Takeuchi, J.; Iwamoto, T.; Watanabe, N.; Imoto, H.; Naka, K.
Polym. Chem.<\/em> 2026<\/strong>, in press.<\/p>\n\n\n\n
<\/p>\n\n\n\n
45. Study on the aggregation behavior of polyhedral oligomeric silsesquioxane compounds in solution<\/p>\n\n\n\n
Watanabe, N.; Iwamoto, T.; Imoto, H.; Naka, K.<\/p>\n\n\n\n
Bull. Chem. Soc. Jpn.<\/em> 2026<\/strong>, in press.<\/p>\n\n\n\n <\/p>\n\n\n\n 44. “Synthesis of Network Polymers Composed of Well-Defined Silyl Ether Macrocycles” <\/p>\n\n\n\n 43. “Latent One-Dimensional Luminescent Coordination Polymer Emerging from Copper(I) Iodide Secondary Building Units” <\/p>\n\n\n\n 42. “Homo- and co-polymers of cage silsesquioxane-tethered methacrylate and styryl monomers: Effects of linker length and rigidity on film transparency” <\/p>\n\n\n\n 41. “Cold crystallization of a macrocyclic molecule with semi-flexible silyl ether units”<\/p>\n\n\n\n Iwamoto, T.*; Amano, S.; Maeda, K.; Shibama, N.; Sekiguchi, W.; Imaizumi, A.; Honda, A.; Chang, H.-C.; Houjou, H.; Imoto, H.; Naka, K.; Ishii, Y.<\/p>\n\n\n\n J. Phys. Chem. B <\/em>2026<\/strong>, 130, <\/em>1724\u20131729.<\/p>\n\n\n\n <\/p>\n\n\n\n 40. \u201cSupramolecular Polymer Materials Assembled via Polymerization and Subsequent Crosslinking through a Single Hydrogen-Bonding Motif\u201d<\/p>\n\n\n\n Takeuchi, J.; Iwamoto, T.; Imoto, H.; Naka, K.*<\/p>\n\n\n\n Macromolecules<\/em> 2026<\/strong>, 59<\/em>, 1014\u20131022.<\/p>\n\n\n\n <\/p>\n\n\n\n 39. \u201cPoly(methacrylate)s of cage silsesquioxanes with hydrogen bonding networks toward optically transparent films\u201d<\/p>\n\n\n\n Nagashima, C.; Iwamoto, T.; Naka, K.; Imoto, H.*<\/p>\n\n\n\n J. Polym. Sci.<\/em> 2026<\/strong>, 64<\/em>, 734\u2013742.<\/p>\n\n\n\n <\/p>\n\n\n\n 38. \u201cStructural Effects of Arsine Ligands on C\u2013H Difunctionalization of Thiophene\u201d<\/p>\n\n\n\n Sumida, A.; Yamamoto, K.; Iwamoto, T.; Naka, K.; Imoto, H.*<\/p>\n\n\n\n Chem. Sci.<\/em> 2025<\/strong>, 16<\/em>, 20843\u201320850.<\/p>\n\n\n\n <\/p>\n\n\n\n 37. \u201cSurface segregation behavior of octaalkoxy-substituted cage octasilsesquioxanes in poly(methyl methacrylate)\u201d<\/p>\n\n\n\n Okamura, N.; Takeuchi, J.; Iwamoto, T.; Imoto, H.; Naka, K.*<\/p>\n\n\n\n Bull. Chem. Soc. Jpn.<\/em> 2025<\/strong>, 98<\/em>, uoaf094.<\/p>\n\n\n\n <\/p>\n\n\n\n <\/p>\n\n\n\n 36. \u201cCopolymerization of cage silsesquioxanes with different substituents for inhibition of side-chain crystallization\u201d<\/p>\n\n\n\n Nagashima, C.; Tomioka, Y.; Tanaka, R.; Iwamoto, T.; Naka, K.; Imoto, H.*<\/p>\n\n\n\n Macromol. Chem. Phys.<\/em> 2025<\/strong>, 226<\/em>, e00237.<\/p>\n\n\n\n <\/p>\n\n\n\n 35. “Exclusive macrocyclization through multiple Si\u2013O bond formations from diol and dichlorosilane”<\/p>\n\n\n\n Iwamoto, T.*; Amano, S.; Maeda, K.; Shibama, N.; Sekiguchi, W.; Kazama, Y.; Nakamura, Y.; Sugamata, K.; Imoto, H.; Naka, K.; Ishii, Y.<\/p>\n\n\n\n Chem. Commun.<\/em> 2025<\/strong>, 61<\/em>, 8180\u20138183. (Front Cover\u306b\u63a1\u7528<\/strong>)<\/p>\n\n\n\n <\/p>\n\n\n\n 34. \u201cCombination of Arsines and Tris(pentafluorophenyl)borane towards Frustrated Lewis Pair\u201d<\/p>\n\n\n\n Onishi, T.; Sumida, A.; Okochi, C.; Miyake, Y.; Kanaori, K.; Iwamoto, T.; Naka, K.; Imoto, H.