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A. de Meijere, K. Ernst, B. Zuck, M. Brandl, S. I. Kozhushkov, M. Tamm, D. S. Yufit, J. K. Howard, T. Labahn, Eur. J. Org. Chem. 1999, in press, and Part 5: ref. [12a].
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De Meijere, A.1
Ernst, K.2
Zuck, B.3
Brandl, M.4
Kozhushkov, S.I.5
Tamm, M.6
Yufit, D.S.7
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a) D. Seebach, Angew. Chem. 1990, 102, 1363-1409; Angew. Chem. Int. Ed. Engl. 1990, 29, 1320-1365;
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Seebach, D.1
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a) D. Seebach, Angew. Chem. 1990, 102, 1363-1409; Angew. Chem. Int. Ed. Engl. 1990, 29, 1320-1365;
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5
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0028318863
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For analogous solid-phase reactions, see: a) E. M. Gordon, R. W. Barrett, W. J. Dower, S. P. A. Fodor, M. A. Gallop, J. Med. Chem. 1994, 37, 1385-1401;
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c) J. S. Früchtel, G. Jung, Angew. Chem. 1996, 108, 19-46; Angew. Chem. Int. Ed. Engl. 1996, 35, 17-42;
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Früchtel, J.S.1
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0003180602
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c) J. S. Früchtel, G. Jung, Angew. Chem. 1996, 108, 19-46; Angew. Chem. Int. Ed. Engl. 1996, 35, 17-42;
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9
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0000312967
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d) F. Balkenhohl, C. von dem Bussche-Hünnefeld, A. Lansky, C. Zechel, Angew. Chem. 1996, 108, 2437-2487; Angew. Chem. Int. Ed. Engl. 1996, 35, 2288-2337;
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Balkenhohl, F.1
Von Dem Bussche-Hünnefeld, C.2
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Zechel, C.4
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d) F. Balkenhohl, C. von dem Bussche-Hünnefeld, A. Lansky, C. Zechel, Angew. Chem. 1996, 108, 2437-2487; Angew. Chem. Int. Ed. Engl. 1996, 35, 2288-2337;
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e) P. H. H. Hermkens, H. C. J. Ottenheijm, D. C. Rees, Tetrahedron 1997, 53, 5643-5678;
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Hermkens, P.H.H.1
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13
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0004041610
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Eds.: S. R. Wilson, A. W. Czarnik, Wiley-Interscience, New York, and references therein
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g) Combinatorial Chemistry (Eds.: S. R. Wilson, A. W. Czarnik), Wiley-Interscience, New York, 1997, and references therein.
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Combinatorial Chemistry
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14
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0001237986
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Review: L. F. Tietze, U. Beifuss, Angew. Chem. 1993, 105, 137-170; Angew. Chem. Int. Ed. Engl. 1993, 32, 131-164.
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Tietze, L.F.1
Beifuss, U.2
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Review: L. F. Tietze, U. Beifuss, Angew. Chem. 1993, 105, 137-170; Angew. Chem. Int. Ed. Engl. 1993, 32, 131-164.
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Angew. Chem. Int. Ed. Engl.
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18
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0032537030
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c) D. G. Powers, D. S. Casebier, D. Fokas, W. J. Ryan, J. R. Troth, D. L. Coffen, Tetrahedron 1998, 54, 4085-4096.
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Tetrahedron
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Powers, D.G.1
Casebier, D.S.2
Fokas, D.3
Ryan, W.J.4
Troth, J.R.5
Coffen, D.L.6
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19
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0000609674
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D. P. Curran, Angew. Chem. 1998, 110, 1230-1255; Angew. Chem. Int. Ed. 1998, 37, 1174-1196.
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Curran, D.P.1
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20
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0032543080
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D. P. Curran, Angew. Chem. 1998, 110, 1230-1255; Angew. Chem. Int. Ed. 1998, 37, 1174-1196.
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Angew. Chem. Int. Ed.
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21
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0029940759
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a) Ugi reaction: A. M. M. Mjalli, S. Sarshar, T. J. Baiga, Tetrahedron Lett. 1996, 37, 2943-2946;
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Tetrahedron Lett.
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Mjalli, A.M.M.1
Sarshar, S.2
Baiga, T.J.3
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22
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0030038838
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b) Biginelli reaction: M. F. Gordeev, D. V. Patel, E. M. Gordon, J. Org. Chem. 1996, 61, 924-928;
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Gordeev, M.F.1
Patel, D.V.2
Gordon, E.M.3
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23
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0032567888
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c) Mannich reaction: J. J. McNally, M. A. Youngman, S. L. Dax, Tetrahedron Lett. 1998, 39, 967-970;
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McNally, J.J.1
Youngman, M.A.2
Dax, S.L.3
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24
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0032567960
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d) Robinson multicomponent reaction: D. Jönsson, H. Molin, A. Undén, Tetrahedron Lett. 1998, 39, 1059-1062;
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Tetrahedron Lett.
