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U.S. Patent 5,214,037, 1993
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(a) Kubota, T.; Kume, M. U.S. Patent 5,214,037, 1993.
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Kubota, T.1
Kume, M.2
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3
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0027473861
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(b) Kume, M.; Kubota, T.; Kimura, Y.; Nakashimizu, H.; Motokawa, K.; Nakano, M. J. Antibiotics 1993, 46, 177-192.
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Nakashimizu, H.4
Motokawa, K.5
Nakano, M.6
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4
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0027509628
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(c) Kume, M.; Kubota, T.; Kimura, Y.; Nakashimizu, H.; Motokawa, K. J. Antibiotics 1993, 46, 316-330.
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Kume, M.1
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Nakashimizu, H.4
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Motokawa, K.5
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6
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0037923948
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U.S. Patent 5,407,929, 1995
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(a) Takahashi, H.; Ide, Y. U.S. Patent 5,407,929, 1995.
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Takahashi, H.1
Ide, Y.2
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8
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0038600235
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Patent Application No. JP 1968-90647 (JP Patent 13106, 1973)
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(a) Ashida, K.; Koyama, S.; Sawada, T.; Ishimatsu, T. Patent Application No. JP 1968-90647 (JP Patent 13106, 1973).
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Ashida, K.1
Koyama, S.2
Sawada, T.3
Ishimatsu, T.4
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9
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0037586040
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Patent JP Application No. 1970-59441 (JP Patent 8068, 1975)
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(b) Kobayashi, T.; Okada, A. Patent JP Application No. 1970-59441 (JP Patent 8068, 1975).
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Kobayashi, T.1
Okada, A.2
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10
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Smutek, G.; Raveling, H. Patent Application No. DE 1982-3241070.
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Smutek, G.1
Raveling, H.2
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0037923945
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JP Patent 76463, 1993
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Inoue, Y.1
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12
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0037586038
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Patent Application No. JP 1994-193059
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A portion of this study (Methods G and H) was patented. Takahashi, H.; Masui, Y. Patent Application No. JP 1994-193059.
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Takahashi, H.1
Masui, Y.2
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15
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0037923943
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note
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Viscosity of the gelatinous slurry during the agitation under the acidic condition (1 M to 3 M HCl) was variable not only between the runs but also in the same run. The thixotropic phenomenon depended upon the concentration of acid. When the concentration of HCl was ∼0.0001 M (pH 4), no phenomenon occurred. However, a higher concentration of HCl than 1 M was necessary for crystallization.
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16
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0037923947
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note
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HPC is classified by the viscosity of its aqueous solution depending on its degree of polymerization. Viscosity of 2% aqueous solution at 20°C (CPS): HPC-L, 6-10; HPC-M, 150-400.
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17
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0004294969
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Butterworth-Heinemann: Oxford
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(a) Mullin, J. W. In Crystallization, 3rd ed.; Butterworth-Heinemann: Oxford, 1997; pp 248-257.
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Mullin, J.W.1
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18
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74049096534
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(b) Berkovitch-Yellin, Z.; Addadi, L.; Idelson, M.; Lahav, M.; Leiserowitz, L. Angew. Chem. Suppl. 1982, 1336-1345.
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(1982)
Angew. Chem. Suppl.
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Berkovitch-Yellin, Z.1
Addadi, L.2
Idelson, M.3
Lahav, M.4
Leiserowitz, L.5
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19
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0037923944
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note
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2O molecule and N1-position of triazolyl group is observed. The N3-position of the triazolyl group is used for intermolecular hydrogen bonding.
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