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Smelting of Scandium by Microwave Irradiation.

Materials (Basel, Switzerland)

Fujii S, Tsubaki S, Inazu N, Suzuki E, Wada Y.
PMID: 28953241
Materials (Basel). 2017 Sep 27;10(10). doi: 10.3390/ma10101138.

Scandium is being explored as an alloying element for aluminum alloys, which are gaining importance as high-performance lightweight structural alloys in the transportation industry. A few years ago, Sc was also found to be suitable for use in electrical...

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Fujii S, Tsubaki S, Inazu N, et al. Smelting of Scandium by Microwave Irradiation. Materials (Basel). 2017;10(10)doi: 10.3390/ma10101138.
Fujii, S., Tsubaki, S., Inazu, N., Suzuki, E., & Wada, Y. (2017). Smelting of Scandium by Microwave Irradiation. Materials (Basel, Switzerland), 10(10), . https://doi.org/10.3390/ma10101138
Fujii, Satoshi, et al. "Smelting of Scandium by Microwave Irradiation." Materials (Basel, Switzerland) vol. 10,10 (2017). doi: https://doi.org/10.3390/ma10101138
Fujii S, Tsubaki S, Inazu N, Suzuki E, Wada Y. Smelting of Scandium by Microwave Irradiation. Materials (Basel). 2017 Sep 27;10(10). doi: 10.3390/ma10101138. PMID: 28953241; PMCID: PMC5666944.
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Complications Associated With Spine Surgery in Patients Aged 80 Years or Older: Japan Association of Spine Surgeons with Ambition (JASA) Multicenter Study.

Global spine journal

Kobayashi K, Imagama S, Ando K, Ishiguro N, Yamashita M, Eguchi Y, Matsumoto M, Ishii K, Hikata T, Seki S, Terai H, Suzuki A, Tamai K, Aramomi M, Ishikawa T, Kimura A, Inoue H, Inoue G, Miyagi M, Saito W, Yamada K, Hongo M, Nishimura H, Suzuki H, Nakano A, Watanabe K, Chikuda H, Ohya J, Aoki Y, Shimizu M, Futatsugi T, Mukaiyama K, Hasegawa M, Kiyasu K, Iizuka H, Iizuka Y, Kobayashi R, Nishida K, Kakutani K, Nakajima H, Murakami H, Demura S, Kato S, Yoshioka K, Namikawa T, Watanabe K, Nakanishi K, Nakagawa Y, Yoshimoto M, Fujiwara H, Nishida N, Imajo Y, Yamazaki M, Sakane M, Abe T, Fujii K, Kaito T, Furuya T, Orita S, Ohtori S.
PMID: 28989842
Global Spine J. 2017 Oct;7(7):636-641. doi: 10.1177/2192568217716144. Epub 2017 Jul 20.

STUDY DESIGN: Retrospective study of registry data.OBJECTIVES: Aging of society and recent advances in surgical techniques and general anesthesia have increased the demand for spinal surgery in elderly patients. Many complications have been described in elderly patients, but a...

