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1
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0003982088
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For a monograph on piperidone chemistry see: Elsevier, Amsterdam
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a) For a monograph on piperidone chemistry see: M. Rubiralta, E. Giralt, A. Diez, Piperidine. Structure, Preparation, Reactivity and Synthetic Applications of Piperidine and its Derivatives, Elsevier, Amsterdam, 1991.
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Piperidine. Structure, Preparation, Reactivity and Synthetic Applications of Piperidine and Its Derivatives
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Rubiralta, M.1
Giralt, E.2
Diez, A.3
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2
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0040479831
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b) M. Rubiralta, A. Diez, C. Vila, Y. Troin, M. Feliz, J. Org. Chem. 1991, 56, 6292-6298.
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J. Org. Chem.
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Rubiralta, M.1
Diez, A.2
Vila, C.3
Troin, Y.4
Feliz, M.5
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4
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0003022837
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d) A. Diez, S. Mavel, J. C. Teulade, O. Chavignon, M. E. Sinibaldi, Y. Troin, M. Rubiralta, Heterocycles 1993, 36, 2451-2463.
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Heterocycles
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Diez, A.1
Mavel, S.2
Teulade, J.C.3
Chavignon, O.4
Sinibaldi, M.E.5
Troin, Y.6
Rubiralta, M.7
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5
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0027941124
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e) J. Gracia, N. Casamitjana, J. Bonjoch, J. Bosch, J. Org. Chem. 1994, 59, 3939-3951.
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J. Org. Chem.
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Gracia, J.1
Casamitjana, N.2
Bonjoch, J.3
Bosch, J.4
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6
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0022972078
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a) F. Janssens, J. Torremans, P. A. J. Janssen, J. Med. Chem. 1986, 29, 2290-2297.
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J. Med. Chem.
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Janssens, F.1
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7
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0024507397
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b) J. R. Bagley, R. L. Wynn, F. G. Rudo, B. M. Doorley, H. K. Spencer, T. Spaulding, ibid. 1989, 32, 663-671.
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Bagley, J.R.1
Wynn, R.L.2
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8
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c) L. V. Kudzma, S. A. Severnak, M. J. Benvenga, E. F. Ezell, M. H. Ossipov, V. V. Knight, F. G. Rudo, H. K. Spencer, T. C. Spaulding, ibid. 1989, 32, 2534-2542.
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Ibid.
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Kudzma, L.V.1
Severnak, S.A.2
Benvenga, M.J.3
Ezell, E.F.4
Ossipov, M.H.5
Knight, V.V.6
Rudo, F.G.7
Spencer, H.K.8
Spaulding, T.C.9
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9
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25144445524
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G. V. Grishina, V. M. Potapov, S. A. Abdulganeeva, T. A. Gudasheva, I. F. Leshcheva, N. M. Sergeev, T. A. Kudryavtseva, E. Y. Korchagina, Khim Geterotzikl. Soedin. 1983, 1693-1694.
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Khim Geterotzikl. Soedin.
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Grishina, G.V.1
Potapov, V.M.2
Abdulganeeva, S.A.3
Gudasheva, T.A.4
Leshcheva, I.F.5
Sergeev, N.M.6
Kudryavtseva, T.A.7
Korchagina, E.Y.8
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10
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25144445524
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G. V. Grishina, S. A. Abdulganeeva, V. M. Potapov, I. A. Ivanova, A. A. Espenbetov, Y. T. Strychkov, I. A. Grishina, A. I. Lutsenko, Khim Geterotzikl. Soedin. 1985, 1656-1662.
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Khim Geterotzikl. Soedin.
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Grishina, G.V.1
Abdulganeeva, S.A.2
Potapov, V.M.3
Ivanova, I.A.4
Espenbetov, A.A.5
Strychkov, Y.T.6
Grishina, I.A.7
Lutsenko, A.I.8
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13
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0039886961
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M. Rubiralta, A. Diez, C. Vila, J. Castells, I. López, Heterocycles 1992, 34, 643-650.
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(1992)
Heterocycles
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Rubiralta, M.1
Diez, A.2
Vila, C.3
Castells, J.4
López, I.5
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14
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0003719612
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For some leading references see: a Academic Press, Orlando
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For some leading references see: a) D. L. Boger, S. M. Weinreb, Hetero-Diels-Alder Methodology in Organic Synthesis, Academic Press, Orlando, 1987, pp. 35-71.
