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1
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0037459890
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Recent reviews: [1a] P. M. Weintraub, J. S. Sabol, J. M. Kane, D. R. Borcherding, Tetrahedron 2003, 59, 2953-2989.
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Weintraub, P.M.1
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3
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0033431540
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H.-P. Husson, J. Royer, Chem. Soc., Rev. 1999, 28, 383-394.
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Husson, H.-P.1
Royer, J.2
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4
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0002942604
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Preparation of 1: M. Bonin, D. S. Grierson, J. Royer, H.-P. Husson, Org. Synth. 1991, 70, 54-59.
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Bonin, M.1
Grierson, D.S.2
Royer, J.3
Husson, H.-P.4
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5
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0034689892
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For representative examples, see: [3a] F. A. Davis, B. Chao, T. Fang, J. M. Szewczyk, Org. Lett. 2000, 2, 1041-1043.
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Davis, F.A.1
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0037131150
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[3b] C. Agami, L. Dechoux, C. Ménard, S. Hebbe, J. Org. Chem. 2002, 67, 7573-7576.
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Agami, C.1
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7
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0036827950
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[3c] M. K. S. Vink, C. A. Schortinghuis, J. Luten, J. H. van Maarseveen, H. E. Schoemaker, H. Hiemstra, F. P. J. T. Rutjes, J. Org. Chem. 2002, 67, 7869-7871.
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Vink, M.K.S.1
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0037424287
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[3d] M. Amat, N. Llor, J. Hidalgo, C. Escolano, J. Bosch, J. Org. Chem. 2003, 68, 1919-1928.
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Amat, M.1
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9
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0001329009
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Representative example, see: S. Arseniyadis, P. Q. Huang, D. Piveteau, H.-P. Husson, Tetrahedron 1988, 44, 2457-2470.
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Arseniyadis, S.1
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Piveteau, D.3
Husson, H.-P.4
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11
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0021079132
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[6a] L. Guerrier, J. Royer, D. S. Grierson, H.-P. Husson, J. Am. Chem. Soc. 1983, 705, 7754-7755.
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Guerrier, L.1
Royer, J.2
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Husson, H.-P.4
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16
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0342483671
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K. Ogura, Y. Shimamura, M. Fujita, J. Org. Chem. 1991, 56, 2920-2922.
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Ogura, K.1
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0032560715
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J. E. Baldwin, D. R. Spring, R. C. Whitehead, Tetrahedron Lett. 1998, 39, 5417-5420.
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Baldwin, J.E.1
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0010338892
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S.-I. Yamada, K. Tomioka, K. Koga, Tetrahedron Lett. 1976, 1, 61-64.
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Yamada, S.-I.1
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Koga, K.3
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20
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0029848930
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O. Froelich, P. Desos, M. Bonin, J.-C. Quirion, H.-P. Husson, J. Zhu, J. Org. Chem. 1996, 61, 6700-6705.
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Froelich, O.1
Desos, P.2
Bonin, M.3
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Husson, H.-P.5
Zhu, J.6
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21
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0030037070
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C. Yue, I. Gauthier, J. Royer, H.-P. Husson, J. Org. Chem. 1996, 61, 4949-4954.
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J. Org. Chem.
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Yue, C.1
Gauthier, I.2
Royer, J.3
Husson, H.-P.4
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22
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0042865038
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D. François, E. Poupon, M.-C. Lallemand, N. Kunesch, H.-P. Husson, J. Org. Chem. 2000, 65, 3209-3212.
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J. Org. Chem.
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François, D.1
Poupon, E.2
Lallemand, M.-C.3
Kunesch, N.4
Husson, H.-P.5
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23
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0001394411
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H. Poerwono, K. Higashiyama, T. Yamauchi, H. Takahashi, Heterocycles 1997, 46, 385-400.
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Poerwono, H.1
Higashiyama, K.2
Yamauchi, T.3
Takahashi, H.4
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24
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0034693192
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E. Poupon, B.-X. Luong, A. Chiaroni, N. Kunesch, H.-P. Husson, J. Org. Chem. 2000, 65, 7208-7210.
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J. Org. Chem.
