Yuji Sumii

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2012-2013 California Institute of Technology, Pasadena, CA 
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"Yuji Sumii"
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Goldstein EL, Takada H, Sumii Y, et al. (2022) Synthesis of enantioenriched 2,2-disubstituted pyrrolidines via sequential asymmetric allylic alkylation and ring contraction. Tetrahedron. 123
Iwaki K, Tanagawa K, Mori S, et al. (2022) Regioselective Synthesis of Pyridine-SF-Methyl Ketones via Hydration of Pyridine-SF-Alkynes. Organic Letters. 24: 3347-3352
Sumii Y, Kotoku N, Han C, et al. (2020) 3-(Phenethylamino)demethyl(oxy)aaptamine as an anti-dormant mycobacterial substance: Isolation, evaluation and total synthesis. Tetrahedron Letters. 61
Zhou J, Jiang B, Guo M, et al. (2020) Aryl gem-Difluorovinyl Pinacolboronates: Synthesis and Utility for Suzuki-Miyaura Coupling Reaction Chemistry Letters
Hirano K, Yoshioka K, Umezu K, et al. (2020) One-step Synthesis of 2-Hydroxy-2-(trifluoromethyl)malonates by Trifluoromethylation of 2-Oxomalonates with Ruppert-Prakash Reagent Chemistry Letters. 49: 330-333
Niina K, Tanagawa K, Sumii Y, et al. (2020) Pyridine tetrafluoro-λ6-sulfanyl chlorides: spontaneous addition to alkynes and alkenes in the presence or absence of photo-irradiation Organic Chemistry Frontiers. 7: 1276-1282
Sumii Y, Sasaki K, Tsuzuki S, et al. (2019) Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design. Molecules (Basel, Switzerland). 24
Kawachi T, Tanaka S, Fukuda A, et al. (2019) Target Identification of the Marine Natural Products Dictyoceratin-A and -C as Selective Growth Inhibitors in Cancer Cells Adapted to Hypoxic Environments. Marine Drugs. 17
Gondo S, Matsubara O, Chachignon H, et al. (2019) Asymmetric Electrophilic Difluoromethylthiolation of Indanone-Based β-Keto Esters Using Difluoromethanesulfonyl Hypervalent Iodonium Ylides. Molecules (Basel, Switzerland). 24
Sumii Y, Hibino H, Saidalimu I, et al. (2018) Design and synthesis of galactose-conjugated fluorinated and non-fluorinated proline oligomers: towards antifreeze molecules. Chemical Communications (Cambridge, England). 54: 9749-9752
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