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Kobayashi K, Imagama S, Ando K, et al. Complications Associated With Spine Surgery in Patients Aged 80 Years or Older: Japan Association of Spine Surgeons with Ambition (JASA) Multicenter Study. Global Spine J. 2017;7(7):636-641doi: 10.1177/2192568217716144.
Kobayashi, K., Imagama, S., Ando, K., Ishiguro, N., Yamashita, M., Eguchi, Y., Matsumoto, M., Ishii, K., Hikata, T., Seki, S., Terai, H., Suzuki, A., Tamai, K., Aramomi, M., Ishikawa, T., Kimura, A., Inoue, H., Inoue, G., Miyagi, M., Saito, W., Yamada, K., Hongo, M., Nishimura, H., Suzuki, H., Nakano, A., Watanabe, K., Chikuda, H., Ohya, J., Aoki, Y., Shimizu, M., Futatsugi, T., Mukaiyama, K., Hasegawa, M., Kiyasu, K., Iizuka, H., Iizuka, Y., Kobayashi, R., Nishida, K., Kakutani, K., Nakajima, H., Murakami, H., Demura, S., Kato, S., Yoshioka, K., Namikawa, T., Watanabe, K., Nakanishi, K., Nakagawa, Y., Yoshimoto, M., Fujiwara, H., Nishida, N., Imajo, Y., Yamazaki, M., Sakane, M., Abe, T., Fujii, K., Kaito, T., Furuya, T., Orita, S., & Ohtori, S. (2017). Complications Associated With Spine Surgery in Patients Aged 80 Years or Older: Japan Association of Spine Surgeons with Ambition (JASA) Multicenter Study. Global spine journal, 7(7), 636-641. https://doi.org/10.1177/2192568217716144
Kobayashi, Kazuyoshi, et al. "Complications Associated With Spine Surgery in Patients Aged 80 Years or Older: Japan Association of Spine Surgeons with Ambition (JASA) Multicenter Study." Global spine journal vol. 7,7 (2017): 636-641. doi: https://doi.org/10.1177/2192568217716144
Kobayashi K, Imagama S, Ando K, Ishiguro N, Yamashita M, Eguchi Y, Matsumoto M, Ishii K, Hikata T, Seki S, Terai H, Suzuki A, Tamai K, Aramomi M, Ishikawa T, Kimura A, Inoue H, Inoue G, Miyagi M, Saito W, Yamada K, Hongo M, Nishimura H, Suzuki H, Nakano A, Watanabe K, Chikuda H, Ohya J, Aoki Y, Shimizu M, Futatsugi T, Mukaiyama K, Hasegawa M, Kiyasu K, Iizuka H, Iizuka Y, Kobayashi R, Nishida K, Kakutani K, Nakajima H, Murakami H, Demura S, Kato S, Yoshioka K, Namikawa T, Watanabe K, Nakanishi K, Nakagawa Y, Yoshimoto M, Fujiwara H, Nishida N, Imajo Y, Yamazaki M, Sakane M, Abe T, Fujii K, Kaito T, Furuya T, Orita S, Ohtori S. Complications Associated With Spine Surgery in Patients Aged 80 Years or Older: Japan Association of Spine Surgeons with Ambition (JASA) Multicenter Study. Global Spine J. 2017 Oct;7(7):636-641. doi: 10.1177/2192568217716144. Epub 2017 Jul 20. PMID: 28989842; PMCID: PMC5624380.
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Evaluation of nanodispersion of iron oxides using various polymers.

Indian journal of pharmaceutical sciences

Tanaka Y, Ueyama H, Ogata M, Daikoku T, Morimoto M, Kitagawa A, Imajo Y, Tahara T, Inkyo M, Yamaguchi N, Nagata S.
PMID: 24799739
Indian J Pharm Sci. 2014 Jan;76(1):54-61.

In order to create Fe2O3 and Fe2O3·H2O nanoparticles, various polymers were used as dispersing agents, and the resulting effects on the dispersibility and nanoparticulation of the iron oxides were evaluated. It was revealed that not only the solution viscosity...

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Tanaka Y, Ueyama H, Ogata M, et al. Evaluation of nanodispersion of iron oxides using various polymers. Indian J Pharm Sci. 2014;76(1):54-61
Tanaka, Y., Ueyama, H., Ogata, M., Daikoku, T., Morimoto, M., Kitagawa, A., Imajo, Y., Tahara, T., Inkyo, M., Yamaguchi, N., & Nagata, S. (2014). Evaluation of nanodispersion of iron oxides using various polymers. Indian journal of pharmaceutical sciences, 76(1), 54-61.
Tanaka, Y, et al. "Evaluation of nanodispersion of iron oxides using various polymers." Indian journal of pharmaceutical sciences vol. 76,1 (2014): 54-61.
Tanaka Y, Ueyama H, Ogata M, Daikoku T, Morimoto M, Kitagawa A, Imajo Y, Tahara T, Inkyo M, Yamaguchi N, Nagata S. Evaluation of nanodispersion of iron oxides using various polymers. Indian J Pharm Sci. 2014 Jan;76(1):54-61. PMID: 24799739; PMCID: PMC4007256.
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A study of C-F...M(+) interaction: metal complexes of fluorine-containing cage compounds.

