{"id":16,"date":"2024-02-09T11:01:11","date_gmt":"2024-02-09T02:01:11","guid":{"rendered":"https:\/\/www.lbb.iir.isct.ac.jp\/MedOrgChem\/?page_id=16"},"modified":"2026-04-08T12:27:27","modified_gmt":"2026-04-08T03:27:27","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.lbb.iir.isct.ac.jp\/MedOrgChem\/publications\/","title":{"rendered":"\u7814\u7a76\u696d\u7e3e"},"content":{"rendered":"\n

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  1. Cationic iridium-catalyzed enantioselective decarboxylative aryl addition of aromatic carboxylic acids to bicyclic alkenes<\/strong>
    R. Asano, R. Nonami, H. Hamasaki, K. Kanemoto, H. Fujita, K. Yamamoto, T. Seki, K. Shibatomi, S. Kuwahara, T. Shirai*
    Chem. Commun.<\/em> 2026<\/strong>, in press<\/em>.  DOI: 10.1039\/D6CC00389C<\/a>
    \u3010Inside Front Cover\u3011<\/li>\n\n\n\n
  2. Dithiofunctionalization: a versatile approach for constructing complex disulfides from alkenes and alkynes<\/strong>
    Y. Takami, E. Kwon, K. Kanemoto*
    Org. Chem. Front.<\/em> 2026<\/strong>, 13<\/em>, 1299.  DOI:     10.1039\/D5QO01625H<\/a>
    \"\"<\/li>\n\n\n\n
  3. Precision synthesis of peptide chimeras through site-specific azomethine ylide\u2013dehydroalanine cycloaddition<\/strong>
    M. Iwata, Y. Takami, S. Miura, H. Ohno, E. Kwon, N. Yoshikai, K. Kanemoto*
    Org. Chem. Front.<\/em> 2026<\/strong>, 13<\/em>, 1317.  DOI:     10.1039\/D5QO01627D<\/a>
    \"\"<\/li>\n\n\n\n
  4. Preparation of Unsymmetrical Disulfides via Catalytic Lewis Base Activation of N<\/em>-(Organodithio)phthalimides<\/strong>
    H. Ohno, Y. Takami, K. Kanemoto*
    J. Org. Chem.<\/em> 2026<\/strong>, 91<\/em>, 1817.  DOI:     10.1021\/acs.joc.5c03056<\/a>
    \"\"<\/li>\n\n\n\n
  5. Formal Cyclopropylation of Imines with Cyclopropanols: Stereocontrolled Access to Conformationally Constrained \u03b3-Amino Alcohols<\/strong>
    K. Tsukiji, K. Kanemoto, E. Kwon, N. Yoshikai*
    Angew. Chem. Int. Ed.<\/em> 2025<\/strong>, 64<\/em>, e202511646.  DOI:     10.1002\/anie.202511646<\/a><\/li>\n\n\n\n
  6. Hexadehydro Diels\u2013Alder\/Alkynyliodanation Cascade: A Highly Regioselective Entry to Polycyclic Aromatics<\/strong>
    S. Morohashi, L. Zhou, K. Kanemoto*, E. Kwon, N. Yoshikai*
    Org. Lett.<\/em> 2025<\/strong>, 27<\/em>, 4269.  DOI:     10.1021\/acs.orglett.5c00956<\/a><\/li>\n\n\n\n
  7. Diazomethyl-\u03bb3<\/sup>-iodane Meets Aryne: Dipolar Cycloaddition and C-to-N Iodane Shift Leading to Indazolyl-\u03bb3<\/sup>-iodanes<\/strong>
    S. Otsuki, K. Kanemoto,* D. C. Martos, E. Kwon, J. Wencel-Delord, N. Yoshikai*
    Chem. Sci.<\/em> 2025<\/strong>, 16<\/em>, 8053.  DOI:     10.1039\/D5SC00266D<\/a><\/li>\n\n\n\n
  8. A versatile entry to unnatural, disulfide-linked amino acids and peptides through the disulfuration of azlactones<\/strong>
