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T. Sakai, I. Kawabata, T. Kishimoto, T. Ema, and M. Utaka, J. Org. Chem., 62, 4906 (1997).
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Sakai, T.1
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2
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0032558671
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T. Sakai, T. Kishimoto, Y. Tanaka, T. Ema, and M. Utaka, Tetrahedron Lett., 39, 7881 (1998).
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Sakai, T.1
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3
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0141449817
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note
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The temperature effect is an inherent phenomenon in the reactions of both primary and secondary alcohols. However, the secondary alcohols remarkably decrease the reaction rate at the low temperatures. Therefore, in a viewpoint of practical utilization, this method is useful for primary alcohols, which still have acceptable rate even at the low temperatures.
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4
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0036340599
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Review for azirines: F. Palacios, A. M. Ochoa de Retana, E. Martines de Marigorta, and J. Manuel de los Santos, Org. Prep. Proced. Int., 34, 219 (2002).
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Org. Prep. Proced. Int.
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Palacios, F.1
De Retana, A.M.O.2
De Marigorta, E.M.3
De los Santos, J.M.4
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5
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0347598189
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Review: E. Ljubović, M. Majeric-Elenkov, A. Avdagić, and V. Šunjić, Food Technol. Biotechnol., 37, 215 (1999).
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Food Technol. Biotechnol.
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Ljubović, E.1
Majeric-Elenkov, M.2
Avdagić, A.3
Šunjić, V.4
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7
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0003458664
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ed by K. Drauz and H. Waldmann, Wiley-VCH, Weinheim
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b) "Enzyme Catalysis in Organic Synthesis," ed by K. Drauz and H. Waldmann, Wiley-VCH, Weinheim (2002).
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Enzyme Catalysis in Organic Synthesis
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8
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20644469267
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C.-S. Chen, Y. Fujimoto, G. Girdaukas, and J. C. Sih, J. Am. Chem. Soc., 104, 7294 (1982).
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, vol.104
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Chen, C.-S.1
Fujimoto, Y.2
Girdaukas, G.3
Sih, J.C.4
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9
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0141784707
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note
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Total turnover number (TTN) is the term defined as the number of mole of product formed per mole of enzyme during the course of a complete reaction. Here, TTN/h shows the total tumover number per hour.
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10
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0029969716
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a) T. Ema, S. Maeno, Y. Takaya, T. Sakai, and M. Utaka, J. Org. Chem., 61, 8610 (1996).
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Ema, T.1
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0029915768
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b) T. Ema, S. Maeno, Y. Takaya, T. Sakai, and M. Utaka, Tetrahedron: Asymmetry, 7, 625 (1996).
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Tetrahedron: Asymmetry
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Ema, T.1
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12
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0035911442
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M. Kawasaki, M. Goto, S. Kawabata, and T. Kometani, Tetrahedron: Asymmetry, 12, 585 (2001).
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Kawasaki, M.1
Goto, M.2
Kawabata, S.3
Kometani, T.4
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13
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0033538636
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Recent reports for the enzymatic resolution with various acylating reagents: a) M. Kawasaki, M. Goto, S. Kawabata, T. Kodama, and T. Kometani, Tetrahedron Lett., 40, 5223 (1999).
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Tetrahedron Lett.
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Kawasaki, M.1
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Kometani, T.5
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14
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0343130518
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b) K. Hirose, H. Naka, M. Yano, S. Ohashi, K. Naemura, and Y. Tobe, Tetrahedron: Asymmetry, 11, 1199 (2000).
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Tetrahedron: Asymmetry
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Hirose, K.1
Naka, H.2
Yano, M.3
Ohashi, S.4
Naemura, K.5
Tobe, Y.6
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15
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0033972206
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c) Y. Kita, Y. Takebe, K. Murata, T. Naka, and S. Akai, J. Org. Chem., 65, 83 (2000).
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J. Org. Chem.
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Kita, Y.1
Takebe, Y.2
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Naka, T.4
Akai, S.5
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18
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0037169063
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f) S. Akai, T. Naka, T. Fujita, Y. Takebe, T. Tsujino, and Y. Kita, J. Org. Chem., 67, 411 (2002).
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J. Org. Chem.
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Akai, S.1
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19
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0034697232
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a) M. Kamori, T. Hori, Y. Yamashita, Y. Hirose, and Y. Naoshima, J. Mol. Catal. B: Enzym., 9, 269 (2000).
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J. Mol. Catal. B: Enzym.
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Kamori, M.1
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Naoshima, Y.5
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20
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0034281828
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b) K. Kato, Y. Gong, T. Saito, and H. Kimoto, J. Biosci. Bioeng., 90, 332 (2000).
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J. Biosci. Bioeng.
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Kato, K.1
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Kimoto, H.4
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21
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0034608029
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c) T. Sakai, Y. Miki, M. Tsuboi, H. Takeuchi, T. Ema, K. Uneyama, and M. Utaka, J. Org. Chem., 65, 2740 (2000).
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J. Org. Chem.
, vol.65
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Sakai, T.1
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Ema, T.5
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Utaka, M.7
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22
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0035806158
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d) M. Suzuki, C. Nagasawa, and T. Sugai, Tetrahedron, 57, 4841 (2001).
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Tetrahedron
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Suzuki, M.1
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23
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0042662635
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T. Sakai, K. Hayashi, F. Yano, M. Takami, M. Ino, T. Korenaga, and T. Ema, Bull. Chem. Soc. Jpn., 76, 1441 (2003).
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Bull. Chem. Soc. Jpn.
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, pp. 1441
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Sakai, T.1
Hayashi, K.2
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Takami, M.4
Ino, M.5
Korenaga, T.6
Ema, T.7
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24
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0141784706
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note
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Toyonite D-M has 120 nm of mean pore size and Toyonite 200M has 60 nm mean pore size. Both of them have 3-(2-meth-acryloyloxy)propylsilanetrioxyl bridges on the surface. They are commercially available from Toyo Denka Kogyo Co. Ltd. Toyonite-immobilized lipase is also available from Amano Enzyme Inc. or Wako Pure Chemical Industries, Ltd. as Lipase PS-C "Amano" II.
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25
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0037025268
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J. M. Palomo, G. F.-Lorente, C. Mateo, M. Fuentes, R. F.-Lafuente, and J. M. Guisan, Tetrahedron: Asymmetry, 13, 1337 (2002).
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Tetrahedron: Asymmetry
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Palomo, J.M.1
Lorente, G.F.2
Mateo, C.3
Fuentes, M.4
Lafuente, R.F.5
Guisan, J.M.6
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