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A report of the synthesis of a 3′-N-Boc spiro[indoline-3,3′-piperidine] system via an intramolecular Heck reaction has appeared in the patent literature, see: Cassayre, J.; Molleyres, L.-P.; Maienfisch, P.; Cederbaum, F. WO 2005061512.
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A report of the synthesis of a 3′-N-Boc spiro[indoline-3,3′-piperidine] system via an intramolecular Heck reaction has appeared in the patent literature, see: Cassayre, J.; Molleyres, L.-P.; Maienfisch, P.; Cederbaum, F. WO 2005061512.
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13
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0037393778
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For a review of palladium-catalyzed α-arylation reactions of enolates, see:
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For a review of palladium-catalyzed α-arylation reactions of enolates, see:. Clukin D.A., and Hartwig J.F. Acc. Chem. Res. 36 (2003) 234-245
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For recent progress on the palladium-catalyzed intermolecular α-arylation of zinc amide enolates, see:
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For recent progress on the palladium-catalyzed intermolecular α-arylation of zinc amide enolates, see:. Hama T., Culkin D.A., and Hartwig J.F. J. Am. Chem. Soc. 128 (2006) 4976-4985
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44649160230
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note
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+): m/z 189.1 (M+H). These data were consistent with previously reported derivatives of the 1,1′-H-spiro[indoline-3,3′-piperidine] ring system, see Ref. 8.
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