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For references to the biological activity of compounds containing the 3-hydroxyl indoline substructure, see:
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For references to the biological activity of compounds containing the 3-hydroxyl indoline substructure, see:. Engel S., Skoumbourdis A.P., Childress J., Neumann S., Deschamps J.R., Thomas C.J., Colson A.-O., Costanzi S.G., and Marvin C. J. Am. Chem. Soc. 130 (2008) 5115
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For recent reviews and selected examples on indole/indoline synthesis, see:
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NAr reaction; see:
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NAr reaction; see:. Kogan K., and Biali S.E. Org. Lett. 9 (2007) 2393
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Katz, J.L.6
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26
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60249093154
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NAr on a pentafluorinated benzene derivative, see: 385 and 622
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NAr on a pentafluorinated benzene derivative, see:. Petrov V.P., and Barkhash V.A. Khim Geterotsikl Soedin 73 (1970) 385 and 622
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34248577036
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For epoxide opening with amines to form amino alcohols; see: and references cited therein
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For epoxide opening with amines to form amino alcohols; see:. Shivani, Pujala B., and Chakraborti A.K. J. Org. Chem. 72 (2007) 3713 and references cited therein
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Shivani1
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31
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44449161081
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For N-cyclopropylation of indoles; see:
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For N-cyclopropylation of indoles; see:. Tsuritani T., Strotman N.A., Yamamoto Y., Kawasaki M., Yasuda N., and Mase T. Org. Lett. 10 (2008) 1653
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Mase, T.6
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33846093068
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Gagnon A., St-Onge M., Little K., Duplessis M., and Barabe F. J. Am. Chem. Soc. 129 (2007) 44
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Gagnon, A.1
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Barabe, F.5
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60249094490
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note
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NAr reaction in neat n-butyl amine at 150 °C for 12 h.
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36
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60249095502
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note
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3, 470.5 MHz): δ -139.07.
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