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Jönsson, D.1
Molin, H.2
Undén, A.3
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27
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0000847293
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S. Bräse, A. de Meijere, Angew. Chem. 1995, 107, 2741-2743; Angew. Chem. Int. Ed. Engl. 1995, 34, 2545-2547.
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Angew. Chem.
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Bräse, S.1
De Meijere, A.2
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28
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33748241772
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S. Bräse, A. de Meijere, Angew. Chem. 1995, 107, 2741-2743; Angew. Chem. Int. Ed. Engl. 1995, 34, 2545-2547.
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29
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0343918798
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note
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4 (406.5): C 76.82, H 7.44; found: C 76.65, H 7.43.
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-
-
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32
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0343918795
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note
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2 using the least-squares method. All non-hydrogen atoms were refined anisotropically. All hydrogen atoms were placed in geometrically ideal positions and included in the refinement. All disorders were resolved and refined anisotropically with the help of space and ADP restraints. Crystallographic data (excluding structure factors) of the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-133154 (4f) and CCDC-133155 (5). Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: (+44)1223-336-033; e-mail: deposit@ccdc.cam.ac.uk).
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-
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33
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0002000906
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The bicyclopropylidene component can also be varied as numerous substituted bicyclopropylidenes are now readily available in greater quantities. Review: A. de Meijere, S. I. Kozhushkov, A. F. Khlebnikov, Topics Curr. Chem. 1999, 207, 89-147.
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De Meijere, A.1
Kozhushkov, S.I.2
Khlebnikov, A.F.3
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34
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0039993764
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a) S. Bräse, M. Schroen, Angew. Chem. 1999, 111, 1139-1142; Angew. Chem. Int. Ed. 1999, 38, 1071-1073;
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Bräse, S.1
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35
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0033583489
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a) S. Bräse, M. Schroen, Angew. Chem. 1999, 111, 1139-1142; Angew. Chem. Int. Ed. 1999, 38, 1071-1073;
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36
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b) S. Bräse, D. Enders, J. Köbberling, F. Avemaria, Angew. Chem. 1998, 110, 3614-3616; Angew. Chem. Int. Ed. 1998, 37, 3413-3415;
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Bräse, S.1
Enders, D.2
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37
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b) S. Bräse, D. Enders, J. Köbberling, F. Avemaria, Angew. Chem. 1998, 110, 3614-3616; Angew. Chem. Int. Ed. 1998, 37, 3413-3415;
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38
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4244196819
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Eds.: E. Pombo-Villar, R. Neier, S.-K. Lin, CD-ROM Edition (ISBN 3-906980-04-9), MDPI, Basel
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c) Review: S. Bräse, S. Dahmen, M. Lormann in Proceedings of ECSOC-3, The Third International Electronic Conference on Synthetic Organic Chemistry (Eds.: E. Pombo-Villar, R. Neier, S.-K. Lin), CD-ROM Edition (ISBN 3-906980-04-9), MDPI, Basel, 1999;
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Proceedings of ECSOC-3, The Third International Electronic Conference on Synthetic Organic Chemistry
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Bräse, S.1
Dahmen, S.2
Lormann, M.3
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40
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0002314205
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Eds.: F. Diederich, P. J. Stang, Wiley-VCH, Weinheim, and references therein
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S. Bräse, A. de Meijere in Metal-catalyzed Cross-coupling Reactions (Eds.: F. Diederich, P. J. Stang), Wiley-VCH, Weinheim, 1998, pp. 99-167, and references therein.
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Metal-catalyzed Cross-coupling Reactions
, pp. 99-167
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Bräse, S.1
De Meijere, A.2
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41
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85039384284
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A control experiment under standard pressure only produced methyl p-(3-cyclopentyl)cinnamate in 68% yield (after the subsequent Heck reaction). The application of high pressure promotes the Heck as well as the Diels-Alder reaction: K. Voigt, U. Schick, F. E. Meyer, A. de Meijere, Synlett 1994, 189-190.
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(1994)
Synlett
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Voigt, K.1
Schick, U.2
Meyer, F.E.3
De Meijere, A.4
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42
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0343918792
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note
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13C NMR, IR, MS, elemental analysis, or HR-MS), known compounds were identified by comparison of the spectroscopic data.
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