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Wide-ranging host capability of a Pd(II)-linked M2L4 molecular capsule with an anthracene shell.

Chemistry (Weinheim an der Bergstrasse, Germany)

Kishi N, Li Z, Sei Y, Akita M, Yoza K, Siegel JS, Yoshizawa M.
PMID: 23508693
Chemistry. 2013 May 10;19(20):6313-20. doi: 10.1002/chem.201204010. Epub 2013 Mar 18.

This article reports that an M2L4 molecular capsule is capable of encapsulating various neutral molecules in quantitative yields. The capsule was obtained as a single product by mixing a small number of components; two Pd(II) ions and four bent...

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Kishi N, Li Z, Sei Y, et al. Wide-ranging host capability of a Pd(II)-linked M2L4 molecular capsule with an anthracene shell. Chemistry. 2013;19(20):6313-20doi: 10.1002/chem.201204010.
Kishi, N., Li, Z., Sei, Y., Akita, M., Yoza, K., Siegel, J. S., & Yoshizawa, M. (2013). Wide-ranging host capability of a Pd(II)-linked M2L4 molecular capsule with an anthracene shell. Chemistry (Weinheim an der Bergstrasse, Germany), 19(20), 6313-20. https://doi.org/10.1002/chem.201204010
Kishi, Norifumi, et al. "Wide-ranging host capability of a Pd(II)-linked M2L4 molecular capsule with an anthracene shell." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,20 (2013): 6313-20. doi: https://doi.org/10.1002/chem.201204010
Kishi N, Li Z, Sei Y, Akita M, Yoza K, Siegel JS, Yoshizawa M. Wide-ranging host capability of a Pd(II)-linked M2L4 molecular capsule with an anthracene shell. Chemistry. 2013 May 10;19(20):6313-20. doi: 10.1002/chem.201204010. Epub 2013 Mar 18. PMID: 23508693.
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Safety, tolerability, pharmacokinetics and pharmacodynamics of belimumab in Japanese patients with mild-to-moderate systemic lupus erythematosus.

Journal of drug assessment

Yamada M, Akita M, Nakagawa T, Takahashi N, Endo A, Yoshida P.
PMID: 27536436
J Drug Assess. 2013 Apr 12;2(1):40-8. doi: 10.3109/21556660.2013.792823. eCollection 2013.

OBJECTIVES: Belimumab, an anti-B lymphocyte stimulator (BLyS) human monoclonal antibody, was approved in the United States, Canada and European Union for the treatment of the patients with systemic lupus erythematosus (SLE). However, belimumab had not been evaluated in Japanese...

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Yamada M, Akita M, Nakagawa T, et al. Safety, tolerability, pharmacokinetics and pharmacodynamics of belimumab in Japanese patients with mild-to-moderate systemic lupus erythematosus. J Drug Assess. 2013;2(1):40-8doi: 10.3109/21556660.2013.792823.
Yamada, M., Akita, M., Nakagawa, T., Takahashi, N., Endo, A., & Yoshida, P. (2013). Safety, tolerability, pharmacokinetics and pharmacodynamics of belimumab in Japanese patients with mild-to-moderate systemic lupus erythematosus. Journal of drug assessment, 2(1), 40-8. https://doi.org/10.3109/21556660.2013.792823
Yamada, Masanori, et al. "Safety, tolerability, pharmacokinetics and pharmacodynamics of belimumab in Japanese patients with mild-to-moderate systemic lupus erythematosus." Journal of drug assessment vol. 2,1 (2013): 40-8. doi: https://doi.org/10.3109/21556660.2013.792823
Yamada M, Akita M, Nakagawa T, Takahashi N, Endo A, Yoshida P. Safety, tolerability, pharmacokinetics and pharmacodynamics of belimumab in Japanese patients with mild-to-moderate systemic lupus erythematosus. J Drug Assess. 2013 Apr 12;2(1):40-8. doi: 10.3109/21556660.2013.792823. eCollection 2013. PMID: 27536436; PMCID: PMC4937663.
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Selective Oxidation of 2-Methylnaphthalene to 2-Methyl-l-naphthol by Rhodococcus sp. M192.

Bioscience, biotechnology, and biochemistry

Taguchi H, Kita S, Kobayashi M, Tan Y.
PMID: 27281139
Biosci Biotechnol Biochem. 1996 Jan;60(5):769-72. doi: 10.1271/bbb.60.769.

