6) Nickel-Catalyzed α-Arylation of Ketones with Phenol Derivatives
Takise, R.; Muto, K.; Yamaguchi, J.*; Itami, K.*
Angew. Chem., Int. Ed. 2014, 53, 6791–6794. DOI: 10.1002/anie.201403823
(5) Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C-H/C-O Biaryl Coupling
Muto, K.; Yamaguchi, J.*; Lei, A.*; Itami, K.*
J. Am. Chem. Soc. 2013, 135, 16384–16387. DOI: 10.1021/ja409803x
(4) C–H Alkenylation of Azoles with Enols and Esters by Nickel Catalysis
Meng, L.; Kamada, Y.; Muto, K.; Yamaguchi, J.*; Itami, K.*
Angew. Chem., Int. Ed. 2013, 52, 10048–10051. DOI: 10.1002/anie.201304492
(3) Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to Synthesis of Muscoride A
Amaike, K.; Muto, K.; Yamaguchi, J.*; Itami, K.*
J. Am. Chem. Soc. 2012, 134, 13573–13576. DOI: 10.1021/ja306062c
Highly cited paper (Web of Science)
(2) Nickel-Catalyzed C–H/C–O coupling of Azoles with Phenol Derivatives
Muto, K.; Yamaguchi, J.; Itami, K.*
J. Am. Chem. Soc. 2012, 134, 169–172. DOI: 10.1021/ja210249h
Most Read Articles in JACS during December 2011
Highlighted as Synstory in Synform Highlighted in Newspapers (Chunichi, Yomiuri, Yahoo! News, Mynavi News and so on…)
Nagoya University Press Release
Highly cited paper (Web of Science)
(1) Nickel-Catalyzed C–H Arylation of Azoles with Haloarenes: Scope, Mechanism, and Applicationsto the Synthesis of Bioactive Molecules
Yamamoto, T.; Muto, K.; Komiyama, M.; Canivet, J.; Yamaguchi, J.; Itami, K.*
Chem. Eur. J. 2011, 17, 10113–10122. DOI: 10.1002/chem.201101091
Reviews
(10) 「パラジウム触媒によるベンジルおよびアリール求電子剤の脱芳香族的変換反応の開発」
Kato, H.; Muto, K.;* Yamaguchi, J.*
J. Synth. Org. Chem. Jpn. 2024, 82, 965–978. DOI: 10.5059/yukigoseikyokaishi.82.965 (Japanese)
(9) Development of Pd-Catalyzed Denitrative Couplings
Asahara, K. K.; Kashihara, M.; Muto, K.; Nakao, Y.; Yamaguchi, J.*
J. Synth. Org. Chem. Jpn. 2021, 79, 11–21. DOI: 10.5059/yukigoseikyokaishi.79.11.
(8) Transition-Metal-Catalyzed Denitrative Coupling of Nitroarenes
Muto, K.; Okita, T.; Yamaguchi, J.*
ACS Catal. 2020, 10, 9856–9871. DOI: 10.1021/acscatal.0c02990
Most Read Articles (2020)
(7) Decarbonylative Coupling Reaction of Aromatic Esters
Isshiki, R.; Okita, T.; Muto, K.; Yamaguchi, J.*
J. Synth. Org. Chem. Jpn. 2018, 76, 300–314. DOI: 10.5059/yukigoseikyokaishi.76.300 (Japanese)
(6) Synthesis of Fully Arylated (Hetero) arenes by Coupling Reaction
Asako, T.; Muto, K.; Yamaguchi, J.*
J. Synth. Org. Chem. Jpn. 2018, 76, 98–110. DOI: 10.5059/yukigoseikyokaishi.76.98 (Japanese)
(5) Cross-coupling of aromatic esters and amides”
Takise, R.; Muto, K.; Yamaguchi, J.*
Chem. Soc. Rev. 2017, 46, 5864–5888. DOI: 10.1039/C7CS00182G
Inside Back Cover DOI: 10.1039/C7CS90100C Highly cited paper (Web of Science)
(4) Catalytic Enantioselective Dihalogenation Reaction of Alkene
Kei Muto*
J. Synth. Org. Chem. Jpn. 2016, 74, 1225–1226. DOI: 10.5059/yukigoseikyokaishi.74.1225 (Japanese)
(3) “Nickel-Catalyzed Aromatic C–H Functionalization”
Yamaguchi, J.*; Muto, K.; Itami, K.*
Top. Curr. Chem, 2016, 374, 55. DOI:10.1007/s41061-016-0053-z
(2) “Nickel-Catalyzed Direct Coupling of Heteroarenes”
Yamaguchi, J.; Muto, K.; Amaike, K.; Yamamoto, T.; Itami, K.*
J. Synth. Org. Chem. Jpn. 2013, 71, 576–587. DOI: 10.5059/yukigoseikyokaishi.71.576 (Japanese)
(1) “Recent Progress in Nickel-Catalyzed Biaryl Coupling”
Yamaguchi, J.*; Muto, K.; Itami, K.*
Eur. J. Org. Chem. 2013, 19–30. DOI: 10.1002/ejoc.201200914
Highly cited paper (Web of Science)
Books and Others
(9) TBA (Pd-catalyzed dearomatization)
Muto, K.; Yamaguchi, J.