Journal of the American Chemical Society

Takemura H, Nakashima S, Kon N, Yasutake M, Shinmyozu T, Inazu T.
PMID: 11562211
J Am Chem Soc. 2001 Sep 26;123(38):9293-8. doi: 10.1021/ja0043587.

The C-F...M(+) interaction was investigated by observation of the NMR spectroscopic changes and complexation studies between metal cations and the cage compounds 1 and 2 which have fluorobenzene units as donor atoms. As a result, the interaction was detected...

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Takemura H, Nakashima S, Kon N, et al. A study of C-F...M(+) interaction: metal complexes of fluorine-containing cage compounds. J Am Chem Soc. 2001;123(38):9293-8doi: 10.1021/ja0043587.
Takemura, H., Nakashima, S., Kon, N., Yasutake, M., Shinmyozu, T., & Inazu, T. (2001). A study of C-F...M(+) interaction: metal complexes of fluorine-containing cage compounds. Journal of the American Chemical Society, 123(38), 9293-8. https://doi.org/10.1021/ja0043587
Takemura, H, et al. "A study of C-F...M(+) interaction: metal complexes of fluorine-containing cage compounds." Journal of the American Chemical Society vol. 123,38 (2001): 9293-8. doi: https://doi.org/10.1021/ja0043587
Takemura H, Nakashima S, Kon N, Yasutake M, Shinmyozu T, Inazu T. A study of C-F...M(+) interaction: metal complexes of fluorine-containing cage compounds. J Am Chem Soc. 2001 Sep 26;123(38):9293-8. doi: 10.1021/ja0043587. PMID: 11562211.
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The efficacy of diagnostic procedures in medical-surgical pathology of the salivary glands. .

Medicina oral : organo oficial de la Sociedad Espanola de Medicina Oral y de la Academia Iberoamericana de Patologia y Medicina Bucal

Santamaria J, Irazu L, Arteagoffla I, Alonso J, Romo L, Alvarez J, Esteban S, Santamaria G, Landa S.
PMID: 11507557
Med Oral. 2000 May-Jul;5(3):198-207.

No abstract available.

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Santamaria J, Irazu L, Arteagoffla I, et al. The efficacy of diagnostic procedures in medical-surgical pathology of the salivary glands. . Med Oral. 2000;5(3):198-207
Santamaria, J., Irazu, L., Arteagoffla, I., Alonso, J., Romo, L., Alvarez, J., Esteban, S., Santamaria, G., & Landa, S. (2000). The efficacy of diagnostic procedures in medical-surgical pathology of the salivary glands. . Medicina oral : organo oficial de la Sociedad Espanola de Medicina Oral y de la Academia Iberoamericana de Patologia y Medicina Bucal, 5(3), 198-207.
Santamaria, J., et al. "The efficacy of diagnostic procedures in medical-surgical pathology of the salivary glands. ." Medicina oral : organo oficial de la Sociedad Espanola de Medicina Oral y de la Academia Iberoamericana de Patologia y Medicina Bucal vol. 5,3 (2000): 198-207.
Santamaria J, Irazu L, Arteagoffla I, Alonso J, Romo L, Alvarez J, Esteban S, Santamaria G, Landa S. The efficacy of diagnostic procedures in medical-surgical pathology of the salivary glands. . Med Oral. 2000 May-Jul;5(3):198-207. PMID: 11507557.
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Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction.