    M. Iwata, Y. Takami, H. Asanuma, K. Hosono, H. Ohno, N. Yoshikai, K. Kanemoto*
    Chem. Sci.<\/em> 2025<\/strong>, 16<\/em>, 2777.  DOI:     10.1039\/D4SC07187E<\/a>
    \u3010    \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/a>\u3011\u3010\u65e5\u7d4c\u65b0\u805e\u96fb\u5b50\u7248<\/a>\u3011\u3010\u65e5\u520a\u5de5\u696d\u65b0\u805e\u3011\u3010Highlighted in Synfacts<\/em>, 2025<\/strong>, 21<\/em>, 429.\u3011
    \"\"<\/li>\n\n\n\n
  9. Stereoselective Hydroxyallylation of Cyclopropenes with Cyclopropanols via NHC Catalysis of Transient Organozinc Species<\/strong>
    K. Tsukiji, A. Matsumoto, K. Kanemoto,* N. Yoshikai*
    Angew. Chem. Int. Ed.<\/em> 2024<\/strong>, 63<\/em>, e202412456.  DOI:     10.1002\/anie.202412456<\/a>
    \u3010    Chem-Station \u30b9\u30dd\u30c3\u30c8\u30e9\u30a4\u30c8\u30ea\u30b5\u30fc\u30c1<\/a>\u3011<\/li>\n\n\n\n
  10. N\u2010Terminal\u2010Specific Dual Modification of Peptides through Copper\u2010Catalyzed [3+2] Cycloaddition<\/strong>
    H. Machida, K. Kanemoto*
    Angew. Chem. Int. Ed.<\/em> 2024<\/strong>, 63<\/em>,e202320012.  DOI:     10.1002\/anie.202320012<\/a>
    \u3010    \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/a>\u3011\u3010\u65e5\u7d4c\u65b0\u805e\u96fb\u5b50\u7248<\/a>\u3011\u3010Chem-Station \u30b9\u30dd\u30c3\u30c8\u30e9\u30a4\u30c8\u30ea\u30b5\u30fc\u30c1<\/a>\u3011
    \"\"<\/li>\n\n\n\n
  11. Carboiodanation of Arynes: Organoiodine(III) Compounds as Nucleophilic Organometalloids<\/strong>
    C. Arakawa,+<\/sup> K. Kanemoto,+<\/sup> K. Nakai, C. Wang, S. Morohashi, E. Kwon, S. Ito, N. Yoshikai*
    +<\/sup>Equal contribution.
    J. Am. Chem. Soc.<\/em> 2024<\/strong>, 146<\/em>, 3910.  DOI:     10.1021\/jacs.3c11524<\/a><\/li>\n\n\n\n
  12. Construction of Diverse Pyrrolidine-Based Skeletons through Ag-Catalyzed Stereoselective Addition\u2013Elimination Reaction of Azomethine Ylides with Nitroallyl Acetates<\/strong>
    I. Ohno, K. Kanemoto*, S. Furuya, Y. Suzuki, S.-i. Fukuzawa*
    Org. Lett.<\/em> 2024<\/strong>, 26<\/em>, 1880.  DOI:     10.1021\/acs.orglett.4c00184<\/a>
    \"\"<\/li>\n\n\n\n
  13. Amino- and Alkoxybenziodoxoles: Facile Preparation and Use as Arynophiles<\/strong>
    K. Kanemoto, K. Yoshimura, K. Ono, W. Ding, S. Ito, N. Yoshikai*
    Chem. Eur J. <\/em>2024<\/strong>, 30<\/em>, e202400894.  DOI:     10.1002\/chem.202400894<\/a><\/li>\n\n\n\n
  14. Amination of N<\/em>-(Organodithio)phthalimides for the Modular Synthesis of Aminodisulfides<\/strong>
    H. Asanuma, K. Kanemoto* Org. Lett.<\/em> 2024<\/strong>, 26<\/em>, 438.\u00a0 DOI:     10.1021\/acs.orglett.3c03419<\/a>
    \u3010Selected as Front Cover\u3011
    \"\"<\/li>\n\n\n\n