<\/p>\n\n\n\n Chem. Eur. J.<\/em> 2025<\/strong>, 31<\/em>, e202501086.<\/p>\n<\/div>\n\n\n\n <\/p>\n\n\n\n 33. “Post-Synthetic Modification of Calix[4]arene Framework by Iridium\u2013Mediated Alkyne Insertion into an Inert C\u2212C Bond: A Novel Strategy for Unsymmetrical Macrocycles” <\/p>\n\n\n\n 32. \u201dVinylidene Rearrangements of Internal Borylalkynes via 1,2-Boryl Migration”<\/p>\n\n\n\n Iwamoto, T.*; Mitsubo, K.; Sakajiri,Y.; Ishii, Y.*<\/p>\n\n\n\n Dalton Trans.<\/em> 2024<\/strong>, 53<\/em>, 9715\u20139723.<\/p>\n\n\n\n <\/p>\n\n\n\n 31. \u201cOne-pot Syntheses of Benzo- and Benzofuran-fused Iridaoxabenzenes via CH Bond Activations of Alkyl-bridged Diphenol Derivatives\u201d<\/p>\n\n\n\n Iwamoto, T.*; Suzuki, M.; Hasegawa, H.; Abeta, H.; Matsuo, Y.; Tanaka, T.; Yasuda, N.; Ishii, Y.*<\/p>\n\n\n\n Chem. Asian. J. 2023, e202300640.<\/p>\n\n\n\n <\/p>\n\n\n\n 30. \u201cBinuclear Complexes Supported by a Tetrapyridyl Ligand with a Bending Anthraquinodimethane Linker\u201d<\/p>\n\n\n\n Iwamoto, T.*; Sotome, Y.; Ishii, Y.*<\/p>\n\n\n\n ACS Organic & Inorganic Au, 2023, 305\u2013311.<\/p>\n\n\n\n <\/p>\n\n\n\n 29. \u201cRetro-Vinylidene Rearrangements of P- and S-Substituted Ruthenium Vinylidene Complexes\u201d<\/p>\n\n\n\n Iwamoto, T.*; Saito, K.; Mitsubo, T.; Kuwabara, T.; Ishii, Y.*<\/p>\n\n\n\n Organometallics 2023, 42, 167\u2013173.<\/p>\n\n\n\n <\/p>\n\n\n\n 28. \u201cExperimental Observation of \u03b2-Carbon Elimination from Alkenylrhodium Complexes through Exchange Reactions of the Alkenyl Unit\u201d<\/p>\n\n\n\n Iwamoto, T.; Shibuya, K.; Takakuwa, T.; Kuwabara, T.; Ishii, Y.*<\/p>\n\n\n\n Organometallics 2022, 41, 182\u2013186.<\/p>\n\n\n\n <\/p>\n\n\n\n 27. \u201cDevelopment of P- and N-Chirogenic Ligands Based on Chiral Induction from a Phosphorus Donor to a Nitrogen Donor in Palladium Complexes\u201d<\/p>\n\n\n\n Iwamoto, T.*; Mizuhata, Y.; Tokitoh, N.; Nakamura, M. <\/p>\n\n\n\n Organometallics 2020, 39, 1672\u20131677.<\/p>\n\n\n\n <\/p>\n\n\n\n <\/em>26. \u201cEndergonic Addition of N-Methylamines to Aromatic Ketones Driven by Photochemical Offset of the Entropic Cost\u201d 25. \u201cIron-Catalysed Enantioselective Suzuki\u2013Miyaura Coupling of Racemic Alkyl Bromides\u201d <\/p>\n\n\n\n 24. \u201cIron-Catalyzed Cross Coupling of Aryl Chlorides with Alkyl Grignard Reagents: Synthetic scope and FeII\/FeIV mechanism supported by X-ray absorption spectroscopy and density functional theory calculations\u201d <\/p>\n\n\n\n 23. \u201cDFT and AFIR Study on the Mechanism and the Origin of Enantioselectivity in Iron-Catalyzed Cross-Coupling Reactions\u201d <\/p>\n\n\n\n 22. \u201d Iron-Catalyzed anti-Selective Carbosilylation of Internal Alkynes\u201d <\/p>\n\n\n\n 21. \u201dShortest Double-Walled Carbon Nanotubes Composed of Cycloparaphenylenes\u201d <\/p>\n\n\n\n 20. \u201cONO-pincer ruthenium complex-bound norvaline for efficient catalytic oxidation of methoxybenzenes with hydrogen peroxide\u201d <\/p>\n\n\n\n 19. \u201cLigand-controlled Synthesis of [3]- and [4]Cyclo-9,9-dimethyl-2,7-fluorenes through Triangle- and Square-shaped Platinum Intermediates\u201d <\/p>\n\n\n\n 18. \u201cRadical Ions of Cyclopyrenylene: Comparison of Spectral Properties with Cycloparaphenylene.