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12
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77949849350
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THBC 6 was obtained in four steps from L-tryptophane (50% yield). For more details, see the Supporting Information
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THBC 6 was obtained in four steps from L-tryptophane (50% yield). For more details, see the Supporting Information.
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-
-
-
13
-
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3142592480
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For a general review on haloindolenines, see
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For a general review on haloindolenines, see: (a) Ikeda, M.; Tamura, Y. Hetrocycles 1980, 14, 867-888.
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Ikeda, M.1
Tamura, Y.2
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14
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36348942481
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For an example of the use of choroindolenine in synthesis
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(b) For an example of the use of choroindolenine in synthesis, see: Miyazaki, T.; Yokoshima, S.; Simizu, S.; Osada, H.; Tokuyama, H.; Fukuyama, T. Org. Lett. 2007, 9, 4737-4740.
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Tokuyama, H.5
Fukuyama, T.6
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15
-
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38849204313
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-
For a similar rearrangement, references cited therein
-
For a similar rearrangement, see: Pouillhès, A.; Kouklovsky, C.; Langlois, Y.; Baltaze, J. P.; Vispe, S.; Annereau, J. P.; Barett, J. M. Bioorg. Med. Chem. Lett. 2008, 18, 1212-1216, and references cited therein.
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Kouklovsky, C.2
Langlois, Y.3
Baltaze, J.P.4
Vispe, S.5
Annereau, J.P.6
Barett, J.M.7
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16
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0019200032
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Andriamialisoa, R. Z.; Langlois, N.; Langlois, Y.; Potier, P. Tetrahedron 1980, 36, 3053-3060.
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Tetrahedron
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Langlois, N.2
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Potier, P.4
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17
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53849119193
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(a) Colombo, F.; Cravotto, G.; Palmisano, G.; Penoni, A.; Sisti, M. Eur. J. Org. Chem. 2008, 2801-2807.
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Colombo, F.1
Cravotto, G.2
Palmisano, G.3
Penoni, A.4
Sisti, M.5
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19
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33947596218
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(c)De la Herrán, G.; Segura, A.; Csákÿ, A. G. Org. Lett. 2007, 9, 961-964.
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De La Herrán, G.1
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Csákÿ, A.G.3
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42749089147
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(d)Matsuo, J.; Tanaki, Y.; Ishibashi, H. Tetrahedron 2008, 64, 5262-5267.
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Matsuo, J.1
Tanaki, Y.2
Ishibashi, H.3
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21
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20444507249
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For a similar intermediate
-
(e) For a similar intermediate, see also: Nicolaou, K. C.; Lee, S.; Estrada, A. A.; Zak, M. Angew. Chem. Int. Ed. 2005, 44, 3736-3740.
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Nicolaou, K.C.1
Lee, S.2
Estrada, A.A.3
Zak, M.4
-
22
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0024810762
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-
For a similar rearrangement
-
For a similar rearrangement, see: Irikawa, H.; Mutoh, S.; Uehara, M.; Okumura, Y. Bull, Chem. Soc. Jpn. 1989, 62, 3031-3033.
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Irikawa, H.1
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Okumura, Y.4
-
23
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-
0041568539
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-
Compound 13 should come from the hydrolysis of an imminium, mesomeric form of 10. For a similar example
-
Compound 13 should come from the hydrolysis of an imminium, mesomeric form of 10. For a similar example, see: Pouilhès, A.; Langlois, Y.; Chiaroni, A. Synlett 2003, 10, 1488-1490.
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Synlett
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Pouilhès, A.1
Langlois, Y.2
Chiaroni, A.3
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