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1
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34848884051
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For some reviews see:
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13
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0342699622
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Guilloteau-Bertin B., Compere D., Gil L., Marazano C., and Das B.C. Eur. J. Org. Chem. (2000) 1391
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Eur. J. Org. Chem.
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Guilloteau-Bertin, B.1
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15
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27444437213
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Etxebarria J., Vicario J.L., Badia D., Carrillo L., and Ruiz N. J. Org. Chem. 70 (2005) 8790
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J. Org. Chem.
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Etxebarria, J.1
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Badia, D.3
Carrillo, L.4
Ruiz, N.5
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16
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34848875538
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For other selected synthetic approaches to enantioenriched alkylpiperidines from β-amino carbonyl derivatives, see:
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19
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22144454646
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Davis F.A., Zhang J., Li Y., Xu H., and DeBrosse C. J. Org. Chem. 70 (2005) 5413
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J. Org. Chem.
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Davis, F.A.1
Zhang, J.2
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DeBrosse, C.5
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21
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2542446198
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Burke A.J., Davies S.G., Garner A.C., McCarthy T.D., Roberts P.M., Smith A.D., Rodriguez-Solla H., and Vickers R.J. Org. Biomol. Chem. 2 (2004) 1387
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Burke, A.J.1
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Roberts, P.M.5
Smith, A.D.6
Rodriguez-Solla, H.7
Vickers, R.J.8
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22
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0346731103
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Marin J., Didierjean C., Aubry A., Casimir J.-R., Briand J.-P., and Guichard G. J. Org. Chem. 69 (2004) 130
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Marin, J.1
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28
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0000051598
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Kawakami T., Ohtake H., Arakawa H., Okachi T., Imada Y., and Murahashi S. Org. Lett. 1 (1999) 107
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Kawakami, T.1
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Murahashi, S.6
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30
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34848841948
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note
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In some cases (S)-configurated derivatives were obtained as a result of the application of CIP rules.
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31
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34848870987
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For some selected examples on the formation of piperidines via intramolecular reductive amination see:
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33
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33751351370
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Adriaenssens L.V., Austin C.A., Gibson M., Smith D., and Hartley R.C. Eur. J. Org. Chem. (2006) 4998
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Eur. J. Org. Chem.
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Adriaenssens, L.V.1
Austin, C.A.2
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Smith, D.4
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36
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4544341089
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La Ferla B., Bugada P., Cipolla L., Peri F., and Nicotra F. Eur. J. Org. Chem. (2004) 2451
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(2004)
Eur. J. Org. Chem.
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La Ferla, B.1
Bugada, P.2
Cipolla, L.3
Peri, F.4
Nicotra, F.5
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37
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0037421233
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Lee Y.-S., Shin Y.-H., Kim Y.-H., Lee K.-Y., Oh C.-Y., Pyun S.-J., Park H.-J., Jeong J.-H., and Ham W.-H. Tetrahedron: Asymmetry 14 (2003) 87
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Lee, Y.-S.1
Shin, Y.-H.2
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Oh, C.-Y.5
Pyun, S.-J.6
Park, H.-J.7
Jeong, J.-H.8
Ham, W.-H.9
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43
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0042865048
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20 +3.9 (c 1.1, EtOH) for a sample of (R)-pipecoline hydrochloride obtained by us; lit. +3.97 (c 1.0, EtOH).
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20 +3.9 (c 1.1, EtOH) for a sample of (R)-pipecoline hydrochloride obtained by us; lit. +3.97 (c 1.0, EtOH). Andres J.M., Herraiz-Sierra I., Pedrosa R., and Perez-Encabo A. Eur. J. Org. Chem. (2000) 1719
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Eur. J. Org. Chem.
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Andres, J.M.1
Herraiz-Sierra, I.2
Pedrosa, R.3
Perez-Encabo, A.4
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44
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0000683796
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20 -3.1 (c 0.2, EtOH) for the R isomer:
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20 -3.1 (c 0.2, EtOH) for the R isomer:. Katritzky A.R., Qiu G., Yang B., and Steel P.J. J. Org. Chem. 63 (1998) 6699
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(1998)
J. Org. Chem.
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Katritzky, A.R.1
Qiu, G.2
Yang, B.3
Steel, P.J.4
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45
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34848924716
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note
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20 +9.4 (c 0.2, EtOH). See Refs. 7 and 8.
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