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Poupon, E.1
Luong, B.-X.2
Chiaroni, A.3
Kunesch, N.4
Husson, H.-P.5
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27
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1542353892
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-
L. Belvisi, A. Bernardi, A. Checchia, L. Manzoni, D. Potenza, C. Scolastico, M. Castorina, A. Cupelli, G. Giannini, P. Carminati, C. Pisano, Org. Lett. 2001, 3, 1001-1004.
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Belvisi, L.1
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Castorina, M.7
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Giannini, G.9
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Pisano, C.11
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28
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10844293712
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Drugs Fut. 1999, 24, 577.
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Drugs Fut.
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29
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0033571278
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B. Westermann, A. Walter, N. Diedrichs, Angew. Chem. Int. Ed. 1999, 38, 3384-3386.
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Westermann, B.1
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Diedrichs, N.3
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30
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0033590937
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[23a] K. M. Muller, A. Schoenfelder, B. Didier, A. Mann, C.-G. Wermuth, Chem. Commun. 1999, 683-684.
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Muller, K.M.1
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Mann, A.4
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31
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4544304723
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[23b] J. Marin, A. Violette, J.-P. Briand, G. Guichard, Eur. J. Org. Chem. 2004, 3027-3039.
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Marin, J.1
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Briand, J.-P.3
Guichard, G.4
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32
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0033404658
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[24a] K. Akasaka, H. Akamatsu, Y. Kimoto, Y. Komatsu, T. Shimizu, N. Shimomura, K. Tagami, S. Negi, Chem. Pharm. Bull. 1999, 47, 1525-1531.
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Akasaka, K.1
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Kimoto, Y.3
Komatsu, Y.4
Shimizu, T.5
Shimomura, N.6
Tagami, K.7
Negi, S.8
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33
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0033430928
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K. Akasaka, Y. Komatsu, K. Tagami, T. Shimizu, N. Shimomura, H. Naka, K. Hayashi, S. Negi, Chem. Pharm. Bull. 1999, 47, 1532-1537.
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Akasaka, K.1
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Tagami, K.3
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Shimomura, N.5
Naka, H.6
Hayashi, K.7
Negi, S.8
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35
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0037060982
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[25b] S. Hanessian, W. A. L. van Otterlo, I. Nilsson. U. Bauer, Tetrahedron Lett. 2002, 43, 1995-1998.
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Hanessian, S.1
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84862700586
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P. Liénard, T. Varea, J.-C. Quirion, H.-P. Husson, Synlett 1994, 143-144.
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Liénard, P.1
Varea, T.2
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Husson, H.-P.4
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38
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0001132028
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A. Cave. C. Kan-Fan, P. Potier, J. Le Men, M. M. Janot. Tetrahedron 1967, 23, 4691-4696.
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Cave, A.1
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Potier, P.3
Le Men, J.4
Janot, M.M.5
-
39
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0030602244
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[29a] It should be noted that this compound has previously been prepared in our group by electrochemistry (85% yield on a 110-mg scale), see: F. Billon-Souquet, T. Martens, J. Royer, Tetrahedron 1996, 52, 15127-15136.
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Tetrahedron
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Billon-Souquet, F.1
Martens, T.2
Royer, J.3
-
40
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0037867664
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-
[29b] For a recent two-step synthesis (470-mg scale), see: M. Amat, C. Escolano. N. Llor, M. Husuet. M. Férez. J. Bosch, Tetrahedron: Asymmetry 2003, 14, 1679-1683.
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Tetrahedron: Asymmetry
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Amat, M.1
Escolano, C.2
Llor, N.3
Husuet, M.4
Férez, M.5
Bosch, J.6
-
41
-
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0028314897
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-
Previous synthesis, see: L. Micouin, T. Varea, C. Riche. A. Chiaroni, J.-C. Quirion. H.-P. Husson, Tetrahedron Lett. 1994, 35, 2529-2532.
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(1994)
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Micouin, L.1
Varea, T.2
Riche, C.3
Chiaroni, A.4
Quirion, J.-C.5
Husson, H.-P.6
-
42
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0001046290
-
-
[31a] Obtained as a 75:25 mixture of epimers in favor of the β-oxazolidine. First description of this laetam: J. Royer. H.-P. Husson. Heterocycles 1993, 36, 1493-1496.
