Publication

Dr. Yuto Sumida

Original publications

  1. Organic Photoredox-Catalyzed Silyl Radical Generation from Silylboronate
    1. Takemura, N.; Sumida, Y.; Ohmiya, H.
    2. ACS Catal. 2022, 12, 7804–7810.
    3. 10.1021/acscatal.2c01964
  2. Direct Photoexcitable Iodomethylborate Enabling Cyclopropanation of Reactive Alkenes
    1. Nakamura, R.; Sumida, Y.; Ohmiya, H.
    2. Bull. Chem. Soc. Jpn. 2022 , 95, 1001–1005.
    3. DOI: 10.1246/bcsj.20220112
  3. Direct Photoexcitation of Borate Enabling Minisci Reaction
    1. Kemmochi, M.; Miyamoto, Y.; Sumida, Y.; Ohmiya, H.
    2. Asian. J. Org. Chem. 2021, 11, e2021006 (AsianJOCs 10th Anniversary Special Collection).
    3. DOI: 10.1002/ajoc.202100640
  4. Light-Driven N-Heterocyclic Carbene Catalysis Using Alkylborates
    1. Sato, Y.; Goto, Y.; Nakamura, K.; Miyamoto, Y.; Sumida, Y.; Ohmiya, H.
    2. ACS Catal. 2021, 11, 12886–12892.
    3. DOI: 10.1021/acscatal.1c04153
  5. Generation of Functionalized Alkyl Radicals via the Direct Photo-Excitation of PDP-Based Borates
    1. Miyamoto, Y.; Sumida, Y.; Ohmiya, H.
    2. Org. Lett. 2021, 23, 5865–5870.
    3. DOI: 10.1021/acs.orglett.1c01996
  6. Chiral deaza-coelenterazine analogs for probing a substrate-binding site in the Ca2+-binding photoprotein aequorin
    1. Inouye, S.; Sumida, Y.; Tomabechi, Y.; Taguchi, J.; Shirouzu, M.; Hosoya, T.
    2. PLOS ONE 2021, 16(6): e0251743.
    3. DOI: 10.1371/journal.pone.0251743 
  7. Fluorescent-oxaboroles: Synthesis and Optical Property by Sugar Recognition
    1. Nakano, M.; Nakamura, R.; Sumida, Y.; Nagao, K.; Furuyama, T.; Inagaki, F.; Ohmiya, H.
    2. Chem. Pharm. Bull. 2021, 69, 526–528 (Featured Article).
    3. DOI: 10.1248/cpb.c21-00179
  8. Direct Excitation Strategy for Radical Generation in Organic Synthesis
    1. Sumida, Y.; Ohmiya, H.
    2. Chem. Soc. Rev. 2021, 50, 6320–6332.
    3. DOI: 10.1039/d1cs00262g
  9. Synthesis of Dibenzofurans by Cu-Catalyzed Deborylative Ring Contraction of Dibenzoxaborins
    1. Sumida, Y.; Harada, Y.; Sumida, T.; Johmoto, K.; Uekusa, H.; Hosoya, T.
    2. Org. Lett., 2020, 22, 6687–6691.
    3. DOI: 10.1021/acs.orglett.0c02584
  10. Boracene-Based Alkylborate Enabling Ni/Ir Hybrid Catalysis
    1. Sato, Y.; Miyamoto, Y.; Sumida, Y.; Hosoya, T.; Ohmiya, H.
    2. Org. Biomol. Chem. 2020, 18, 6598–6601.
    3. DOI: 10.1039/D0OB01610A
  11. Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate
    1. Sato, Y.; Nakamura, K.; Sumida, Y.; Hashizume, D.; Hosoya, T.; Ohmiya, H.
    2. J. Am. Chem. Soc. 2020, 142, 9938–9943.
    3. DOI: 10.1021/jacs.0c04456
  12. Aliphatic Oxaboroles Enabling Remarkable Recognition of Diol
    1. Arakawa, N.; Nagao, K.; Murakami, R.; Sumida, Y.; Arakawa, H.; Inagaki, F.; Ohmiya, H.
    2. Bull. Chem. Soc. Jpn. 2020​, 93, 576–580.
    3. DOI: 10.1246/bcsj.20200007