  15. Dipolarophile-Steered Formal Stereodivergent Synthesis of 2,5-cis<\/em>\/trans<\/em>-Pyrrolidines Based on Asymmetric 1,3-Dipolar Cycloaddition of Imino Lactones<\/strong>
    S. Furuya, K. Muroi, K. Kanemoto, S.-i. Fukuzawa*
    Chem. Eur. J.<\/em> 2023<\/strong>, 29<\/em>, e202302609.  DOI:     10.1002\/chem.202302609<\/a><\/li>\n\n\n\n
  16. Cationic Iridium\u2010Catalyzed Decarboxylation of Aromatic Carboxylic Acids<\/strong>
    R. Nonami, Y. Kishino, T. Yamasaki, K. Kanemoto, K. Iwai, N. Nishiwaki, K. Shibatomi, T. Shirai*
    Chem. Asian J.<\/em> 2023<\/strong>, 18<\/em>, e202300533.\u00a0 DOI:     10.1002\/asia.202300533<\/a><\/li>\n\n\n\n
  17. Zinc\u2010Mediated Diastereoselective Annulation of Cyclopropanols with Alkylidenemalononitriles via Enolized Homoenolate<\/strong>
    K. Tsukiji, T. Hayakawa, K. Kanemoto, N. Yoshikai*
    Asian J. Org. Chem.<\/em> 2023<\/strong>, 12<\/em>, e202300114.  DOI:     10.1002\/ajoc.202300114<\/a><\/li>\n\n\n\n
  18. N<\/em>-(Morpholine-4-dithio)phthalimide: A Shelf-Stable, Bilateral Platform Molecule Enabling Access to Diverse Unsymmetrical Disulfides<\/strong>
    H. Asanuma, K. Kanemoto,* T. Watanabe, S.-i. Fukuzawa*
    Angew. Chem., Int. Ed.<\/em> 2023<\/strong>, 62<\/em>, e202219156. Angew. Chem.<\/em> 2023<\/strong>, 135<\/em>, e202219156.  DOI:     10.1002\/anie.202219156<\/a>
    \u3010Highlighted in Synfacts<\/em>, 2023<\/strong>, 19<\/em>, 0617.\u3011
    \"\"<\/li>\n\n\n\n
  19. Chiral Silver Complex-Catalyzed Asymmetric Conjugate Addition of 1\u2011Pyrroline-5-Carbonitrile to \u03b1\u2011Enones<\/strong>
    H. Araki, S. Furuya, K. Kanemoto, S.-i. Fukuzawa*
    J. Org. Chem.<\/em> 2023<\/strong>, 88<\/em>, 924.  DOI:     10.1021\/acs.joc.2c02315<\/a><\/li>\n\n\n\n
  20. Diastereoselective Conversion of Cyclopropanols to Cyclopentane-1,3-diols via Aldol Dimerization of Zinc Homoenolates<\/strong>
    K. Tsukiji, Y. Sekiguchi, K. Kanemoto, N. Yoshikai*
    Chem. Lett.<\/em> 2022<\/strong>, 51<\/em>, 1012.  DOI:     10.1246\/cl.220311<\/a><\/li>\n\n\n\n
  21. exo\u02b9<\/em>-Selective Construction of Dispiropyrrolidines by the Silver-catalyzed Asymmetric [3+2] Cycloaddition of Imino Esters with 4-Benzylidene-2,3-dioxopyrrolidines<\/strong>
    S. Furuya, K. Kanemoto,* S.-i. Fukuzawa*
    Chem. Asian J.<\/em> 2022<\/strong>, 17<\/em>, e202200239.  DOI:     10.1002\/asia.202200239<\/a>
    \"\"<\/li>\n\n\n\n
  22. Synthesis and Evaluation of Novel Planar-Chiral Monophosphine Ligands Bearing Ferrocene-Triazole Backbones<\/strong>
    S. Sakai, K. Kanemoto,* S.-i. Fukuzawa*
    Eur. J. Inorg. Chem. <\/em>2022<\/strong>, e202100967.  DOI:     10.1002\/ejic.202100967<\/a>
    \"\"<\/li>\n\n\n\n
  23. Cationic Iridium-Catalyzed Asymmetric Decarbonylative Aryl Addition of Aromatic Aldehydes to Bicyclic Alkenes<\/strong>
