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Characteristics of C-F Systems
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ed. by R. E. Banks, B. E. Smart, J. C. Tatlow, Plenum Press, New York
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B. E. Smart, Characteristics of C-F Systems, in Organofluorine Chemistry: Principles and Commercial Applications, ed. by R. E. Banks, B. E. Smart, J. C. Tatlow, Plenum Press, New York, 1994, p. 57.
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c) S. Kobayashi, S.-I. Shoda, H. Uyama, Adv. Polym. Sci. 1995, 121, 1.
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S. Kobayashi, T. Kiyosada, S.-I. Shoda, J. Am. Chem. Soc. 1996, 118, 13113.
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Ochiai, H.1
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Ochiai, H.1
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Kobayashi, S.3
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12
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33646447290
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note
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+ 206.0829, found 206.0830.
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13
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33646455817
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A. Makino, M. Ohmae, S. Kobayashi, Polym. Prepr. Jpn. 2001, 50, 998.
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Makino, A.1
Ohmae, M.2
Kobayashi, S.3
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14
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33646449730
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A. Makino, J. Sakamoto, M. Ohmae, S. Kobayashi, Polym. Prepr. Jpn. 2003, 52, 1049.
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Makino, A.1
Sakamoto, J.2
Ohmae, M.3
Kobayashi, S.4
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33646441100
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note
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A typical procedure of the reaction: To a solution of 1 (0.98 mg, 4.8 μmol) in a phosphate buffer (200 μL, 10 mM, pH 7.7) was added chitinase from Bacillus sp. (0.10 mg) at 30°C. The mixture was kept standing at 30°C for 24h, then the enzyme was thermally inactivated at 90°C for 5 min. The mixture was analyzed by size exclusion chromatography (SEC) with Shodex SUGAR KS-802 column eluting with distilled water at 80°C.
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0036232796
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C. Sasaki, A. Yokoyama, Y. Itoh, M. Hashimoto, T. Watanabe, T. Fukamizo, J. Biochem. 2002, 131, 557.
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(2002)
J. Biochem.
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Sasaki, C.1
Yokoyama, A.2
Itoh, Y.3
Hashimoto, M.4
Watanabe, T.5
Fukamizo, T.6
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17
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33646460688
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Ph. D. Dissertation, Tohoku University, Chap. 2
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Yields of the oligosaccharides: total 35% (dimer 24%, trimer 10%, and tetramer 1%). See also: T. Kiyosada, Ph. D. Dissertation, Tohoku University (1998), Chap. 2.
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(1998)
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Kiyosada, T.1
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33646452515
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note
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A typical procedure of the reaction: To a solution of 2 (4.09 mg, 10 μmol) in a phosphate buffer (200 μL, 10 mM, pH 9.0) was added chitinase from Bacillus sp. (0.20 mg) at 40°C. The mixture was kept standing at 40°C for 4 h followed by thermal inactivation of the enzyme at 90°C for 5 min. A white precipitate was separated by centrifugation as a water-insoluble part of 5 (2.21 mg, 54%), and the supernatant was analyzed by HPLC to determine the yield of a water-soluble part of 5 (27%).
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19
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33646465631
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note
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n = 5900 and 11800). MALDI-TOF/MS analysis showed 5 connected up to 10 saccharide units.
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