  13. Hydrosilyl Group-Directed Iridium-Catalyzed peri-Selective C–H Borylation of Ring-Fused (Hetero)Arenes
    1. Sumida, Y.; Harada, R.; Sumida, T.; Hashizume, D.; Hosoya, T.
    2. Chem. Lett., 2018, 47, 1251–1254.
    3. DOI: 10.1246/cl.180594
  14. A study on an unusual SN2 mechanism in the methylation of benzyne through nickel-complexation
    1. Hatakeyama, M.; Sakamoto, Y.; Ogata, K.; Sumida, Y.; Sumida, T.; Hosoya, T.; Nakamura, S.
    2. Phys. Chem. Chem. Phys. 2017, 19, 26926–26933.
    3. DOI: 10.1039/c7cp04739h
  15. Prenatal neurogenesis induction therapy normalizes brain structure and function in Down syndrome mice
    1. Nakano-Kobayashi, A.; Awaya, T.; Kii, I.; Sumida, T.; Okuno, Y.; Yoshida, S.; Sumida, T.; Inoue, H.; Hosoya, T.; Hagiwara, M.
    2. Proc. Natl. Acad. Sci. USA. 2017, 114, 10268–10273.
    3. DOI: 10.1073/pnas.1704143114
  16. Nickel-Catalyzed Reductive Cross-Coupling of Aryl Triflates and Nonaflates with Alkyl Iodides
    1. Sumida, Y.; Sumida, T.; Hosoya, T.
    2. Synthesis 2017, 49, 3590–3601.
    3. DOI: 10.1055/s-0036-1588464
  17. Preparation of Aryne−Nickel Complexes from ortho-Borylaryl Triflates
    1. Sumida, Y.; Sumida, T.; Hashizume, D.; Hosoya, T.
    2. Org. Lett. 2016, 18, 5600–5603.
    3. DOI: 10.1021/acs.orglett.6b02831
  18. Selective inhibition of the kinase DYRK1A by targeting its folding process
    1. Kii, I.; Sumida, Y.; Goto, T.; Sonamoto, R.; Okuno, Y.; Yoshida, S.; Kato-Sumida, T.; Koike, Y.; Abe, M.; Nonaka, Y.; Ikura, T.; Ito, N.;Shibuya, H.; Hosoya, T.; Hagiwara, M.
    2. Nat. Commun. 2016, 7, 11391.
    3. DOI: 10.1038/ncomms11391
  19. Concise Synthesis of v-Coelenterazines
    1. Ohta, Y.; Yasuda, S.; Yokogawa, Y.; Kurokawa, K.; Hosoya, T.; Iimori, R.; Yoshida, S.; Sumida, Y.; Sahara-Miura, Y.; Sato, J.-i.; Inouye, S.
    2. Org. Lett. 2015, 17, 3888–3891.
    3. DOI: 10.1021/acs.orglett.5b01872
  20. Identification of a DYRK1A Inhibitor that Induces Degradation of the Target Kinase using Co-chaperone CDC37 fused with Luciferase nanoKAZ
    1. Sonamoto, R.; Kii, I.; Koike, Y.; Sumida, Y.; Kato-Sumida, T.; Hosoya, T.; Hagiwara, M.
    2. Sci. Rep. 2015, 5, 12728.
    3. DOI: 10.1038/srep12728
  21. Design and synthesis of a potent inhibitor of class 1 DYRK kinases as a suppressor of adipogenesisMasaki,S.;Kii, I.; Sumida, Y.; Kato-Sumida, T.;Ogawa, Y.; Ito, N.; Nakamura, M.; Sonamoto, R.; Kataoka, N.; Hosoya, T. Hagiwara, M.
    1. Bioorg. Med. Chem. 2015, 23, 4434–4441.
    2. DOI: 10.1016/j.bmc.2015.06.018
  22. An Alternative Method for Generating Arynes from ortho-Silylaryl Triflates: Activation by Cesium Carbonate in the Presence of a Crown Ether
    1. Yoshida, S.; Hazama, Y.; Sumida, Y.;Yano, T.; Hosoya, T.
    2. Molecules 2015, 20, 10131–10140.
    3. DOI: 10.3390/molecules200610131
  23. Boron-Selective Biaryl Coupling Approach to Versatile Dibenzoxaborins and Application to Concise Synthesis of Defucogilvocarcin M
