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1
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33745752460
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(a) Baur, S.; Niehaus, J.; Karagouni, A. D.; Katsifas, E. A.; Chalkou, K.; Meintanis, C.; Jones, A. L.; Goodfellow, M.; Ward, A. C.; Beil, W.; Schneider, K.; Sussmuth, R. D.; Fiedler, H.-P. J. Antibiot. 2006, 59, 293.
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Baur, S.1
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Chalkou, K.5
Meintanis, C.6
Jones, A.L.7
Goodfellow, M.8
Ward, A.C.9
Beil, W.10
Schneider, K.11
Sussmuth, R.D.12
Fiedler, H.-P.13
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2
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33645774139
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(b) Schneider, K.; Nicholson, G.; Strobele, M.; Baur, S.; Niehaus, J.; Fiedler, H.-P.; Sussmuth, R. D. J. Antibiot. 2006, 59, 105.
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Sussmuth, R.D.7
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3
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0031817695
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For studies on fluostatin A and B, see: a
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For studies on fluostatin A and B, see: (a) Akiyama, T.; Nakamura, K. T.; Takahashi, Y.; Naganawa, H.; Muraoka, Y.; Aoyagi, T.; Takeuchi, T. J. Antibiot. 1998, 51, 586.
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Akiyama, T.1
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Naganawa, H.4
Muraoka, Y.5
Aoyagi, T.6
Takeuchi, T.7
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4
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0031848569
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(b) Akiyama, T.; Harada, S.; Kojima, F.; Takahashi, Y.; Imada, C.; Okami, Y.; Muraoka, Y.; Yakeuchi, T. J. Antibiot. 1998, 51, 553.
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Akiyama, T.1
Harada, S.2
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Takahashi, Y.4
Imada, C.5
Okami, Y.6
Muraoka, Y.7
Yakeuchi, T.8
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5
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0014801863
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(a) Ito, S.; Matsuya, T.; Omura, S.; Otani, M.; Nakagawa, A.; Takeshima, H.; Iwai, Y.; Ohtani, M.; Hata, T. J. Antibiot. 1970, 23, 315.
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Ito, S.1
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Omura, S.3
Otani, M.4
Nakagawa, A.5
Takeshima, H.6
Iwai, Y.7
Ohtani, M.8
Hata, T.9
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6
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0015081375
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(b) Hata, T.; Omura, S.; Iwai, Y.; Nakagawa, A.; Otani, M. J. Antibiot. 1971, 24, 353.
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Hata, T.1
Omura, S.2
Iwai, Y.3
Nakagawa, A.4
Otani, M.5
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7
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0028050438
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(c) Gould, S. J.; Tamayo, N.; Melville, C. R.; Cone, M. C. J. Am. Chem. Soc. 1994, 116, 2207.
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Gould, S.J.1
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Melville, C.R.3
Cone, M.C.4
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8
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0027997344
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(d) Mithani, S.; Weeratunga, G.; Taylor, N. J.; Dmitrienko, G. I. J. Am. Chem. Soc. 1994, 116, 2209.
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Mithani, S.1
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9
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0034734361
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For a proposed biochemical interconversion between kinamycins and fluostatins, see
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For a proposed biochemical interconversion between kinamycins and fluostatins, see: Proteau, P. J.; Li, Y.; Chen, J.; Williamson, R. T.; Gould, S. J.; Laufer, R. S.; Dmitrienko, G. I. J. Am. Chem. Soc. 2000, 122, 8325.
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Proteau, P.J.1
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Chen, J.3
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Dmitrienko, G.I.7
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11
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34249040542
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(b) Quin, L. D.; Hughes, A. N.; Lawson, H. F.; Good, A. L. Tetrahedron 1983, 39, 401.
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Quin, L.D.1
Hughes, A.N.2
Lawson, H.F.3
Good, A.L.4
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12
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40949101998
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-
For the preparation and full characterization of compound 6, see Supporting Information.
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For the preparation and full characterization of compound 6, see Supporting Information.
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-
-
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13
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0343519580
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(a) Carreno, M. C.; Farina, F.; Galan, A.; Ruano, J. L. G. J. Chem. Res. 1979, 296.
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Carreno, M.C.1
Farina, F.2
Galan, A.3
Ruano, J.L.G.4
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14
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0007183627
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(b) Carreno, M. C.; Farina, F.; Galan, A.; Ruano, J. L. G. J. Chem. Res. 1981, 370.
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15
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0007248132
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(c) Jarvo, E. R.; Boothroyd, S. R.; Kerr, M. A. Synlett 1996, 9, 897.
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Jarvo, E.R.1
Boothroyd, S.R.2
Kerr, M.A.3
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16
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0002679613
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(d) Gerstenberger, I.; Hansen, M.; Mauvais, A.; Warichow, R.; Winterfeldt, E. Eur. J. Org. Chem. 1998, 63, 643.
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Gerstenberger, I.1
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Winterfeldt, E.5
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17
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84989546359
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(a) Mikami, K. M.; Terada, M.; Narisawa, S.; Nakai, T. Synlett 1992, 255.
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Synlett
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Mikami, K.M.1
Terada, M.2
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Nakai, T.4
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18
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0000210159
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(b) Mikami, K. M.; Motoyama, Y.; Terada, M. J. Am. Chem. Soc. 1994, 116, 2812.
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20
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37049083606
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Compounds 7 and 8 were prepared by sequential oxidation of the corresponding phenols with iodobenzene diacetate in MeOH. Pelter, A.; Elgendy, S. M. A. J. Chem. Soc., Perkin Trans. 1 1993, 1891.
-
Compounds 7 and 8 were prepared by sequential oxidation of the corresponding phenols with iodobenzene diacetate in MeOH. Pelter, A.; Elgendy, S. M. A. J. Chem. Soc., Perkin Trans. 1 1993, 1891.
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-
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21
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0026795362
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This was followed by BF3·OEt2-catalyzed transacetalization with ethylene glycol. Pirrung, M. C, Nunn, D. S. Tetrahedron Lett. 1992, 33, 6591. The experimental details are described in Supporting Information
-
2-catalyzed transacetalization with ethylene glycol. Pirrung, M. C.; Nunn, D. S. Tetrahedron Lett. 1992, 33, 6591. The experimental details are described in Supporting Information.
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-
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23
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40949090781
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In the absence of the epimerization, isomerizalion of the nonenone double bond to the tetrasubstituted position occurred in the epoxidation stage
-
In the absence of the epimerization, isomerizalion of the nonenone double bond to the tetrasubstituted position occurred in the epoxidation stage.
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-
-
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24
-
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0027507601
-
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4a in compounds 19a,b is not assigned.
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4a in compounds 19a,b is not assigned.
-
-
-
-
25
-
-
49549130554
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-
6a in compounds 20a,b and 21a,b is not assigned.
-
6a in compounds 20a,b and 21a,b is not assigned.
-
-
-
-
27
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0035820165
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