About 6000 isolates of microorganisms assimilating methylketones (C3-C6) were tested for their selective oxidation of 2-methylnaphthalene to 2-methyl-1-naphthol. Strain M192 was the highest 2-methyl-1-naphthol producer and was classified as the genus Rhodococcus. The optimal conditions for the site-specific oxidation...

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Taguchi H, Kita S, Kobayashi M, et al. Selective Oxidation of 2-Methylnaphthalene to 2-Methyl-l-naphthol by Rhodococcus sp. M192. Biosci Biotechnol Biochem. 1996;60(5):769-72doi: 10.1271/bbb.60.769.
Taguchi, H., Kita, S., Kobayashi, M., & Tan, Y. (1996). Selective Oxidation of 2-Methylnaphthalene to 2-Methyl-l-naphthol by Rhodococcus sp. M192. Bioscience, biotechnology, and biochemistry, 60(5), 769-72. https://doi.org/10.1271/bbb.60.769
Taguchi, H, et al. "Selective Oxidation of 2-Methylnaphthalene to 2-Methyl-l-naphthol by Rhodococcus sp. M192." Bioscience, biotechnology, and biochemistry vol. 60,5 (1996): 769-72. doi: https://doi.org/10.1271/bbb.60.769
Taguchi H, Kita S, Kobayashi M, Tan Y. Selective Oxidation of 2-Methylnaphthalene to 2-Methyl-l-naphthol by Rhodococcus sp. M192. Biosci Biotechnol Biochem. 1996 Jan;60(5):769-72. doi: 10.1271/bbb.60.769. PMID: 27281139.
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A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water.

Chemical communications (Cambridge, England)

Suzuki A, Kondo K, Sei Y, Akita M, Yoshizawa M.
PMID: 26804491
Chem Commun (Camb). 2016 Feb 21;52(15):3151-4. doi: 10.1039/c5cc09647b.

A new molecular capsule with a flexible fluorescent shell was formed by the quantitative self-complementary assembly of amphiphilic, U-shaped polyaromatic subunits in water. The capsule can fully encapsulate a variety of non-fluorescent monoterpene compounds (e.g., menthone, menthol, and p-menthane)...

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Suzuki A, Kondo K, Sei Y, et al. A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water. Chem Commun (Camb). 2016;52(15):3151-4doi: 10.1039/c5cc09647b.
Suzuki, A., Kondo, K., Sei, Y., Akita, M., & Yoshizawa, M. (2016). A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water. Chemical communications (Cambridge, England), 52(15), 3151-4. https://doi.org/10.1039/c5cc09647b
Suzuki, Akira, et al. "A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water." Chemical communications (Cambridge, England) vol. 52,15 (2016): 3151-4. doi: https://doi.org/10.1039/c5cc09647b
Suzuki A, Kondo K, Sei Y, Akita M, Yoshizawa M. A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water. Chem Commun (Camb). 2016 Feb 21;52(15):3151-4. doi: 10.1039/c5cc09647b. PMID: 26804491.
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Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling.

Organic & biomolecular chemistry

Morimoto K, Ohnishi Y, Koseki D, Nakamura A, Dohi T, Kita Y.
PMID: 27722732
Org Biomol Chem. 2016 Sep 26;14(38):8947-8951. doi: 10.1039/c6ob01764a.

Pyrrole-aryl derivatives are important due to their unique biological activities in medicinal chemistry. We now report a new oxidative biaryl coupling for pyrroles and indoles toward various arenes using a hypervalent iodine reagent and an appropriate stabilizer for pyrrolyl...

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Morimoto K, Ohnishi Y, Koseki D, et al. Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling. Org Biomol Chem. 2016;14(38):8947-8951doi: 10.1039/c6ob01764a.
Morimoto, K., Ohnishi, Y., Koseki, D., Nakamura, A., Dohi, T., & Kita, Y. (2016). Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling. Organic & biomolecular chemistry, 14(38), 8947-8951. https://doi.org/10.1039/c6ob01764a
Morimoto, Koji, et al. "Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling." Organic & biomolecular chemistry vol. 14,38 (2016): 8947-8951. doi: https://doi.org/10.1039/c6ob01764a
Morimoto K, Ohnishi Y, Koseki D, Nakamura A, Dohi T, Kita Y. Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling. Org Biomol Chem. 2016 Sep 26;14(38):8947-8951. doi: 10.1039/c6ob01764a. PMID: 27722732.
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Non-Inflammatory Destructive Periodontal Disease.