\u201d <\/p>\n\n\n\n 17. \u201cIron(III) Fluoride\/N-Heterocyclic Carbene Catalyzed Cross Coupling between Deactivated Aryl Chlorides and Alkyl Grignard Reagents with or without b-Hydrogens\u201d <\/p>\n\n\n\n 16. \u201cInvestigation of Organoiron Catalysis in Kumada\u2013Tamao\u2013Corriu-Type Cross-Coupling Reaction Assisted by Solution-Phase X-ray Absorption Spectroscopy\u201d <\/p>\n\n\n\n 15. \u201cPartial Charge Transfer in Shortest Possible Metallofullerene Peapod, La@C82\u2e26[11]Cycloparaphenylene.\u201d <\/p>\n\n\n\n 14. \u201cChameleon-like Behaviour of Cyclo[n]paraphenylenes in Complexes with C70. On Their Impressive Electronic and Structural Adaptability as probed By Raman spectroscopy.\u201d <\/p>\n\n\n\n 13. \u201cRadical Ions of Cycloparaphenylenes: Size-Dependence Contrary to the Neutral Molecules\u201d <\/p>\n\n\n\n 12. \u201cProperties of Triplet-Excited [n]Cycloparaphenylenes (n = 8-12): Excitation Energies Lower than Those of Linear Oligomers and Polymers\u201d <\/p>\n\n\n\n 11. \u201cSynthesis, Characterization, and Properties of [4]Cyclo-2,7-pyrenylene: Effect of Cyclic Structure on the Electronic Properties of Pyrene Oligomers\u201d <\/p>\n\n\n\n 10. \u201cProperties of Sizeable [n]Cycloparaphenylenes as Molecular Models of Single-Wall Carbon Nanotubes Elucidated by Raman Spectroscopy: Structural and Electron-Transfer Responses under Mechanical Stress\u201d <\/p>\n\n\n\n 9. \u201cElectron Transfer in a Supramolecular Associate of a Fullerene Fragment\u201d <\/p>\n\n\n\n 8. \u201cSynthesis and Physical Properties of a Ball-Like Three-Dimensional \uf070-Conjugated Molecule\u201d <\/p>\n\n\n\n 7. \u201cSize- and Orientation-Selective Encapsulation of C70 by Cycloparaphenylenes\u201d <\/p>\n\n\n\n 6. \u201cSelective Synthesis of [6]-, [8]-, and [10]Cycloparaphenylenes\u201d <\/p>\n\n\n\n 5. \u201cEnhancement of Quinoidal Character of Smaller [n]Cycloparaphenylenes Probed by Raman Spectroscopy\u201d <\/p>\n\n\n\n 4. \u201cSize-Dependent Fluorescence Properties of [n]Cycloparaphenylenes (n =8-13), Hoop-Shaped \u03c0-Conjugated Molecules\u201d <\/p>\n\n\n\n 3. \u201cSize-Selective Encapsulation of C60 by [10]Cycloparaphenylene: Formation of the Shortest Fullerene-Peapod\u201d <\/p>\n\n\n\n 2. \u201cSelective and Random Syntheses of [n]Cycloparaphenylenes (n = 8-13) and Size Dependence of Their Electronic Properties\u201d <\/p>\n\n\n\n 1. \u201cSynthesis of [8]Cycloparaphenylene from a Square-Shaped Tetranuclear Platinum Complex\u201d <\/p>\n\n\n\n 8. \u201cVinylidene Complexes\u201d\u3000 <\/p>\n\n\n\n 7. \u201cIron-Catalyzed Enantioselective Cross-Coupling Reactions for the Synthesis of Propionic Acid Anti-inflammatory Compounds\u201d <\/p>\n\n\n\n 5. \u201cMetalated Amino Acids and Peptides: A Key Functional Platform for Applications to Controlled Metal Array Fabrication and Supramolecular Catalysts\u201d <\/p>\n\n\n\n 4. \u300c\u5149\u89e6\u5a92\u304c\u62d3\u304f\u70ad\u7d20\u8cc7\u6e90\u306e\u5206\u5b50\u5909\u63db-\u4e8c\u9178\u5316\u70ad\u7d20\u306e\u4e00\u96fb\u5b50\u9084\u5143\u3092\u8d77\u70b9\u3068\u3059\u308b\u30ab\u30eb\u30dc\u30ad\u30b7\u30eb\u5316\u53cd\u5fdc\u300d <\/p>\n\n\n\n 3. \u201cOrganoplatinum-Mediated Synthesis of Cyclic \u03c0-Conjugated Molecules: Towards a New Era of Three-Dimensional Aromatic Compounds\u201d <\/p>\n\n\n\n 2. \u201cStructural Investigation of Cycloparaphenylene \u2013Fullerene Supramolecular Complexes Using Synchrotron Radiation and Theoretical Calculation\u201d <\/p>\n\n\n\n 1. \u201cNew Organic Chemistry of Three-Dimensional \u03c0-Conjugated Compounds\u201d <\/p>\n","protected":false},"excerpt":{"rendered":" \u3053\u308c\u307e\u3067\u306e\u7814\u7a76\u696d\u7e3e\uff08\u539f\u8457\u8ad6\u6587\u3001\u7dcf\u8aac\uff09 \u539f\u8457\u8ad6\u6587 46. Stereochemically Purified trans-Dihydroxy-Substituted Cage Silsesquioxane-Based Bi […]<\/p>\n","protected":false},"author":2,"featured_media":210,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-18","page","type-page","status-publish","has-post-thumbnail","hentry"],"_links":{"self":[{"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/pages\/18","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=18"}],"version-history":[{"count":36,"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/pages\/18\/revisions"}],"predecessor-version":[{"id":303,"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/pages\/18\/revisions\/303"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=\/wp\/v2\/media\/210"}],"wp:attachment":[{"href":"https:\/\/kit-synth-lab.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=18"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Amano, A.; Nakai, C.; Sugamata, K.; Watanabe, N.; Imoto, H.; Naka, K.; Iwamoto, T.*
Polym. Chem.<\/em> 2026<\/strong>, 17<\/em>, 1162\u20131166. (Front Cover\u306b\u63a1\u7528<\/strong>)<\/p>\n\n\n\n![\"\"](\"https:\/\/kit-synth-lab.com\/wp-content\/uploads\/2026\/04\/image.png\")
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Kikuchi, K.; Nagata, S.; Yumura, T.; Iwamoto, T.; Naka, K.; Imoto, H.*
Inorg. Chem. Front.<\/em> 2026<\/strong>, advanced article.<\/p>\n\n\n\n![\"\"](\"https:\/\/kit-synth-lab.com\/wp-content\/uploads\/2026\/03\/image.png\")
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Nagashima, C.; Iwamoto, T.; Naka, K.; Imoto, H.*
Chem. Lett.<\/em> 2026<\/strong>, 55, upag018.<\/p>\n\n\n\n![\"\"](\"https:\/\/kit-synth-lab.com\/wp-content\/uploads\/2026\/03\/image-1.png\")
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Iwamoto, T.*; Hasegawa, H.; Mori, D.; Yamazaki, T.; Fujinuki, K.; Ishii, Y.*
Chem. Eur. J. <\/em>2024<\/strong>, 30<\/em>, e202401490.<\/p>\n\n\n\n![\"\"](\"https:\/\/kit-synth-lab.com\/wp-content\/uploads\/2025\/10\/chem202401490-toc-0001-m.jpg\")
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Iwamoto, T.*; Hosokawa, A.; Nakamura, M.*
Chem. Commun. 2019, 55, 11683\u201311686. <\/p>\n\n\n\n
Iwamoto, T.; Okuzono, C.; Adak, L.; Jin, M.; Nakamura, M.*
Chem. Commun. 2019, 55, 1128\u20131131. <\/p>\n\n\n\n
Agata, R.; Takaya, H.; Matsuda, H.; Nakatani, N.; Takeuchi, K.; Iwamoto, T.; Hatakeyama, T.; Nakamura, M.*
Bull. Chem. Soc. Jpn. 2019, 92, 381\u2013390. <\/p>\n\n\n\n
Sharma, A. K.; Sameera, W. M. C.; Jin, M.; Adak, L.; Okuzono, C.; Iwamoto, T.; Kato, M.; Nakamura, M.; Morokuma, K.
