Acknowledgements
(Research results contributed by CIF -Part 1-)



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32 (MS, FT-IR; Dr. K. Oyama).
    Tomoya Kanda,Asuka Naraoka,Hiroshi Naka
    J. Am. Chem. Soc. 2019, 141, 825－830      DOI: 10.1021/jacs.8b12877.


31 (Elemental analysis; Dr. K. Oyama).
    Haruki Inada, Masatoshi Shibuya,Yoshihiko Yamamoto
    Org. Lett. 2019, 21, 709－713      DOI: 10.1021/acs.orglett.8b03910.


30 (Chromatography; Dr. K. Oyama).
    Koichi Mimura, Riku Okada, Tamihito Nishida
    J. Chromatogr. A 2018, 1566, 118-123.      DOI: 10.1016/j.chroma.2018.06.051


29 (Elemental analysis; Dr. K. Oyama).
    Shin-ichiro Kawano, Tomoaki Fukushima, and Kentaro Tanaka
    Angew. Chem. Int. Ed. 2018, 57, 14827-14831.      DOI: 10.1002/anie.201809167


28 (MS; Dr. K. Oyama).
    Taizo Mori, Hiroyuki Tanaka, Amit Dalui, Nobuhiko Mitoma, Kengo Suzuki, Mutsuyoshi Matsumoto, Nikhil Aggarwal, Archita Patnaik, Somobrata Acharya, Lok Kumar Shrestha, Hirotoshi Sakamoto, Kenichiro Itami, and Katsuhiko Ariga
    Angew. Chem. Int. Ed. 2018, 57, 6979-9683.      DOI: 10.1002/anie.201803859


27 (MS; Dr. K. Oyama).
    Jianhua Qi, Lihong Cheng, Yujuan Sun, Yushi Hirata, Naoki Ushida, Zhonghua Ma, Hiroyuki Osada, Toshio Nishikawa, Lan Xiang
    Angew. Chem. Int. Ed. 2018, 57, 8100-8104.      DOI: 10.1002/anie.201803329


26 (Elemental analysis; Dr. K. Oyama).
    H. Hattori, S. Yokoshima, T. Fukuyama
    Angew. Chem. Int. Ed. 2017, 56, 6980-6983.      DOI: 10.1002/anie.201702204


25 (MS; Dr. K. Oyama).
    M. Naruto, S. Agrawal, K. Toda, S. Saito
    Sci, Rep. 2017, 7, 3425.      DOI: 10.1038/s41598-017-03436-y


24 (MS; Dr. K. Oyama).
    T. Miura, M. Naruto, K. Toda, T. Shimomura, S. Saito
    Sci, Rep. 2017, 7, 1586.      DOI: 10.1038/s41598-017-01645-z


23 (FT-IR, MS; Dr. K. Oyama).
    Qingcai Chen,Fumikazu Ikemori,Yuua Nakamura,Petr Vodicka,Kimitaka Kawamura,Michihiro Mochida
    AEnviron. Sci. Technol. 2017, 51, 8293-8303      DOI: 10.1021/acs.est.7b01630


22 (CD; Dr. K. Oyama).
    T. Tomura, S. Nagashima, S. Yamazaki, T. Iizuka, R. Fudou, M. Ojika
    Mar. Drugs 2017, 15, 109.

21 (Elemental analysis; Dr. K. Oyama).
    N. Mihara, Y. Yamada, H. Takaya, Y. Kitagawa, S. Aoyama, K. Igawa, K. Tomooka, K. Tanaka
    Chem. Eur. J. 2017, 23, 7508-7514.


20 (fluorescence, UV-vis, FT-IR; Dr. K. Oyama).
    Qingcai Chen,Fumikazu Ikemori,Yuua Nakamura,Petr Vodicka,Kimitaka Kawamura,Michihiro Mochida
    Environ. Sci. Technol. 2016, 50, 10859－10868      DOI: 10.1021/acs.est.6b02541


19 (MS, Elemental analysis; Dr. K. Oyama).
    S. Wakabayashi, Y. Hori, S. Komeda, Y. Shimizu, Y. Ohki, M. Horiuchi,T. Itoh, Y. Sugihara, K. Tatsumi
    J. Org. Chem. 2016, 81, 2399-2404.


18 (MS; Dr. K. Oyama).
    J.-I. Ito, S. Ubukata, S. Muraoka, H. Nishiyama
    Chem. Eur. J. 2016, 22, 16801-16804.


17 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, T. Kato, K. Tanaka
    Chem. Eur. J. 2016, 22, 12371-12380.


