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Maas, G.1
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0001133088
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Hopf, H.1
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b) H. Hopf, G. Maas, Angew. Chem. 1992, 104, 953-977; Angew. Chem. Int. Ed. Engl. 1992, 31, 931-954.
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a) A. M. Boldi, F. Diederich. Angew. Chem. 1994, 106, 482-485; Angew. Chem. Int. Ed. Engl. 1994, 33, 468-471;
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a) A. M. Boldi, F. Diederich. Angew. Chem. 1994, 106, 482-485; Angew. Chem. Int. Ed. Engl. 1994, 33, 468-471;
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b) J. Anthony, A. M. Boldi, C. Boudon, J.-P. Gisselbrecht, M. Gross, P. Seiler, C. B. Knobler, F. Diederieh, Helv. Chim. Acta 1995, 78, 797-817;
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7
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0031102335
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c) M. Schreiber, R. R. Tykwinski, F. Diederich, R. Spreiter, U Gubler, C. Bosshard, I. Poberaj, P. Günter, C. Boudon, J.-P. Gisselbrecht, M. Gross, U. Jonas, H. Ringsdorf, Adv. Mater. 1997, 9, 339-343.
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Gross, M.11
Jonas, U.12
Ringsdorf, H.13
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8
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0000807918
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Other examples of cross-conjugated macrocycles: a) A. Sekiguchi, T. Matsuo, H. Sakurai, Angew. Chem. 1998, 110, 1751-1754; Angew. Chem. Int. Ed. 1998, 37, 1662-1664;
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Sekiguchi, A.1
Matsuo, T.2
Sakurai, H.3
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9
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85080847923
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Other examples of cross-conjugated macrocycles: a) A. Sekiguchi, T. Matsuo, H. Sakurai, Angew. Chem. 1998, 110, 1751-1754; Angew. Chem. Int. Ed. 1998, 37, 1662-1664;
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10
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0001993629
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b) S. Kammermeier, R. R. Tykwinski, P. Siemsen, P. Seiler, F. Diederich, Chem. Commun. 1998, 1285-1286;
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Kammermeier, S.1
Tykwinski, R.R.2
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Seiler, P.4
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d) A. Stanger, N. Ashkenazi, R. Boese, D. Bläser, P. Stellberg, Chem. Eur. J. 1997, 3, 208-211;
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Bläser, D.4
Stellberg, P.5
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13
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e) T. Enomoto, T. Kawase, H. Kurata, M. Oda, Tetrahedron Lett. 1997, 38, 2693-2696;
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Tetrahedron Lett.
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Enomoto, T.1
Kawase, T.2
Kurata, H.3
Oda, M.4
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14
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0028953447
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f) R. Gleiter, H. Röckel, B. Nuber, Tetrahedron Lett. 1995, 36, 1835-1838;
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Gleiter, R.1
Röckel, H.2
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15
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g) R. Faust, F. Diederich, V. Gramlich, P. Setler, Chem. Eur. J. 1995, 1, 117;
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Faust, R.1
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Gramlich, V.3
Setler, P.4
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16
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0344070841
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h) R. Gleiter, H. Röckel, H. Irngartinger, T. Oeser, Angew. Chem. 1994, 106, 1340-1342; Angew. Chem. Int. Ed. Engl. 1994, 33, 1270-1272;
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Gleiter, R.1
Röckel, H.2
Irngartinger, H.3
Oeser, T.4
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17
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33748240680
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h) R. Gleiter, H. Röckel, H. Irngartinger, T. Oeser, Angew. Chem. 1994, 106, 1340-1342; Angew. Chem. Int. Ed. Engl. 1994, 33, 1270-1272;
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25
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0344070839
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note
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13C NMR, IR, UV, MS, and either elemental analysis or HR-MS.
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27
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1542603521
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D. A. Shultz, K. P. Gwaltney, H. Lee, J. Org. Chem. 1998, 63, 4034-4038.
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Shultz, D.A.1
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Lee, H.3
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28
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3843060889
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R. Hässig, D. Seebach, H. Siegel, Chem. Ber. 1984, 117, 1877-1884.
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Chem. Ber.
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Hässig, R.1
Seebach, D.2
Siegel, H.3
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29
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0344502035
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note
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[13) The absorption band for the transoid form at 305 nm, visible as a shoulder in the spectrum of 10, is more clearly discernible in 9 and other shorter iso-PDAs. [5]
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30
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0345364347
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note
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2 with Macromodel 5.5.
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31
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0000154678
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(Eds.: P. J. Stang, F. Diederich), VCH. Weinheim
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For a similar discussion of homoconjugation in percyclines, see L. T. Scott, M. J. Cooney in Modern Acetylene Chemistry (Eds.: P. J. Stang, F. Diederich), VCH. Weinheim, 1995, pp. 321-351.
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(1995)
Modern Acetylene Chemistry
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Scott, L.T.1
Cooney, M.J.2
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32
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0001609215
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M. Iyoda, S. Tanaka, H. Otani, M. Nose, M. Oda, J. Am. Chem. Soc. 1988, 110, 8494-8500.
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J. Am. Chem. Soc.
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Iyoda, M.1
Tanaka, S.2
Otani, H.3
Nose, M.4
Oda, M.5
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33
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0345364346
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note
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[10] to give 13 as a colorless solid.
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-
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34
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0345364345
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note
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[10] to give 15 as a white solid.
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