J. Am. Chem. Soc. 2017, 139, 16117\u201316125. <\/p>\n\n\n\n
Iwamoto, T.; Nishikori, T.; Nakagawa, N.; Takaya, H.; Nakamura, M.*
Angew. Chem. Int. Ed. 2017, 56, 13298\u201313301.<\/p>\n\n\n\n
Hashimoto, S.; Iwamoto, T.; Kurachi, D.; Kayahara, E.; Yamago, S.*
ChemPlusChem 2017, 82, 1015\u20131020. <\/p>\n\n\n\n
Yoshida, R.; Isozaki, K.; Yokoi, T.; Yasuda, N.; Sadakane, K; Iwamoto, T.; Takaya, H.; Nakamura. M.
Org. Biomol. Chem. 2016, 14, 7468\u20137479. <\/p>\n\n\n\n
Kayahara, E; Qu, R.; Kojima, M.; Iwamoto, T.; Suzuki, T.; Yamago, S.*
Chem. Eur. J. 2015, 21, 18939\u201318943.<\/p>\n\n\n\n
Fujistuka, M.; Tojo, S.; Iwamoto, T.; Kayahara, E.; Yamago, S.; Majima, T.
J. Phys. Chem. Part A 2015, 119, 4136\u20134141.<\/p>\n\n\n\n
Agata, R.; Iwamoto, T.; Nakagawa, N.; Isozaki, K.; Hatakeyama, T.; Takaya, H.; Nakamura. M.*
Synthesis 2015, 47, 1733\u20131740. <\/p>\n\n\n\n
Takaya, H.; Nakajima, S.; Nakagawa, N.; Isozaki, K.; Iwamoto, T.; Imayoshi, R.; Gower, N. J.; Adak, L.; Hatakeyama, T.; Honma, T.; Takagaki, M.; Sunada, Y.; Nagashima, H.; Hashizume, D.; Takahashi, O.; Nakamura. M.*
Bull. Chem. Soc. J. 2015, 20, 14403\u201314409.<\/p>\n\n\n\n
Iwamoto, T.; Slanina, Z.; Mizorogi, N.; Guo, J.; Akasaka, T.; Nagase, S.; Takaya, H.; Yasuda, N.; Kato, T.; Yamago, S.*
Chem. Eur. J. 2014, 20, 14403\u201314409.<\/p>\n\n\n\n
Pe\u00f1aAlvarez, M.; Burrezob, P. M.; Iwamoto, T.; Taravilloa, M.; Baonzaa, V. G.; Navarreteb, J. T. L.; Yamago, S.; Casado, J.*
Faraday Discussion 2014, 173, 157\u2013171.<\/p>\n\n\n\n
Fujitsuka, M.; Tojo, S.; Iwamoto, T.; Kayahara, E.; Yamago, S.; Majima, T.
J. Phys. Chem. Lett. 2014, 5, 2302\u20132305.<\/p>\n\n\n\n
Fujitsuka, M.; Lu, C.; Iwamoto, T.; Kayahara, E.; Yamago, S.; Majima, T.
