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In this case, the Pd-catalyzed amination proceeds intramolecularly: (f) Thansandote, P.; Raemy, M.; Rudolph, A.; Lautens, M. Org. Lett. 2007, 9, 5255.
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For evidence of intramolecular Cu-catalyzed hydroamidation of an unsaturated moiety, see ref 11b
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For evidence of intramolecular Cu-catalyzed hydroamidation of an unsaturated moiety, see ref 11b.
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For recent examples of the synthesis of enantiomerically enriched indolines, see
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(a) For recent examples of the synthesis of enantiomerically enriched indolines, see: Arp, F. O.; Fu, G. C. J. Am. Chem. Soc. 2006, 128, 14265.
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For examples of trans-1,2,3,4,4a,9a-hexahydrocarbazoles, see: (a) Smolinsky, G. J. Am. Chem. Soc. 1961, 83, 2489.
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