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33748909726
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M. X Hewlett, M. X Begley, W. A. Groenewegen, S. Heptinstall, D. W. Knight, J. May, U. Salan, D. Toplis, J. Chem. Soc. Perkin Trans. 1 1996, 16, 1979-1986 and references cited therein.
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12
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0000011138
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Iso-seco-tanapartholide was assigned structure 1, see
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a) Iso-seco-tanapartholide was assigned structure 1, see: S. Huneck, C. Zdero, F. Bohlmann, Phytochemistry 1986, 25, 883-889;
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13
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0027140368
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D20(iso-seco-tanapartholide) = +3.3 (c = 6.1, solvent not mentioned)}
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D20(iso-seco-tanapartholide) = +3.3 (c = 6.1, solvent not mentioned)};
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0037757214
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0000962556
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18
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72849140033
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See Supporting Information for further details
-
See Supporting Information for further details.
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-
-
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19
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72849140570
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It was also confirmed that the active fraction did not target the reporter protein, firefly luciferase, by using an in vitro assay (data not shown)
-
It was also confirmed that the active fraction did not target the reporter protein, firefly luciferase, by using an in vitro assay (data not shown).
-
-
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20
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54949145019
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72849133410
-
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[8] contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
[8] contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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25
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0003587845
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P. A. Grieco, M. Meyers, R. S. Finkelhor, J. Org. Chem. 1974, 39, 119-120.
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26
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84971046730
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-
It cannot be ruled out that lead tetraacetate rapidly cleaves 7 and 25 without forming a cyclic ester intermediate and that the speed of the reaction results from release of steric congestion on. cleavage of the Cl-C10 bond. We thank a reviewer for raising this possibility
-
R. Criegee, E. Hoger, G. Huber, P. Kruck, F. Marktscheffel, H. Schellenberger, Justus Liebigs Ann. Chem. 1956, 599, 81-125. It cannot be ruled out that lead tetraacetate rapidly cleaves 7 and 25 without forming a cyclic ester intermediate and that the speed of the reaction results from release of steric congestion on. cleavage of the Cl-C10 bond. We thank a reviewer for raising this possibility.
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Criegee, R.1
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Schellenberger, H.6
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27
-
-
72849141994
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-
In this reaction a compound tentatively assigned as the C3 oxo derivative of I. was formed
-
In this reaction a compound tentatively assigned as the C3 oxo derivative of I. was formed.
-
-
-
-
28
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72849129860
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-
3)
-
3).
-
-
-
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29
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72849153064
-
-
This sample was kindly provided by Professor Todorova. For example, and references cited therein
-
This sample was kindly provided by Professor Todorova. For example, see M. Todorova, E. Mustakerova, E. Tsankova, Dokl. Bulg. Akad. Nauk. 2005, 58, 25-32 and references cited therein.
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Todorova, M.1
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30
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4344592673
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For previous reports on the biological activity of this family of natural products, see: a
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For previous reports on the biological activity of this family of natural products, see: a) H. Z. Jin, J. H. Lee, D. Lee, Y. S. Hong, Y. H. Kim, J. J. Lee, Phytochemistry 2004, 65, 2247-2253;
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31
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