The open dentistry journal

José Ricardo Kina, Yumi Umeda Suzuki T, Fumico Umeda Kina E, Kina J, Kina M.
PMID: 27053968
Open Dent J. 2016 Mar 10;10:50-7. doi: 10.2174/1874210601610010050. eCollection 2016.

BACKGROUND: Non-Inflammatory Destructive Periodontal Disease (NIDPD), is a severe destructive periodontal disease, that is characterized by the attachment loss and alveolar bone loss, without signs of the gingival inflammation, and the periodontal pocket development.OBJECTIVE: Despite the fact that various...

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José Ricardo Kina, Yumi Umeda Suzuki T, Fumico Umeda Kina E, et al. Non-Inflammatory Destructive Periodontal Disease. Open Dent J. 2016;10:50-7doi: 10.2174/1874210601610010050.
José Ricardo Kina, Yumi Umeda Suzuki, T., Fumico Umeda Kina, E., Kina, J., & Kina, M. (2016). Non-Inflammatory Destructive Periodontal Disease. The open dentistry journal, 1050-7. https://doi.org/10.2174/1874210601610010050
José Ricardo Kina, et al. "Non-Inflammatory Destructive Periodontal Disease." The open dentistry journal vol. 10 (2016): 50-7. doi: https://doi.org/10.2174/1874210601610010050
José Ricardo Kina, Yumi Umeda Suzuki T, Fumico Umeda Kina E, Kina J, Kina M. Non-Inflammatory Destructive Periodontal Disease. Open Dent J. 2016 Mar 10;10:50-7. doi: 10.2174/1874210601610010050. eCollection 2016. PMID: 27053968; PMCID: PMC4787315.
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Bronchiolitis and bacteraemia caused by Burkholderia gladioli in a non-lung transplantation patient.

New microbes and new infections

Imataki O, Kita N, Nakayama-Imaohji H, Kida JI, Kuwahara T, Uemura M.
PMID: 25566397
New Microbes New Infect. 2014 Nov;2(6):175-6. doi: 10.1002/nmi2.64. Epub 2014 Sep 25.

No abstract available.

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Imataki O, Kita N, Nakayama-Imaohji H, et al. Bronchiolitis and bacteraemia caused by Burkholderia gladioli in a non-lung transplantation patient. New Microbes New Infect. 2014;2(6):175-6doi: 10.1002/nmi2.64.
Imataki, O., Kita, N., Nakayama-Imaohji, H., Kida, J. I., Kuwahara, T., & Uemura, M. (2014). Bronchiolitis and bacteraemia caused by Burkholderia gladioli in a non-lung transplantation patient. New microbes and new infections, 2(6), 175-6. https://doi.org/10.1002/nmi2.64
Imataki, O, et al. "Bronchiolitis and bacteraemia caused by Burkholderia gladioli in a non-lung transplantation patient." New microbes and new infections vol. 2,6 (2014): 175-6. doi: https://doi.org/10.1002/nmi2.64
Imataki O, Kita N, Nakayama-Imaohji H, Kida JI, Kuwahara T, Uemura M. Bronchiolitis and bacteraemia caused by Burkholderia gladioli in a non-lung transplantation patient. New Microbes New Infect. 2014 Nov;2(6):175-6. doi: 10.1002/nmi2.64. Epub 2014 Sep 25. PMID: 25566397; PMCID: PMC4265050.
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Phthalimide Compounds Containing a Trifluoromethylphenyl Group and Electron-Donating Aryl Groups: Color-Tuning and Enhancement of Triboluminescence.

The Journal of organic chemistry

Nishida J, Ohura H, Kita Y, Hasegawa H, Kawase T, Takada N, Sato H, Sei Y, Yamashita Y.
PMID: 26652502
J Org Chem. 2016 Jan 15;81(2):433-41. doi: 10.1021/acs.joc.5b02191. Epub 2015 Dec 24.

