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33644967024
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note
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+ expect. 557.2, obsd 557.2). Synthesis of authentic standards (diastereomeric mixtures) and evaluation of chemical reaction rates was performed by reacting amine and aldehyde substrates (20 mM concentration) under aqueous conditions (150 mM maleic acid, pH 2).
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18
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0037424703
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Compounds 11 and 13 were synthesized from the corresponding commercially available indole-3-carbaldehydes as previously reported. (Harada, H.; Hirokawa, Y.; Suzuki, K.; Hiyama, Y.; Oue, M.; Kawashima, H.; Yoshida, N.; Furutani, Y.; Kato, S. Bioorg. Med. Chem. Lett. 2003, 13, 1301.)
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Kato, S.9
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19
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78650216698
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USA
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Substrates 10 and 7 were synthesized from the corresponding commercially available indoles as previously described. (Chen, Z.; Cohen, M. P.; Fisher, M. J.; Giethlen, B.; Gillig, J. R.; McCowan, J. R.; Miller, S. C.; Schaus, J. M. Preparation of N-(2-arylethyl)benzylamines as antagonists of the 5-HT6 receptor.: USA, 2002; p 216.)
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20
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84987306375
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Benzofuran (4) and benzothiophene (5) derivatives were generated from reduction of the commercially available nitrile compounds. (Shafiee, A.; Mohamadpour, M. J. Heterocycl. Chem. 1978, 15, 481.)
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0342634592
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The pyrrole ethanamine compound (16) was synthesized as described. (Wasley, J. W. F.; Hamdan, A. Synth. Commun. 1985, 15, 71.) All other tryptamine analogs were commercially available.
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3142579793
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84982076728
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3OH, 7:3) to yield purified secologanin (1 g). NMR and mass spectral data matched previously reported values
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Kinast, G.1
Tietze, L.F.2
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12844283942
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L. Barleben, X. Ma, J. Koepke, G. Peng, H. Michel, and J. Stoeckigt Biochim. Biophys. Acta 1747 2005 89
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1542510893
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30
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33644988101
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note
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+ expect. 365.4, obsd 365.5).
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