J. Phys. Chem. A 2014, 118, 4527\u20134532.<\/p>\n\n\n\n
Iwamoto, T.; Kayahara, E.; Yasuda, N.; Suzuki, T.; Yamago, S.*
Angew. Chem. Int. Ed. 2014, 53, 6430\u20136434. <\/p>\n\n\n\n
Alvarez, M. P.; Burrezo, P. M.; Kertesz, M.; Iwamoto, T.; Yamago, S.; Xia, J.; Jasti, R.; Navarrete, J. T. L.; Taravillo, M.; Baonza, V. G.; Casado, J.*
Angew. Chem. Int. Ed. 2014, 53, 7033\u20137037. <\/p>\n\n\n\n
Gallego, M.; Calbo, J.; Arag\u00f3, , J.; Krick Calderon, R. M.; Liquido, F. H.; Iwamoto, T.; Greene, A. K.; Jackson, E. A.; P\u00e9rez, E. M.; Ort\u00ed, E.; Guldi, D. M.; Scott, L. T.; Mart\u00edn, N.*
Angew. Chem. Int. Ed. 2014, 53, 2170\u20132175. <\/p>\n\n\n\n
Kayahara, E.; Iwamoto, T.; Takaya, H.; Suzuki, T.; Fujitsuka, M.; Majima, T.; Yasuda, N.; Matsuyama, N.; Seki, S.; Yamago, S.*
Nature Commun. 2013, 4, 2694.<\/p>\n\n\n\n
Iwamoto, T.; Watanabe, Y.; Takaya, H.; Haino, T.; Yasuda, N.; Yamago, S.*
Chem. Eur. J. 2013, 19, 14061\u201314068. <\/p>\n\n\n\n
Kayahara, E.; Iwamoto, T.; Suzuki, T.; Yamago, S.*
Chem. Lett. 2013, 42, 621\u2013623. <\/p>\n\n\n\n
Fujitsuka, M.; Iwamoto, T.; Kayahara, E.; Yamago, S.; Majima, T.
ChemPhysChem. 2013, 14, 1570\u20131572. <\/p>\n\n\n\n
Fujitsuka, M.; Cho, D. W.; Iwamoto, T.; Yamago, S.; Majima, T.
Phys. Chem. Chem. Phys. 2012, 14, 14585\u201314588. <\/p>\n\n\n\n
Iwamoto, T.; Watanabe, Y.; Sadahiro, T.; Haino, T.; Yamago, S.*
Angew. Chem. Int. Ed. 2011, 50, 8342\u20138344. <\/p>\n\n\n\n
Iwamoto, T.; Watanabe, Y.; Sakamoto, Y.; Suzuki, T.; Yamago, S.*
J. Am. Chem. Soc. 2011, 133, 8354\u20138361. <\/p>\n\n\n\n
Yamago, S.*; Watanabe, Y.; Iwamoto, T.
Angew. Chem. Int. Ed. 2010, 49, 757\u2013759.<\/p>\n\n\n\n\u7dcf\u8aac\u3001\u89e3\u8aac\u8a18\u4e8b<\/h2>\n\n\n\n
Iwamoto, T.; Ishii, Y.
Encyclopedia of Inorganic and Bioorganic Chemistry, 2022.<\/p>\n\n\n\n
Nakamura, M.; Iwamoto, T.; Jin, M.; Okuzono, C.
Chemical Times, 2021, 1, 13\u201319.<\/p>\n\n\n\n
Takaya, H.; Isozaki, K.; Yokoi, T.; Ogata, K.; Shanoh, T.; Yasuda, N.; Iwamoto, T.; Nakamura, M.
Journal of Synthetic Organic Chemistry Japan 2019, 76, 1010\u20131023.<\/p>\n\n\n\n
\u5316\u5b66\u30012018, 73, 70\u201371.\u3000\u5316\u5b66\u540c\u4eba<\/p>\n\n\n\n
Yamago, S.; Kayahara, E.; Iwamoto, T.
Chem. Rec. 2014, 14, 84\u2013100.<\/p>\n\n\n\n
Iwamoto, T.; Takaya, H.; Yamago, S.
Nihon Kessho Gakkaishi, 2015, 57, 239\u2013244.<\/p>\n\n\n\n
Yamago, S.; Kayahara, E.; Iwamoto, T.
Journal of Synthetic Organic Chemistry, Japan. 2014, 72, 992-1005.<\/p>\n\n\n\n