Trifluoromethylphenyl-substituted phthalimide derivatives favorably form triboluminescence (TL) active noncentrosymmetric crystals. Oligothienyl-, oligophenyl-, and naphthyl-substituted phthalimide derivatives were successfully developed as a series of metal free TL compounds. X-ray crystal structure analyses of bithienyl and naphthyl derivatives revealed noncentrosymmetric layer...

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Nishida J, Ohura H, Kita Y, et al. Phthalimide Compounds Containing a Trifluoromethylphenyl Group and Electron-Donating Aryl Groups: Color-Tuning and Enhancement of Triboluminescence. J Org Chem. 2015;81(2):433-41doi: 10.1021/acs.joc.5b02191.
Nishida, J., Ohura, H., Kita, Y., Hasegawa, H., Kawase, T., Takada, N., Sato, H., Sei, Y., & Yamashita, Y. (2016). Phthalimide Compounds Containing a Trifluoromethylphenyl Group and Electron-Donating Aryl Groups: Color-Tuning and Enhancement of Triboluminescence. The Journal of organic chemistry, 81(2), 433-41. https://doi.org/10.1021/acs.joc.5b02191
Nishida, Jun-ichi, et al. "Phthalimide Compounds Containing a Trifluoromethylphenyl Group and Electron-Donating Aryl Groups: Color-Tuning and Enhancement of Triboluminescence." The Journal of organic chemistry vol. 81,2 (2016): 433-41. doi: https://doi.org/10.1021/acs.joc.5b02191
Nishida J, Ohura H, Kita Y, Hasegawa H, Kawase T, Takada N, Sato H, Sei Y, Yamashita Y. Phthalimide Compounds Containing a Trifluoromethylphenyl Group and Electron-Donating Aryl Groups: Color-Tuning and Enhancement of Triboluminescence. J Org Chem. 2016 Jan 15;81(2):433-41. doi: 10.1021/acs.joc.5b02191. Epub 2015 Dec 24. PMID: 26652502.
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Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt.

Chemical communications (Cambridge, England)

Kita Y, Higuchi T, Mashima K.
PMID: 25112156
Chem Commun (Camb). 2014 Oct 04;50(76):11211-3. doi: 10.1039/c4cc04481a.

Addition of catalytic amounts of zinc salts facilitated the hydrogenation of amides catalyzed by a ruthenium complex bearing 2-(diphenylphosphino)ethanamine (L1). The combined catalytic system of the ruthenium complex [RuCl2(L1)2] with a zinc salt such as Zn(OCOCF3)2 mediated hydrogenation of...

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Kita Y, Higuchi T, Mashima K. Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt. Chem Commun (Camb). 2014;50(76):11211-3doi: 10.1039/c4cc04481a.
Kita, Y., Higuchi, T., & Mashima, K. (2014). Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt. Chemical communications (Cambridge, England), 50(76), 11211-3. https://doi.org/10.1039/c4cc04481a
Kita, Yusuke, et al. "Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt." Chemical communications (Cambridge, England) vol. 50,76 (2014): 11211-3. doi: https://doi.org/10.1039/c4cc04481a
Kita Y, Higuchi T, Mashima K. Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt. Chem Commun (Camb). 2014 Oct 04;50(76):11211-3. doi: 10.1039/c4cc04481a. PMID: 25112156.
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Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Ozawa H, Kosaka K, Kita T, Yoshikawa K, Haga MA.
PMID: 27010865
Chemistry. 2016 May 04;22(19):6575-82. doi: 10.1002/chem.201504678. Epub 2016 Mar 24.

We report the synthesis of a mixed-valence ruthenium complex, bearing pyrene moieties on one side of the ligands as anchor groups. Composites consisting of mixed-valence ruthenium complexes and SWNTs were prepared by noncovalent π-π interactions between the SWNT surface...

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Ozawa H, Kosaka K, Kita T, et al. Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes. Chemistry. 2016;22(19):6575-82doi: 10.1002/chem.201504678.
Ozawa, H., Kosaka, K., Kita, T., Yoshikawa, K., & Haga, M. A. (2016). Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes. Chemistry (Weinheim an der Bergstrasse, Germany), 22(19), 6575-82. https://doi.org/10.1002/chem.201504678
Ozawa, Hiroaki, et al. "Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,19 (2016): 6575-82. doi: https://doi.org/10.1002/chem.201504678
Ozawa H, Kosaka K, Kita T, Yoshikawa K, Haga MA. Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes. Chemistry. 2016 May 04;22(19):6575-82. doi: 10.1002/chem.201504678. Epub 2016 Mar 24. PMID: 27010865.
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Data in support of antioxidant activities of the non-extractable fraction of dried persimmon (Diospyros kaki Thunb.).