Science of Synthesis, in revision
(8) 「光で翻訳を制御する分子：ピューロスイッチ」
武藤慶, 日本薬学会 ファルマシア 2023, 59, 7, 679. (Link)
(7) Muto, K.; Yamaguchi, J. Cross-Coupling of Aromatic Esters by Decarbonylation. In Amide Bond Activation: Concepts and Reactions; Szostak, M., Ed.; Wiley-VCH, Weinheim, 2022; pp 453–486.
(6) 「有機合成のための新触媒反応101」 檜山爲次郎、野崎京子、中尾佳亮、中野幸司 編集
東京化学同人, 分担執筆 [項目54,55, 60, 71]
(5) 「武漢大学での武者修行」 (Japanese)
武藤慶, 近畿化学協会 有機金属部会 OMNews, 2021, 2, 38–39. (Link)
(4) Otsu Conference 2018 Reports 第9回大津会議 有機合成の夢を語る
Ikemoto, K.; Muto, K.; Nogi, K. J. Synth. Org. Chem. Jpn. 2018
(3) Lewis酸でヒドリドを引き抜く 触媒的FLPs形成によるC–H変換反応 (Japanese)
武藤慶, 化学 (化学同人), 2019年1月号
(2) Otsu Conference 2017 Reports 第8回大津会議 有機合成の夢を語る
Morita, M.; Ikemoto, K.; Muto, K. J. Synth. Org. Chem. Jpn. 2018
(1) ニッケル触媒を用いた新しいクロスカップリング反応とその応用
伊丹 健一郎, 山口 潤一郎, 天池 一真, 武藤 慶
(株) 技術情報協会 触媒の設計･反応制御 事例集 2013, 624–645.
Key Lectures
(17) 「TBA」◯武藤慶 日本化学会春季年会 2025 (招待講演)
(16) 「TBA」◯Kei Muto, Otsu-Conference Mini-Symposium, Osaka University, 2024/11/19 (Invited)
(15) 「未踏をいくことの楽しさ」◯武藤慶 長野県諏訪清陵高校 SSH講演会、長野、2024/8/22 (招待講演)
(14)「ベンジルパラジウムの変な反応性で遊ぶ有機合成」○武藤慶 南方研若手研究者セミナー、大阪大学吹田キャンパス 大阪、2024/5/18（招待講演）
(13)「ベンジルパラジウムの変な反応性で遊ぶ有機合成」 ○武藤慶 第11回慶應有機化学若手シンポジウム、慶應義塾大学日吉キャンパス、神奈川、2024/5/11（招待講演）
(12) “Multi-Dimensional Transformation of Arenes: Catalytic Dearomatization and Difunctionalization” ○武藤慶 名古屋大学ITbM、愛知、2024/4/15（招待講演）
(11) “Multi-Dimensional Transformation of Aromatic Compounds through Benzyl– Palladium” ○Kei Muto University of Southampton, UK、2023/12/15 (Invited Lecture)
(10)] “Multi-Dimensional Transformation of Aromatic Compounds through Benzyl– Palladium” ○Kei Muto University of Manchester, UK、2023/12/13 (Invited Lecture)
(9) “Multi-Dimensional Transformation of Aromatic Compounds through Benzyl– Palladium” ○Kei Muto Paris-Saclay University, France、202312/11 (Invited Lecture)
(8) “Multi-Dimensional Transformation of Aromatic Compounds through Benzyl– Palladium” ○Kei Muto Ecole Polytechnique, France、2023/12/8 (Invited Lecture)
(7) “Catalytic Dearomative Azaspirocyclization of Bromoarenes with N-Tosylhydrazones and Synthesis of Cephalotaxus Alkaloids” （Oral） ○Kei Muto, Yota Uwabe, Junichiro Yamaguchi The 15th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-15)（OP-19）、Rihga Royal Hotel Kyoto, Japan、2023/11/22
(6)「ベンジルパラジウム種を活かした触媒的な脱芳香族的官能基化」 ○武藤 慶 東京農工大学 招待講演、東京農工大学小金井キャンパス 東京、2022/12/16（招待講演）
(5) 「ベンジルパラジウムを鍵とする不活性芳香族の脱芳香族的官能基化」 ○武藤慶 日本化学会 第102春季年会 若い世代の特別講演（B201-3pm-05）、オンライン、2022/3/25（受賞講演）
(4) 「ベンジルパラジウム種を活かした触媒的脱芳香族的官能基化反応」 ○武藤 慶 第48回オルガノメタリックセミナー「効率的分子変換のフロンティア」、早稲田大学西早稲田キャンパス 東京、2021/11/20 (招待講演)
(3) “Organic Synthesis by Breaking Arenes: Development of Catalytic Dearomative Functionalization” ○Kei Muto Reaxys PhD Prize Virtual Symposium, Online, 2020/10/1 (招待講演)
(2) “Catalyst Design toward Selective Dearomative Functionalizations” MUTO, Kei 日本化学会第99春季年会 Special Program Lecture（4S3-06）、甲南大学岡本キャンパス 兵庫、2019/3/18 (招待講演)
(1)「C–O結合切断を起点とする新奇触媒反応の開発」 武藤慶 第2回 産総研化学研究シンポジウム、つくば、2018/10/12 (招待講演)