    R. Nonami, Y. Morimoto, K. Kanemoto, Y. Yamamoto, T. Shirai*
    Chem. Eur. J.<\/em> 2022<\/strong>, 28<\/em>, e202200317.  DOI:     10.1002\/chem.202200317<\/a>
    \u3010Selected as supplementary cover\u3011\u3010Selected as hot paper\u3011<\/li>\n\n\n\n
  24. Synthesis and properties of 5,5\u2019-diethynyl indigos and their polymers using Glaser coupling reaction<\/strong>
    S. Kenmochi, K. Kanemoto, T. Ikeda, S.-i. Fukuzawa
    Fac. Sci. Eng. Chuo Univ.<\/em> 2022<\/strong>, 27, 35.<\/li>\n\n\n\n
  25. Trifluoroacetic Acid-Mediated Desulfurilative Sulfonylation of Activated Olefins Using Potassium p<\/em>-Toluenethiosulfonate<\/strong>
    T. Watanebe, K. Kanemoto,* S.-i. Fukuzawa
    Bull. Fac. Sci. Eng., Chuo Univ.<\/em> 2022<\/strong>, 27<\/em>, 15.<\/li>\n\n\n\n
  26. Silver\/ThioClickFerrophos-Catalyzed 1,3-Dipolar Cycloaddition and Tandem Addition-Elimination Reaction of Morita\u2013Baylis\u2013Hillman Adducts<\/strong>
    Y. Suzuki, K. Kanemoto,* A. Inoue, K. Imae, S.-i. Fukuzawa*
    J. Org. Chem.<\/em>2021<\/strong>,86<\/em>, 14586.  DOI:     10.1021\/acs.joc.1c01440<\/a>
    \"\"<\/li>\n\n\n\n
  27. Copper-Catalyzed Single C\u2013H Amination of 8-Aminoquinoline-Directed Ferrocenes<\/strong>
    K. Kanemoto,* N. Horikawa, S. Hoshino, Y. Tokoro, S.-i. Fukuzawa*
    Org. Lett<\/em>. 2021<\/strong>, 23<\/em>, 4966.  DOI:     10.1021\/acs.orglett.1c01294<\/a>
    \u3010Selected as supplementary cover\u3011
    \"\"<\/li>\n\n\n\n
  28. Palladium-Catalyzed Sulfinylation of Aryl- and Alkenylborons with Sulfinate Esters<\/strong>
    M. Suzuki, K. Kanemoto, Y. Nakamura, T. Hosoya, S. Yoshida*
    Org. Lett<\/em>. 2021<\/strong>, 23<\/em>, 3793.  DOI:     10.1021\/acs.orglett.1c01292<\/a><\/li>\n\n\n\n
  29. Acid-Mediated Sulfonylthiolation of Arenes via Selective Activation of SS<\/em>-Morpholino Dithiosulfonate<\/strong>
    K. Kanemoto,* K. Furuhashi, Y. Morita, T. Komatsu, S.-i. Fukuzawa*
    Org. Lett<\/em>. 2021<\/strong>, 23<\/em>, 1582.  DOI:     10.1021\/acs.orglett.0c04289<\/a>
    \u3010    Highlighted in Organic Chemistry Portal<\/a>\u3011\u3010Selected as supplementary cover\u3011
    \"\"<\/li>\n\n\n\n
  30. Copper-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Imino Esters to Unsaturated Sultones<\/strong>
    S. Furuya, K. Kanemoto,* S.-i. Fukuzawa*
    J. Org. Chem. <\/em>2020<\/strong>, 85<\/em>, 8142.  DOI:     10.1021\/acs.joc.0c01023<\/a>
    \u3010Highlighted in Synfacts<\/em>, 2020<\/strong>, 10<\/em>,1118.\u3011
    \"\"<\/li>\n\n\n\n
  31. Cationic Iridium\/Chiral Bisphosphine\u2010Catalyzed Enantioselective Hydroacylation of Ketones<\/strong>
    T. Shirai,* T. Iwasaki, K. Kanemoto, Y. Yamamoto
