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1
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3
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73449099486
-
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2-symmetric due to the same identity of the C7,C7′-positions.
-
2-symmetric due to the same identity of the C7,C7′-positions.
-
-
-
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4
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0003162048
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Chen, W. S.; Chen, Y. T.; Wang, X. Y.; Friedrichs, E.; Puff, H.; Breitmaier, E. Liebigs Ann. Chem. 1981, 1880-1885.
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hypocrellin A is called shiraiachrome B here
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0025837951
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shiraiachrome A is called hypocrellin B here
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7
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73449127104
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SciFinder indexes hypocrellin and hypocrellin A as the identical compound
-
SciFinder indexes hypocrellin and hypocrellin A as the identical compound.
-
-
-
-
8
-
-
0035768154
-
-
Which corrects: For the correct structural assignment of shiraiachrome A, see: a
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For a simple synthetic approach to allylated aromatics via the Suzuki-Miyaura cross-coupling reaction, see: Kotha, S, Behera, M, Shah, V. Synlett 2005, 1877-1880
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For a simple synthetic approach to allylated aromatics via the Suzuki-Miyaura cross-coupling reaction, see: Kotha, S.; Behera, M.; Shah, V. Synlett 2005, 1877-1880.
-
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35
-
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73449143706
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See ref 9a for another report of a dihydroperylenequinone
-
See ref 9a for another report of a dihydroperylenequinone.
-
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36
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0001353830
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2 as a catalyst for deacetalization, see: Lipshutz, B. H.; Pollart, D.; Monforte, J.; Kotsuki, H. Tetrahedron Lett. 1985, 26, 705-708.
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37
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Protic acid protocol: Horper, W.; Marner, F.-J. Phytochemistry 1996, 41, 451.
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38
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Copper/quinoline protocol: Cohen, T.; Schambach, R. A. J. Am. Chem. Soc. 1970, 92, 3189.
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Copper/quinoline protocol: Cohen, T.; Schambach, R. A. J. Am. Chem. Soc. 1970, 92, 3189.
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73449124297
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See theexperimental description in the second paper of this series (DOI: 10.1021/jo901384h).
-
See theexperimental description in the second paper of this series (DOI: 10.1021/jo901384h).
-
-
-
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