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(1993)
Heterocycles
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-
Royer, J.1
Husson, H.-P.2
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43
-
-
0038498498
-
-
and references cited therein
-
[31b] For recent synthetic applications, see: N. Casamitjana, M. Amat, N. Llor, M. Carreras, X. Pujol, M. M. Fernández, V. López, E. Molins, C. Miravitlles, J. Bosch. Tetrahedron: Asymmetry 2003. 14, 2033-2039 and references cited therein.
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Tetrahedron: Asymmetry
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-
Casamitjana, N.1
Amat, M.2
Llor, N.3
Carreras, M.4
Pujol, X.5
Fernández, M.M.6
López, V.7
Molins, E.8
Miravitlles, C.9
Bosch, J.10
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44
-
-
0037423124
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[31c] M. Amat, N. Llor. C. Escolano, M. Huguet, M. Pérez, E. Molins, J. Bosch. Tetrahedron: Asymmetry 2003, 14, 293-295.
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(2003)
Tetrahedron: Asymmetry
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, pp. 293-295
-
-
Amat, M.1
Llor, N.2
Escolano, C.3
Huguet, M.4
Pérez, M.5
Molins, E.6
Bosch, J.7
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45
-
-
0001203714
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-
[32a] P. Q. Huang, S. Arseniyadis, H.-P Husson, Tetrahedron Lett. 1987, 28, 547-550.
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(1987)
Tetrahedron Lett.
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Huang, P.Q.1
Arseniyadis, S.2
Husson, H.-P.3
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47
-
-
0028124306
-
-
1H NMR evaluation), see: J.-F. Berrien, J. Royer. H.-P. Husson, J. Org. Chem. 1994, 59, 3769-3774.
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(1994)
J. Org. Chem.
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Berrien, J.-F.1
Royer, J.2
Husson, H.-P.3
-
48
-
-
10844263719
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-
note
-
7:3 ratio of epimers.
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-
-
-
50
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0034605811
-
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6-Alkylpiperidin-2-one (de 75%): [35b] F. Bois, D. Gardette, J.-C. Gramain, Tetrahedron Un. 2000, 41, 8769-8772.
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(2000)
Tetrahedron Un.
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Bois, F.1
Gardette, D.2
Gramain, J.-C.3
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51
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0035126636
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[35c] For other examples of synthesis of N-protected oxopipecolates without reference to optical purity, see: I. G. C. Coutts, R. E. Saint, S. L. Saint, D. M. Chambers-Asman, Synthesis 2001, 247-250.
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(2001)
Synthesis
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-
Coutts, I.G.C.1
Saint, R.E.2
Saint, S.L.3
Chambers-Asman, D.M.4
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52
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0000432183
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[35d] N-Protected 6-alkylpiperidin-2-ones: J. R. Casimir, C. Didierjean, A. Aubry. M. Rodriguez, J.-P. Briand, G. Guichard, Org. Lett. 2000, 2, 895-897.
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Org. Lett.
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Casimir, J.R.1
Didierjean, C.2
Aubry, A.3
Rodriguez, M.4
Briand, J.-P.5
Guichard, G.6
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53
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0346969559
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[36a] Recent examples: A. A. Bahajaj, M. H. Moore, J. M. Vernon, Tetrahedron 2004, 60, 1235-1246.
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(2004)
Tetrahedron
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Bahajaj, A.A.1
Moore, M.H.2
Vernon, J.M.3
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54
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0348230513
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[36b] A. A. Bahajaj, J. M. Vernon, G. D. Wilson, Tetrahedron 2004, 60, 1247-1253.
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Tetrahedron
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Bahajaj, A.A.1
Vernon, J.M.2
Wilson, G.D.3
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55
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2342483687
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For recent and efficient alkylations of enantiopure bicyclic piperidones derived from 6-oxopipecolic acid, see: A. G. Brewster, S. Broady, C. E. Davies, T. D. Heightman, S. A. Hermitage, M. Hughes, M. G. Moloney. G. Woods. Org. Biomol. Chem. 2004. 2, 1031-1043.
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Brewster, A.G.1
Broady, S.2
Davies, C.E.3
Heightman, T.D.4
Hermitage, S.A.5
Hughes, M.6
Moloney, M.G.7
Woods, G.8
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