The Journal of organic chemistry

Kon N, Takemura H, Otsuka K, Tanoue K, Nakashima S, Yasutake M, Tani K, Kimoto J, Shinmyozu T, Inazu T.
PMID: 10864755
J Org Chem. 2000 Jun 16;65(12):3708-15. doi: 10.1021/jo991911y.

Macropolycyclic cage compounds were synthesized by a direct reaction between diamines and bis(bromomethyl) compounds. The procedure for constructing the polycyclic cage structure is simple and straightforward. The macropolycyclic compounds obtainable from this cyclization procedure are three-dimensional cage compounds, and...

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Kon N, Takemura H, Otsuka K, et al. Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction. J Org Chem. 2000;65(12):3708-15doi: 10.1021/jo991911y.
Kon, N., Takemura, H., Otsuka, K., Tanoue, K., Nakashima, S., Yasutake, M., Tani, K., Kimoto, J., Shinmyozu, T., & Inazu, T. (2000). Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction. The Journal of organic chemistry, 65(12), 3708-15. https://doi.org/10.1021/jo991911y
Kon, et al. "Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction." The Journal of organic chemistry vol. 65,12 (2000): 3708-15. doi: https://doi.org/10.1021/jo991911y
Kon N, Takemura H, Otsuka K, Tanoue K, Nakashima S, Yasutake M, Tani K, Kimoto J, Shinmyozu T, Inazu T. Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction. J Org Chem. 2000 Jun 16;65(12):3708-15. doi: 10.1021/jo991911y. PMID: 10864755.
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Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1).

The Journal of organic chemistry

Harusawa S, Murai Y, Moriyama H, Imazu T, Ohishi H, Yoneda R, Kurihara T.
PMID: 11667345
J Org Chem. 1996 Jun 26;61(13):4405-4411. doi: 10.1021/jo952136z.

A synthetic route to 4(5)-(beta-D-ribofuranosyl)imidazole (1), starting from 2,3,5-tri-O-benzyl-D-ribose (5), was developed via a Mitsunobu cyclization. Reaction of 5 with the lithium salt of bis-protected imidazole afforded the corresponding 5-ribosylimidazole 7RS. Hydrolysis of 7RS gave a 1:1 mixture of...

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Harusawa S, Murai Y, Moriyama H, et al. Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1). J Org Chem. 1996;61(13):4405-4411doi: 10.1021/jo952136z.
Harusawa, S., Murai, Y., Moriyama, H., Imazu, T., Ohishi, H., Yoneda, R., & Kurihara, T. (1996). Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1). The Journal of organic chemistry, 61(13), 4405-4411. https://doi.org/10.1021/jo952136z
Harusawa, Shinya, et al. "Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1)." The Journal of organic chemistry vol. 61,13 (1996): 4405-4411. doi: https://doi.org/10.1021/jo952136z
Harusawa S, Murai Y, Moriyama H, Imazu T, Ohishi H, Yoneda R, Kurihara T. Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1). J Org Chem. 1996 Jun 26;61(13):4405-4411. doi: 10.1021/jo952136z. PMID: 11667345.
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Asymmetric baeyer-villiger reaction with hydrogen peroxide catalyzed by a novel planar-chiral bisflavin.

Angewandte Chemie (International ed. in English)

Murahashi S, Ono S, Imada Y.
PMID: 12203594
Angew Chem Int Ed Engl. 2002 Jul 02;41(13):2366-8. doi: 10.1002/1521-3773(20020703)41:13<2366::AID-ANIE2366>3.0.CO;2-S.

No abstract available.