    1. Sumida, Y.; Harada, R.; Kato-Sumida, T.;Johmoto, K.; Uekusa, H.; Hosoya, T.
    2. Org. Lett. 2014, 16, 6240–6243.
    3. DOI: 10.1021/ol5031734
  24. Generation of Arynes via Ate Complexes of Arylboronic Esters with an ortho-Leaving Group.
    1. Sumida, Y.; Kato, T.; Hosoya, T.
    2. Org. Lett. 2013, 15, 2806–2809.
    3. DOI: 10.1021/ol401140d
  25. Palladium-Catalyzed Regio- and Stereoselective Hydrosilylation of Electron-Deficient Alkynes.
    1. Sumida, Y.; Kato, T.; Yoshida, S.; Hosoya, T.
    2. Org. Lett. 2012, 14, 1552–1555.
    3. DOI: 10.1021/ol300279c
  26. Primer Preactivation of Peptidoglycan Polymerases.
    1. Wang, T-S. A.; Lupoli, T. J.; Sumida, Y.; Tsukamoto, H.; Wu, Y.; Rebets, Y.; Kahne, D. E.; Walker, S.
    2. J. Am. Chem. Soc. 2011, 133, 8528–8530.
    3. DOI: 10.1021/ja2028712
  27. Nickel-Catalyzed Arylative Ring-Opening of 3-Methylenecycloalkane-1,1- dicarboxylate.
    1. Sumida, Y.; Yorimitsu, H.; Oshima, K.
    2. Org. Lett. 2010,12, 2254–2257.
    3. DOI: 10.1021/ol100599c
  28. Radical Addition of Polyhaloalkanes to 2-Ethynyl-4,4,5,5-tetramethyl-1,3-2-dioxaboronate.
    1. Wada, T.; Sumida, Y.; Kondoh, A.; Yorimitsu, H.; Oshima, K.
    2. Bull. Chem. Soc. Jpn. 2009, 82, 1433–1435.
    3. DOI:10.1246/bcsj.82.1433
  29. Palladium-Catalyzed Preparation of Silyl Enolates from α,β-Unsaturated Ketones or Cyclopropyl Ketones with Hydrosilanes.
    1. Sumida, Y.; Yorimitsu, H.; Oshima, K.
    2. J. Org. Chem. 2009, 74, 7986–7989.
    3. DOI: 10.1021/jo901513v
  30. Nickel-Catalyzed Borylation of Aryl Cyclopropyl Ketones with Bis(pinacolato)diboron to Synthesize 4-Oxoalkylboronates.
    1. Sumida, Y.; Yorimitsu, H.; Oshima, K.
    2. J. Org. Chem. 2009, 74, 3196–3198.
    3. DOI: 10.1021/jo900071m
  31. Nickel-Catalyzed BorylativeRing-Opening Reaction ofVinylcyclopropanes with Bis(pinacolato)diboron Yielding Allylic Boronates.
    1. Sumida, Y.; Yorimitsu, H.; Oshima, K.
    2. Org. Lett. 2008,10, 4677–4679.
    3. DOI: 10.1021/ol801982d
  32. Nickel-Catalyzed Allylation of Allyl Carbonates with Homoallyl Alcohols via Retro-Allylation Providing 1,5-Hexadienes.
    1. Sumida, Y.; Hayashi, S.; Hirano, K.; Yorimitsu, H.; Oshima, K.
    2. Org. Lett. 2008,10, 1629–1632.
    3. DOI: 10.1021/ol800335v
  33. Rhodium-Catalyzed Allylation of Aldehydes with Homoallyl Alcohols via Retroallylation and Isomerization to Saturated Ketones with Conventional or Microwave Heating.
    1. Sumida, Y.;Takada, Y.; Hayashi, S.; Hirano, K.;Yorimitsu, H.; Oshima, K.
    2. Chem. Asian J. 2008,1, 119–125.
    3. DOI: 10.1002/asia.200700255
  34. Discrepancy of the spectral data between adunctin E and the synthetic one
    1. Yamashita, M.; Yadav, N. D.; Sumida, Y.;Kawasaki, I.; Kurume, A.; Ohta, S.
    2. Tetrahedron Lett. 2007, 48,5619–5622.
    3. DOI: 10.1016/j.tetlet.2007.06.050

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