    Chem. Asian J.<\/em> 2020<\/strong>, 15<\/em>, 1858.  DOI:     10.1002\/asia.202000386<\/a><\/li>\n\n\n\n
  32. Functionalization of a Single C\u2013F Bond of Trifluoromethylarenes Assisted by an ortho<\/em>-Silyl Group Using a Trityl-Based All-in-One Reagent with Ytterbium Triflate Catalyst<\/strong>
    Y. Kim, K. Kanemoto, K. Shimomori, T. Hosoya, S. Yoshida*
    Chem. Eur. J.<\/em> 2020<\/strong>, 26<\/em>, 6136.  DOI:     10.1002\/chem.202001315<\/a><\/li>\n\n\n\n
  33. Synthesis of Phenoxathiins and Phenothiazines by Aryne Reactions with Thiosulfonates<\/strong>
    K. Kanemoto, Y. Sakata, T. Hosoya, S. Yoshida*
    Chem. Lett. <\/em>2020<\/strong>, 49<\/em>, 593.  DOI:     10.1246\/cl.200132<\/a>
    \"\"<\/li>\n\n\n\n
  34. Synthesis of Alkynyl Sulfides by Copper-Catalyzed Thiolation of Terminal Alkynes Using Thiosulfonates<\/strong>
    K. Kanemoto, S. Yoshida*, T. Hosoya*
    Org. Lett.<\/em> 2019<\/strong>, 21<\/em>, 3172.  DOI:     10.1021\/acs.orglett.9b00875<\/a>
    \u3010    Press Release<\/a>\u3011\u3010Most downloaded article of Org. Lett.<\/em> in April 2019\u3011
    \u3010    Highlighted in Organic Chemistry Portal<\/a>\u3011
    \"\"<\/li>\n\n\n\n
  35. Copper-Catalyzed Regio- and Diastereoselective 1,3-Dipolar Cycloaddition Reactions of Glycine Imino Esters with 1-Propene-1,3-sultone<\/strong>
    S. Furuya, S. Kato, K. Kanemoto, S.-i. Fukuzawa*
    Eur. J. Org. Chem.<\/em> 2019<\/strong>, 4561.  DOI:     10.1002\/ejoc.201900738<\/a><\/li>\n\n\n\n
  36. Facile Synthesis of Diverse o<\/em>-Iodoaryl Triflates from o<\/em>-Silylaryl Triflates by Aluminum-mediated Desilyliodination<\/strong>
    S. Yoshida*, Y. Hazama, K. Kanemoto, Y. Nakamura, T. Hosoya*
    Chem. Lett.<\/em> 2019<\/strong>, 48<\/em>, 742.  DOI:     10.1246\/cl.190223<\/a><\/li>\n\n\n\n
  37. Modular Synthesis of Unsymmetrical Doubly-ring-fused Benzene Derivatives Based on a Sequential Ring Construction Strategy Using Oxadiazinones as a Platform Molecule<\/strong>
    T. Meguro, S. Chen, K. Kanemoto, S. Yoshida *, T. Hosoya*
    Chem. Lett.<\/em> 2019<\/strong>, 48, 582.  DOI:     10.1246\/cl.190118<\/a><\/li>\n\n\n\n
  38. Modified Conditions for Copper-catalyzed ipso<\/em>-Thiolation of Arylboronic Acid Esters with Thiosulfonates<\/strong>
    K. Kanemoto, S. Yoshida*, T. Hosoya*
    Chem. Lett<\/em>. 2018<\/strong>, 47<\/em>, 85.  DOI:     10.1246\/cl.170907<\/a>
    \"\"<\/li>\n\n\n\n
  39. Rhodium-catalyzed odorless synthesis of diaryl sulfides from borylarenes and S<\/em>-aryl thiosulfonates<\/strong>
    K. Kanemoto, Y. Sugimura, S. Shimizu, S. Yoshida*, T. Hosoya*
    Chem. Commun.<\/em> 2017<\/strong>, 53<\/em>, 10640.  DOI:     10.1039\/C7CC05868C<\/a>
    \"\"<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

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