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Murahashi S, Ono S, Imada Y. Asymmetric baeyer-villiger reaction with hydrogen peroxide catalyzed by a novel planar-chiral bisflavin. Angew Chem Int Ed Engl. 2002;41(13):2366-8doi: 10.1002/1521-3773(20020703)41:13<2366::AID-ANIE2366>3.0.CO;2-S.
Murahashi, S., Ono, S., & Imada, Y. (2002). Asymmetric baeyer-villiger reaction with hydrogen peroxide catalyzed by a novel planar-chiral bisflavin. Angewandte Chemie (International ed. in English), 41(13), 2366-8. https://doi.org/10.1002/1521-3773(20020703)41:13<2366::AID-ANIE2366>3.0.CO;2-S
Murahashi, Shun-Ichi, et al. "Asymmetric baeyer-villiger reaction with hydrogen peroxide catalyzed by a novel planar-chiral bisflavin." Angewandte Chemie (International ed. in English) vol. 41,13 (2002): 2366-8. doi: https://doi.org/10.1002/1521-3773(20020703)41:13<2366::AID-ANIE2366>3.0.CO;2-S
Murahashi S, Ono S, Imada Y. Asymmetric baeyer-villiger reaction with hydrogen peroxide catalyzed by a novel planar-chiral bisflavin. Angew Chem Int Ed Engl. 2002 Jul 02;41(13):2366-8. doi: 10.1002/1521-3773(20020703)41:13<2366::AID-ANIE2366>3.0.CO;2-S. PMID: 12203594.
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Gastritis cystica polyposa associated with a gastric stump carcinoma, with special reference to cell kinetics and p53 gene aberrations.

Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association

Ochiai M, Matsubara T, Zhi LZ, Funabiki T, Sakurai Y, Hasegawa S, Imazu H, Suganuma M.
PMID: 11984732
Gastric Cancer. 2000 Dec 27;3(3):165-170. doi: 10.1007/pl00011713.

We report a case of gastritis cystica polyposa (GCP) that developed in association with a small stump carcinoma. The patient had had distal gastrectomy for peptic ulcer 33 years prior to the present illness. Total gastrectomy was carried out...

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Ochiai M, Matsubara T, Zhi LZ, et al. Gastritis cystica polyposa associated with a gastric stump carcinoma, with special reference to cell kinetics and p53 gene aberrations. Gastric Cancer. 2000;3(3):165-170doi: 10.1007/pl00011713.
Ochiai, M., Matsubara, T., Zhi, L. Z., Funabiki, T., Sakurai, Y., Hasegawa, S., Imazu, H., & Suganuma, M. (2000). Gastritis cystica polyposa associated with a gastric stump carcinoma, with special reference to cell kinetics and p53 gene aberrations. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 3(3), 165-170. https://doi.org/10.1007/pl00011713
Ochiai, Masahiro, et al. "Gastritis cystica polyposa associated with a gastric stump carcinoma, with special reference to cell kinetics and p53 gene aberrations." Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association vol. 3,3 (2000): 165-170. doi: https://doi.org/10.1007/pl00011713
Ochiai M, Matsubara T, Zhi LZ, Funabiki T, Sakurai Y, Hasegawa S, Imazu H, Suganuma M. Gastritis cystica polyposa associated with a gastric stump carcinoma, with special reference to cell kinetics and p53 gene aberrations. Gastric Cancer. 2000 Dec 27;3(3):165-170. doi: 10.1007/pl00011713. PMID: 11984732.
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Fluorous oligosaccharide synthesis using a novel fluorous protective group.

Organic letters

Miura T, Hirose Y, Ohmae M, Inazu T.
PMID: 11720576
Org Lett. 2001 Nov 29;3(24):3947-50. doi: 10.1021/ol016838o.

The Bfp (bisfluorous chain type propanoyl) group, a novel fluorous protecting reagent, was able to be prepared easily. The Bfp group was readily introduced to carbohydrate, was removed in high yield, and was recyclable after cleavage. Use of the...

