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Murata, M.1
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6
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Kita M., Ohishi N., Konishi K., Kondo M., Koyama T., Kitamura M., Yamada K., and Uemura D. Tetrahedron 63 (2007) 6241-6251
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Kita, M.1
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Kitamura, M.6
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Uemura, D.8
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7
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67949096901
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Symbiodinolide (1) is a structural congener of zooxanthellatoxins which are polyol macrolides isolated from the dinoflagellate Symbiodinium sp. For the structural elucidation of zooxanthellatoxins, see:
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Symbiodinolide (1) is a structural congener of zooxanthellatoxins which are polyol macrolides isolated from the dinoflagellate Symbiodinium sp. For the structural elucidation of zooxanthellatoxins, see:
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8
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33751386629
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11
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0029156787
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Nakamura H., Asari T., Fujimaki K., Maruyama K., Murai A., Ohizumi Y., and Kan Y. Tetrahedron Lett. 36 (1995) 7255-7258
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16
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Takamura, H.1
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Kadota, I.5
Uemura, D.6
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17
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58149339546
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Takamura H., Kadonaga Y., Yamano Y., Han C., Aoyama Y., Kadota I., and Uemura D. Tetrahedron Lett. 50 (2009) 863-866
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Takamura, H.1
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Kadota, I.6
Uemura, D.7
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18
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67649625261
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Murata T., Sano M., Takamura H., Kadota I., and Uemura D. J. Org. Chem. 74 (2009) 4797-4803
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Murata, T.1
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19
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67949103049
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note
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For a preliminary communication, see Ref. 5b.
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21
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28444451575
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Niggemann J., Bedorf N., Flörke U., Steinmetz H., Gerth K., Reichenbach H., and Höfle G. Eur. J. Org. Chem. (2005) 5013-5018
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Niggemann, J.1
Bedorf, N.2
Flörke, U.3
Steinmetz, H.4
Gerth, K.5
Reichenbach, H.6
Höfle, G.7
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22
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34447299920
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Williams P.G., Miller E.D., Asolkar R.N., Jensen P.R., and Fenical W. J. Org. Chem. 72 (2007) 5025-5034
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Williams, P.G.1
Miller, E.D.2
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Jensen, P.R.4
Fenical, W.5
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23
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58149203501
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Oishi T., Kanemoto M., Swasono R., Matsumori N., and Murata M. Org. Lett. 10 (2008) 5203-5206
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Oishi, T.1
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Murata, M.5
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25
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67949084578
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note
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Structural determination of other degraded products obtained by cross-metathesis will be reported in the near future.
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27
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18744369934
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For determination of the absolute stereochemistry of secondary/secondary diols by the modified Mosher method, see:
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For determination of the absolute stereochemistry of secondary/secondary diols by the modified Mosher method, see:. Freire F., Seco J.M., Quiñoá E., and Riguera R. J. Org. Chem. 70 (2005) 3778-3790
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Freire, F.1
Seco, J.M.2
Quiñoá, E.3
Riguera, R.4
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30
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67949083047
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note
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The absolute configuration of 6 was unambiguously confirmed by the modified Mosher method.
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36
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67949089188
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note
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The absolute stereochemistry at the resulting chiral center of 11 was determined by the modified Mosher method.
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42
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33845282438
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Corey E.J., Bakshi R.K., Shibata S., Chen C.-P., and Singh V.K. J. Am. Chem. Soc. 109 (1987) 7925-7926
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Singh, V.K.5
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