16 (Elemental analysis; Dr. K. Oyama).
    A. Alexandrov, T. Asada, A. Buonaura, L. Consiglio, N. D窶僊mbrosio,
    G. De Lellis, A. Di Crescenzo, N. Di Marco, M.L. Di Vacri, S. Furuya, G. Galati,
    V. Gentile, T. Katsuragawa, M. Laubenstein, A. Lauria, P.F. Loverre, S. Machii,
    P. Monacelli, M.C. Montesi, T. Naka, F. Pupilli, G. Rosa, O. Sato,
    P. Strolin, V. Tioukov, A. Umemoto, M. Yoshimoto
    Astroparticle Physics 2016, 80, 16-21.


15 (MS; Dr. K. Oyama).
    A. Matsuoka, T. Isogawa, Y. Morioka, B. R. Knappett, A. E. H. Wheatley, S. Saito, H. Naka
     RSC Adv., 2015, 5, 12152-12160.      DOI: 10.1039/C4RA15682J


14 (Elemental analysis; Dr. K. Oyama).
    S. Kawano, Y. Ishida, K. Tanaka
    J. Am. Chem. Soc. 2015, 137, 2295-2302.      DOI: 10.1021/ja510585u


13 (MS; Dr. K. Oyama).
    Y. Takada, S. W. Foo, Y. Yamazaki, S. Saito
     RSC Adv., 2014, 4, 50851-50857.      DOI: 10.1039/C4RA09609F


12 (MS; Dr. K. Oyama).
    H. Shirouzu, H. Morita, M. Tsukamoto
     Tetrahedron 2014, 70, 3635-3639.      DOI:10.1016/j.tet.2014.03.013


11 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, S. Matsumoto, K. Yamada, T. Nishino, N. Mihara, K. Sugimoto, K. Tanaka
    Chem. Lett. 2014, 43, 1377-1379.      DOI: 10.1246/cl.140392


10 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, T. Kubota, M. Nishino, K. Tanaka
    J. Am. Chem. Soc. 2014, 136, 6505-6509.      DOI: 10.1021/ja502898t


9 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, N. Mihara, S. Shibano, K. Sugimoto, K. Tanaka
    J. Am. Chem. Soc. 2013, 135, 11505-11508.      DOI: 10.1021/ja405963t

8 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, N. Mihara, S. Shibano, K. Sugimoto, K. Tanaka
    Dalton Trans., 2013, 42, 15873-15876.      DOI: 10.1039/C3DT51043C


7 (MS; Dr. K. Oyama).
    S. Wakabayashi, M. Uchida, R. Tanaka, Y. Habata, M. Shimizu,
     Asian J. Org. Chem. 2013, 2, 786 -791.      DOI: 10.1002/ajoc.201300131


6 (MS; Dr. K. Oyama).
    Y. Yamamoto, S. Yamada, H. Nishiyama,
     Chem. Eur. J. 2012, 18, 3153-3156.      DOI: 10.1002/chem.201103697


5 (MS; Dr. K. Oyama).
    H. Takaba, H. Omachi, Y. Yamamoto, J. Bouffard, K. Itami,
     Angew. Chem. Int. Ed. 2009, 48, 6112-6116.      DOI:10.1002/anie.200902617


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4 (Dr. K. Oyama for his assistance with the ESITOFMS measurement.)
    "Mechanism of Asymmetric Hydrogenation of Ketones Catalyzed by BINAP/1,2-Diamine-Ruthenium(II) Complexes"
    C. A. Sandoval, T. Ohkuma, K. Muniz, R. Noyori*
    J. Am. Chem. Soc. 2003, 125, 13490-13503.      DOI: 10.1021/ol026443k.
3 (We gratefully acknowledge Mr. Kin-ichi Oyama (Chemical Instrument Center of Nagoya University)
        for the measurement of high-resolution mass spectra.)
    "Simple Synthesis of r-Hydroxyamino Carbonyl Compounds: New Scope of the Nitroso Aldol Reaction"
    Norie Momiyama and Hisashi Yamamoto*
    Org. Lett. 2002, 4, 3579-3582.      DOI:10.1021/ja030272c
2 (We thank Mr. Kin-ichi Oyama (Chemical Instrument Center of Nagoya University) for measurement of ESI mass spectra.)
    "Lewis Acid Promoted, O-Selective, Nucleophilic Addition of Silyl Enol Ethers to N=O bonds"
    Norie Momiyama and Hisashi Yamamoto*
    Angew. Chem. Int. Ed. 2002, 41, 2986-2988.      DOI: 10.1002/anie.200902617.
1 (We are grateful to Mr. Kin-ichi Oyama of Nagoya University for measuring MS spectra.)
    "Molecular Design of Glutathione-derived Biochemical Probes targeting the GS.X Pump"
    Kyoji Furuta, Kellchiro Tomokiyo, M. Tien Kuo, Toshihisa Ishikawa, Masaaki Suzuki*
    Tetrahedron 55 (1999)7529-7540      doi.org/10.1016/S0040-4020(99)00375-0.






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