Data in brief

Matsumura Y, Ito T, Yano H, Kita E, Mikasa K, Okada M, Furutani A, Murono Y, Shibata M, Nishii Y, Kayano S.
PMID: 27547805
Data Brief. 2016 Jul 12;8:1247-54. doi: 10.1016/j.dib.2016.07.004. eCollection 2016 Sep.

This data article is related to the research article entitled, "Antioxidant potential in non-extractable fraction of dried persimmon (Diospyros kaki Thunb.)" (Matsumura et al., 2016) [1]. We investigated antioxidant activities of the non-extractable fraction of dried persimmon fruits in...

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Matsumura Y, Ito T, Yano H, et al. Data in support of antioxidant activities of the non-extractable fraction of dried persimmon (Diospyros kaki Thunb.). Data Brief. 2016;8:1247-54doi: 10.1016/j.dib.2016.07.004.
Matsumura, Y., Ito, T., Yano, H., Kita, E., Mikasa, K., Okada, M., Furutani, A., Murono, Y., Shibata, M., Nishii, Y., & Kayano, S. (2016). Data in support of antioxidant activities of the non-extractable fraction of dried persimmon (Diospyros kaki Thunb.). Data in brief, 81247-54. https://doi.org/10.1016/j.dib.2016.07.004
Matsumura, Yoko, et al. "Data in support of antioxidant activities of the non-extractable fraction of dried persimmon (Diospyros kaki Thunb.)." Data in brief vol. 8 (2016): 1247-54. doi: https://doi.org/10.1016/j.dib.2016.07.004
Matsumura Y, Ito T, Yano H, Kita E, Mikasa K, Okada M, Furutani A, Murono Y, Shibata M, Nishii Y, Kayano S. Data in support of antioxidant activities of the non-extractable fraction of dried persimmon (Diospyros kaki Thunb.). Data Brief. 2016 Jul 12;8:1247-54. doi: 10.1016/j.dib.2016.07.004. eCollection 2016 Sep. PMID: 27547805; PMCID: PMC4983141.
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An Ion-Responsive Pincer-Crown Ether Catalyst System for Rapid and Switchable Olefin Isomerization.

Angewandte Chemie (International ed. in English)

Kita MR, Miller AJM.
PMID: 28402591
Angew Chem Int Ed Engl. 2017 May 08;56(20):5498-5502. doi: 10.1002/anie.201701006. Epub 2017 Apr 12.

Rapid, selective, and highly controllable iridium-catalyzed allylbenzene isomerization is described, enabled by tunable hemilability based on alkali metal cation binding with a macrocyclic "pincer-crown ether" ligand. An inactive chloride-ligated complex can be activated by halide abstraction with sodium salts,...

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Kita MR, Miller AJM. An Ion-Responsive Pincer-Crown Ether Catalyst System for Rapid and Switchable Olefin Isomerization. Angew Chem Int Ed Engl. 2017;56(20):5498-5502doi: 10.1002/anie.201701006.
Kita, M. R., & Miller, A. J. M. (2017). An Ion-Responsive Pincer-Crown Ether Catalyst System for Rapid and Switchable Olefin Isomerization. Angewandte Chemie (International ed. in English), 56(20), 5498-5502. https://doi.org/10.1002/anie.201701006
Kita, Matthew R, and Miller, Alexander J M. "An Ion-Responsive Pincer-Crown Ether Catalyst System for Rapid and Switchable Olefin Isomerization." Angewandte Chemie (International ed. in English) vol. 56,20 (2017): 5498-5502. doi: https://doi.org/10.1002/anie.201701006
Kita MR, Miller AJM. An Ion-Responsive Pincer-Crown Ether Catalyst System for Rapid and Switchable Olefin Isomerization. Angew Chem Int Ed Engl. 2017 May 08;56(20):5498-5502. doi: 10.1002/anie.201701006. Epub 2017 Apr 12. PMID: 28402591.
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