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Hetero-Diels-Alder Methodology in Organic Synthesis
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Boger, D.L.1
Weinreb, S.M.2
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18
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33749089348
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b) H. Waldmann, M. Braun, M. Dräger, Angew. Chem. Int. Ed. Engl. 1990, 29, 1468-1471.
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Angew. Chem. Int. Ed. Engl.
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Waldmann, H.1
Braun, M.2
Dräger, M.3
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20
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0027522894
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d) A. K. McFarlane, G. Thomas, A. Whiting, Tetrahedron Lett. 1993, 34, 2379-2382.
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Tetrahedron Lett.
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McFarlane, A.K.1
Thomas, G.2
Whiting, A.3
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21
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0002836654
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e) K. Ishimaru, K. Watanabe, Y. Yamamoto, K. Akiba, Synlett, 1994, 495-498.
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Synlett
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Ishimaru, K.1
Watanabe, K.2
Yamamoto, Y.3
Akiba, K.4
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24
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0000998435
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J. Barluenga, F. Aznar, C. Valdés, M. P. Cabal, J. Org. Chem. 1993, 58, 3391-3396.
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J. Org. Chem.
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Barluenga, J.1
Aznar, F.2
Valdés, C.3
Cabal, M.P.4
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25
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0000651283
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a) J. Barluenga, F. Aznar, C. Valdés, A. Martín, S. García-Granda, E. Martín, J. Am. Chem. Soc. 1993, 115, 4403-4404.
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Barluenga, J.1
Aznar, F.2
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Martín, E.6
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26
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37049084201
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b) J. Barluenga, F. Aznar, A. Martín, S. Barluenga, S. García-Granda, A. A. Paneque-Quevedo, J. Chem. Soc. Chem. Commun. 1994, 843-844.
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J. Chem. Soc. Chem. Commun.
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Barluenga, J.1
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Paneque-Quevedo, A.A.6
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28
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0028203787
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d) D. Enders, O. Meyer, G. Raabe, J. Runsink, ibid. 1994, 66-72.
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Synthesis
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Enders, D.1
Meyer, O.2
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Runsink, J.4
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29
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0040368147
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J. Barluenga, F. Aznar, C. Valdés, M. P. Cabal, J. Org. Chem. 1991, 56, 6166-6171.
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J. Org. Chem.
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Barluenga, J.1
Aznar, F.2
Valdés, C.3
Cabal, M.P.4
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30
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84891287564
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note
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4J(H 3,H 5) = 1.3 Hz] is observed due to the planar W geometry.
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33
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84891288667
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Serena Software: P. O. Box 3076, Bloomington, IN 47402-3076
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MMX force field. PCMODEL-PI (v 4.0), Serena Software: P. O. Box 3076, Bloomington, IN 47402-3076.
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MMX Force Field. PCMODEL-PI (v 4.0)
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34
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84891280959
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note
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The strain energy differences, rotamer distributions, and especially dihedral angles O4-C4-C7-O7 found for the rotamers of compound 13 are of great interest for CD analysis.
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35
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84891309956
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note
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-1 and HPLC grade n-hexane/EtOAc (85:15) solvent system.
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37
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2142858450
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For some recent examples: a
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For some recent examples: a) I. Othani, T. Kusumi, Y. Kashman, H. Kasikawa, J. Am. Chem. Soc. 1991, 113, 4092-4096.
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J. Am. Chem. Soc.
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Othani, I.1
Kusumi, T.2
Kashman, Y.3
Kasikawa, H.4
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38
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0025968542
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b) E. Finamore, L. Minale, R. Riccio, G. Rinaldo, F. Zollo, J. Org. Chem. 1991, 56, 1146-1153.
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J. Org. Chem.
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Finamore, E.1
Minale, L.2
Riccio, R.3
Rinaldo, G.4
Zollo, F.5
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39
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0026758840
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c) J. Rodríguez, R. Riguera, C. Debitus, ibid. 1992, 57, 4624-4632.
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J. Org. Chem.
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Rodríguez, J.1
Riguera, R.2
Debitus, C.3
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42
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33845469454
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For MOM, see
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For MOM, see L. Banfi, A. Bernardi, L. Colombo, C. Gennari, C. Scolastico J. Org. Chem. 1984, 49, 3784-3790.
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J. Org. Chem.
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Banfi, L.1
Bernardi, A.2
Colombo, L.3
Gennari, C.4
Scolastico, C.5
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44
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0023915664
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E. W. Colvin, D. McGarry, M. J. Nugent, Tetrahedron 1988, 44, 4157-4172.
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Tetrahedron
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Colvin, E.W.1
McGarry, D.2
Nugent, M.J.3
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