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Miura T, Hirose Y, Ohmae M, et al. Fluorous oligosaccharide synthesis using a novel fluorous protective group. Org Lett. 2001;3(24):3947-50doi: 10.1021/ol016838o.
Miura, T., Hirose, Y., Ohmae, M., & Inazu, T. (2001). Fluorous oligosaccharide synthesis using a novel fluorous protective group. Organic letters, 3(24), 3947-50. https://doi.org/10.1021/ol016838o
Miura, T, et al. "Fluorous oligosaccharide synthesis using a novel fluorous protective group." Organic letters vol. 3,24 (2001): 3947-50. doi: https://doi.org/10.1021/ol016838o
Miura T, Hirose Y, Ohmae M, Inazu T. Fluorous oligosaccharide synthesis using a novel fluorous protective group. Org Lett. 2001 Nov 29;3(24):3947-50. doi: 10.1021/ol016838o. PMID: 11720576.
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An aerobic, organocatalytic, and chemoselective method for Baeyer-Villiger oxidation.

Angewandte Chemie (International ed. in English)

Imada Y, Iida H, Murahashi S, Naota T.
PMID: 15693045
Angew Chem Int Ed Engl. 2005 Mar 04;44(11):1704-6. doi: 10.1002/anie.200462429.

No abstract available.

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Imada Y, Iida H, Murahashi S, et al. An aerobic, organocatalytic, and chemoselective method for Baeyer-Villiger oxidation. Angew Chem Int Ed Engl. 2005;44(11):1704-6doi: 10.1002/anie.200462429.
Imada, Y., Iida, H., Murahashi, S., & Naota, T. (2005). An aerobic, organocatalytic, and chemoselective method for Baeyer-Villiger oxidation. Angewandte Chemie (International ed. in English), 44(11), 1704-6. https://doi.org/10.1002/anie.200462429
Imada, Yasushi, et al. "An aerobic, organocatalytic, and chemoselective method for Baeyer-Villiger oxidation." Angewandte Chemie (International ed. in English) vol. 44,11 (2005): 1704-6. doi: https://doi.org/10.1002/anie.200462429
Imada Y, Iida H, Murahashi S, Naota T. An aerobic, organocatalytic, and chemoselective method for Baeyer-Villiger oxidation. Angew Chem Int Ed Engl. 2005 Mar 04;44(11):1704-6. doi: 10.1002/anie.200462429. PMID: 15693045.
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Catalytic transformation of methane over in-loaded ZSM-5 zeolite in the presence of ethene.

The journal of physical chemistry. B

Baba T, Abe Y, Nomoto K, Inazu K, Echizen T, Ishikawa A, Murai K.
PMID: 16851490
J Phys Chem B. 2005 Mar 10;109(9):4263-8. doi: 10.1021/jp045640t.

Methane is shown to react with ethene over In-loaded ZSM-5 to higher hydrocarbons such as propene and toluene at around 673 K. Such methane conversion is not catalyzed by proton-exchanged ZSM-5 (H-ZSM-5) under the same conditions, only C2H4 being...

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Baba T, Abe Y, Nomoto K, et al. Catalytic transformation of methane over in-loaded ZSM-5 zeolite in the presence of ethene. J Phys Chem B. 2005;109(9):4263-8doi: 10.1021/jp045640t.
Baba, T., Abe, Y., Nomoto, K., Inazu, K., Echizen, T., Ishikawa, A., & Murai, K. (2005). Catalytic transformation of methane over in-loaded ZSM-5 zeolite in the presence of ethene. The journal of physical chemistry. B, 109(9), 4263-8. https://doi.org/10.1021/jp045640t
Baba, Toshihide, et al. "Catalytic transformation of methane over in-loaded ZSM-5 zeolite in the presence of ethene." The journal of physical chemistry. B vol. 109,9 (2005): 4263-8. doi: https://doi.org/10.1021/jp045640t
Baba T, Abe Y, Nomoto K, Inazu K, Echizen T, Ishikawa A, Murai K. Catalytic transformation of methane over in-loaded ZSM-5 zeolite in the presence of ethene. J Phys Chem B. 2005 Mar 10;109(9):4263-8. doi: 10.1021/jp045640t. PMID: 16851490.
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