Published Papers & Misc - HOSOYA Takamitsu

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  1. Nakamura Y, Ozawa S, Yoshida S, Hosoya T. Facile Synthesis of Diverse 2,6-Disubstituted Arylsilanes via Silylamination and Silylsulfanylation of Aryne Intermediates Generated from o-Iodoaryl Triflates. Chem Lett. 2019.11; 48 (11): 1296-1299. ( DOI )

  2. Uchida K, Minami Y, Yoshida S, Hosoya T. Synthesis of Diverse γ-Aryl-β-ketoesters via Aryne Intermediates Generated by C-C Bond Cleavage. Org Lett. 2019.11; 21 (22): 9019-9023. ( PubMed, DOI )

  3. Yoshida S, Goto S, Nishiyama Y, Hazama Y, Kondo M, Matsushita T, Hosoya T. Effect of Resonance on the Clickability of Alkenyl Azides in the Strain-promoted Cycloaddition with Dibenzo-fused Cyclooctynes. Chem Lett. 2019.09; 48 (9): 1038-1041. ( DOI )

  4. Yoshida S, Hazama Y, Kanemoto K, Nakamura Y, Hosoya T. Facile Synthesis of Diverse o-Iodoaryl Triflates from o-Silylaryl Triflates by Aluminum-mediated Desilyliodination. Chem Lett. 2019.07; 48 (7): 742-745. ( DOI )

  5. Nakamura Y, Miyata Y, Uchida K, Yoshida S, Hosoya T. 3-Thioaryne Intermediates for the Synthesis of Diverse Thioarenes. Org Lett. 2019.07; 21 (13): 5252-5258. ( PubMed, DOI )

  6. Uetake Y, Isoda M, Niwa T, Hosoya T. Synthesis of (2,2-Diborylvinyl)arenes by Rhodium-Catalyzed Desulfanylative gem-Diborylation of 2-Arylvinyl Sulfides. Org Lett. 2019.07; 21 (13): 4933-4938. ( PubMed, DOI )

  7. Nishiyama Y, Misawa Y, Hazama Y, Oya K, Yoshida S, Hosoya T. Synthesis of Diverse 3-Azido-5-(azidomethyl)benzene Derivatives via Formal C–H Azidation and Functional Group-Selective Transformations. Heterocycles. 2019.06; 99 (2): 1053-1072. ( DOI )

  8. Yoshida S, Hosoya T. Target Identification of Bioactive Compounds by Photoaffinity Labeling Using Diazido Probes. Cutting-Edge Organic Synthesis and Chemical Biology of Bioactive Molecules – The Shape of Organic Synthesis to Come. 2019.06; 335-355. ( DOI )

  9. Meguro T, Chen S, Kanemoto K, Yoshida S, Hosoya T. Modular Synthesis of Unsymmetrical Doubly-ring-fused Benzene Derivatives Based on a Sequential Ring Construction Strategy Using Oxadiazinones as a Platform Molecule. Chem Lett. 2019.06; 48 (6): 582-585. ( DOI )

  10. Watanabe K, Tsuda J, Ochiai H, Niwa T, Hosoya T. Divergent Synthesis of Photoaffinity Probe Candidates by Click Reactions of Azido-Substituted Aryltrifluoromethyldiazirines. Heterocycles. 2019.06; 99 (2): 1366-1387. ( DOI )

  11. Kanemoto K, Yoshida S, Hosoya T. Synthesis of Alkynyl Sulfides by Copper-Catalyzed Thiolation of Terminal Alkynes Using Thiosulfonates. Org Lett. 2019.04; 21 (9): 3172-3177. ( PubMed, DOI )

  12. Yoshida S, Kuribara T, Ito H, Meguro T, Nishiyama Y, Karaki F, Hatakeyama Y, Koike Y, Kii I, Hosoya T. A facile preparation of functional cycloalkynes via an azide-to-cycloalkyne switching approach. Chem Commun. 2019.03; 55 (24): 3556-3559. ( PubMed, DOI )

  13. Toyoda Y, Morimoto K, Suno R, Horita S, Yamashita K Hirata K, Sekiguchi Y, Yasuda S, Shiroishi M, Shimizu T, Urushibata Y, Kajiwara Y, Inazumi T, Hotta Y, Asada H, Nakane T, Shiimura Y, Nakagita T, Tsuge K, Yoshida S, Kuribara T, Hosoya T, Sugimoto Y, Nomura N, Sato M, Hirokawa T, Kinoshita M, Murata T, Takayama K, Yamamoto M, Narumiya S, Iwata S, Kobayashi T. Ligand binding to human prostaglandin E receptor EP4 at the lipid-bilayer interface. Nat Chem Biol. 2019.01; 15 (1): 18-26. ( PubMed, DOI )

  14. Zhang Z, Niwa T, Watanabe Y, Hosoya T. Palladium(II)-mediated rapid 11C-cyanation of (hetero)arylborons. Org Biomol Chem. 2018.11; 16 (41): 7711-7716. ( PubMed, DOI )

  15. Takahashi K, Hosoya T, Onoe K, Takashima T, Tanaka M, Ishii A, Nakatomi Y, Tazawa S, Takahashi K, Doi H, Wada Y, Watanabe Y. Association between aromatase in human brains and personality traits. Sci Rep. 2018.11; 8 (1): 16841. ( PubMed, DOI )

  16. Yoshida S, Tanaka J, Nishiyama Y, Hazama Y, Matsushita T, Hosoya T. Further enhancement of the clickability of doubly sterically-hindered aryl azides by para-amino substitution. Chem Commun. 2018.11; 54 (96): 13499-13502. ( PubMed, DOI )

  17. Matsuzawa T, Yoshida S, Hosoya T. Recent advances in reactions between arynes and organosulfur compounds. Tetrahedron Lett. 2018.10; 59 (48): 4197-4208 . ( DOI )

  18. Sumida Y, Harada R, Sumida T, Hashizume D, Hosoya T. Hydrosilyl Group-directed Iridium-catalyzed peri-Selective C–H Borylation of Ring-fused (Hetero)Arenes. Chem Lett. 2018.10; 47 (10): 1251-1254. ( DOI )

  19. Nishiyama Y, Kamada S, Yoshida S, Hosoya T. Generation of Arynes by Selective Cleavage of a Carbon–Phosphorus Bond of o-(Diarylphosphinyl)aryl Triflates Using a Grignard Reagent. Chem Lett. 2018.09; 47 (9): 1216-1219. ( DOI )

  20. Inouye S, Tomabechi Y, Hosoya T, Sekine S, Shirouzu M. Slow luminescence kinetics of semi-synthetic aequorin: expression, purification and structure determination of cf3-aequorin. J Biochem. 2018.09; 164 (3): 247-255. ( PubMed, DOI )

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