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1
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0022374460
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Otake N., Takatsu T., Nakayama H., Shimazu A., Furihata K., Ikeda K., Furihata K., Seto H., J. Antibiot., 38, 1806-1809 (1985).
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Otake, N.1
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Furihata, K.5
Ikeda, K.6
Furihata, K.7
Seto, H.8
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2
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0022407321
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Otake N., Abe Y., Nakayama H., Shimazu A., Furihata K., Ikeda K., Furihata K., Seto H., J. Antibiot., 38, 1810-1812 (1985).
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Otake, N.1
Abe, Y.2
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Ikeda, K.6
Furihata, K.7
Seto, H.8
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3
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0022406199
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Achenbach H., Muhlenfeld A., Fauth U., Zahner H., Tetrahedron Lett., 26, 6167-6170 (1985).
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Achenbach, H.1
Muhlenfeld, A.2
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Zahner, H.4
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4
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0023005646
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Achenbach H., Muhlenfeld A., Fauth U., Zahner H., J. Antibiot., 39, 1760-1764 (1986).
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5
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Mandala S. M., Thornton R. A., Milligan J., Rosenbach M., Garcia-Calvo M., Bull H. G., Harris G., Abruzzo G. K., Flattery A. M., Gill C. J., Bartizal K., Dreikorn S., Kurtz M. B., J. Biol. Chem., 273, 14942-14949 (1998).
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Bull, H.G.6
Harris, G.7
Abruzzo, G.K.8
Flattery, A.M.9
Gill, C.J.10
Bartizal, K.11
Dreikorn, S.12
Kurtz, M.B.13
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6
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14444272050
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Harris G. H., Shafiee A., Cabello M. A., Curotto J. E., Genilloud O., Goklen K. E., Kurtz M. B., Rosenbach M., Salmon P. M., Thornton R. A., Zink D. L., Mandala S. M., J. Antibiot., 51, 837-844 (1998).
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Harris, G.H.1
Shafiee, A.2
Cabello, M.A.3
Curotto, J.E.4
Genilloud, O.5
Goklen, K.E.6
Kurtz, M.B.7
Rosenbach, M.8
Salmon, P.M.9
Thornton, R.A.10
Zink, D.L.11
Mandala, S.M.12
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8
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0034622920
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Sugimoto Y., Imamura H., Shimizu A., Nakano M., Nakajima S., Abe S., Yamada K., Morishima H., Tetrahedron: Asymmetry, 11, 3609-3617 (2000). Lipase LIP® was purchased from TOYOBO.
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Sugimoto, Y.1
Imamura, H.2
Shimizu, A.3
Nakano, M.4
Nakajima, S.5
Abe, S.6
Yamada, K.7
Morishima, H.8
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9
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28044432249
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note
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The configuration of (S)-8 was determined by conversion to a chiral compound, (S)-(2)-1-phenyl-1-propanol by following procedure, then its specific rotation was compared with that of commercially available sample which was purchased from Aldrich. Chemical Presented.
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10
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0029084414
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Williams J. M., Jobson R. B., Yasuda N., Marchesini G., Dolling Ulf-H., Grabowski E. J. J., Tetrahedron Lett., 36, 5461-5464 (1995).
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, pp. 5461-5464
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Williams, J.M.1
Jobson, R.B.2
Yasuda, N.3
Marchesini, G.4
Dolling, U.-H.5
Grabowski, E.J.J.6
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12
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84987557280
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Seebach D., Aebi J. D., Gandner-Coquoz M., Naef R., Helv. Chim. Acta, 70, 1194-1216 (1987). As regards this reaction, Tse proposed the chelation model of lithiated 5 in ref. 4. Excellent stereoselectivity was observed by preferentially nucleophilic attack from the less hindered convex side. Chemical Presented.
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(1987)
Helv. Chim. Acta
, vol.70
, pp. 1194-1216
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Seebach, D.1
Aebi, J.D.2
Gandner-Coquoz, M.3
Naef, R.4
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13
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28044447548
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note
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+).
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14
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0006427132
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Braum N. A., Klein I., Spitzner D., Vogler B., Braum S., Borrmann H., Simon A., Liebigs. Ann., 1995, 2165-2169 (1995).
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Braum, N.A.1
Klein, I.2
Spitzner, D.3
Vogler, B.4
Braum, S.5
Borrmann, H.6
Simon, A.7
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15
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28044466573
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note
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+).
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16
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28044470884
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note
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3 conidia/ml. Test samples were dissolved and serially twofold diluted in dimethyl sulfoxide. Aliquots of 2 μl were distributed to a 96-well, flat-bottomed plate, then plates were filled with 200 μl of cell or conidia solution. The MIC was de-fined as the lowest concentration of samples that completely prevented visible growth was inhibited.
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