-
1
-
-
0000787447
-
-
Bartlett, P. D., Ryan, M. J., and Cohen, S. G. J. Am. Chem. Soc. 1942, 64, 2649
-
(1942)
J. Am. Chem. Soc.
, vol.64
, pp. 2649
-
-
Bartlett, P.D.1
Ryan, M.J.2
Cohen, S.G.3
-
2
-
-
36948999794
-
-
Hart, H., Bashir-Hashemi, A., Luo, J., and Meador, M. A. Tetrahedron 1986, 42, 1641
-
(1986)
Tetrahedron
, vol.42
, pp. 1641
-
-
Hart, H.1
Bashir-Hashemi, A.2
Luo, J.3
Meador, M.A.4
-
6
-
-
33744467395
-
-
Chen, Z., Amara, J. P., Thomas, S. W., III, and Swager, T. M. Macromolecules 2006, 39, 3202
-
(2006)
Macromolecules
, vol.39
, pp. 3202
-
-
Chen, Z.1
Amara, J.P.2
Thomas III, S.W.3
Swager, T.M.4
-
7
-
-
0033954012
-
-
Yang, J.-S., Lee, C.-C., Yau, S.-L., Chang, C.-C., Lee, C.-C., and Leu, J.-M. J. Org. Chem. 2000, 65, 871
-
(2000)
J. Org. Chem.
, vol.65
, pp. 871
-
-
Yang, J.-S.1
Lee, C.-C.2
Yau, S.-L.3
Chang, C.-C.4
Lee, C.-C.5
Leu, J.-M.6
-
9
-
-
0035148647
-
-
Gust, D., Moore, T. A., and Moore, A. L. Acc. Chem. Res. 2001, 34, 40
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 40
-
-
Gust, D.1
Moore, T.A.2
Moore, A.L.3
-
10
-
-
0035905115
-
-
Wiehe, A., Senge, M. O., Schafer, A., Speck, M., Tannert, S., Kurreck, H., and Roder, B. Tetrahedron 2001, 57, 10089
-
(2001)
Tetrahedron
, vol.57
, pp. 10089
-
-
Wiehe, A.1
Senge, M.O.2
Schafer, A.3
Speck, M.4
Tannert, S.5
Kurreck, H.6
Roder, B.7
-
11
-
-
0037657920
-
-
Springer, J., Kodis, G., De la Garza, L., Moore, A. L., Moore, T. A., and Gust, D. J. Phys. Chem. A 2003, 107, 3567
-
(2003)
J. Phys. Chem. A
, vol.107
, pp. 3567
-
-
Springer, J.1
Kodis, G.2
De La Garza, L.3
Moore, A.L.4
Moore, T.A.5
Gust, D.6
-
15
-
-
33745815692
-
-
Hua, D. H., Lou, K., Battina, S. K., Zhao, H., Perchellet, E. M., Wang, Y., and Perchellet, J.-P. Anti-Cancer Agents Med. Chem. 2006, 6, 303
-
(2006)
Anti-Cancer Agents Med. Chem.
, vol.6
, pp. 303
-
-
Hua, D.H.1
Lou, K.2
Battina, S.K.3
Zhao, H.4
Perchellet, E.M.5
Wang, Y.6
Perchellet, J.-P.7
-
17
-
-
37049111529
-
-
Alder, R. W. and Sessions, R. B. J. Chem. Soc., Perkin Trans. 2. 1985, 11, 1849
-
(1985)
J. Chem. Soc., Perkin Trans. 2.
, vol.11
, pp. 1849
-
-
Alder, R.W.1
Sessions, R.B.2
-
18
-
-
78650160718
-
-
For a recent review, see
-
For a recent review, see
-
-
-
-
19
-
-
77954927278
-
-
Eisenberg, D., Shenhar, R., and Rabinovitz, M. Chem. Soc. Rev. 2010, 39, 2879
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 2879
-
-
Eisenberg, D.1
Shenhar, R.2
Rabinovitz, M.3
-
20
-
-
11944267916
-
-
Ashton, P. R., Brown, G. R., Isaacs, N. C., Giuffrida, D., Kohnke, F. H., Mathias, J. P., Slawin, A. M. Z., Smith, D. R., Stoddart, J. F., and Williams, D. J. J. Am. Chem. Soc. 1992, 114, 6330
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 6330
-
-
Ashton, P.R.1
Brown, G.R.2
Isaacs, N.C.3
Giuffrida, D.4
Kohnke, F.H.5
Mathias, J.P.6
Slawin, A.M.Z.7
Smith, D.R.8
Stoddart, J.F.9
Williams, D.J.10
-
21
-
-
19944362262
-
-
Benkhoff, J., Boese, R., and Klarner, F.-G. Liebigs Ann. Recl. 1997, 501
-
(1997)
Liebigs Ann. Recl.
, pp. 501
-
-
Benkhoff, J.1
Boese, R.2
Klarner, F.-G.3
-
24
-
-
78650100366
-
-
The single-crystal X-ray structure of compound 2 has not been reported previously. The authors have deposited atomic coordinates for the structures, compound 2 and 1a with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 175022. The coordinates can be obtained on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K
-
The single-crystal X-ray structure of compound 2 has not been reported previously. The authors have deposited atomic coordinates for the structures, compound 2 and 1a with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 175022. The coordinates can be obtained on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K.
-
-
-
-
27
-
-
85082714011
-
-
Baptistella, L. H. B., dos Santos, J. F., Ballabio, K. C., and Marsaioli, A. J. Synthesis 1989, 436
-
(1989)
Synthesis
, pp. 436
-
-
Baptistella, L.H.B.1
Dos Santos, J.F.2
Ballabio, K.C.3
Marsaioli, A.J.4
-
28
-
-
78650115694
-
-
3, 400 MHz) of the assumed cyclododeciptycene hexaquinone (red solid) shows three set of signals, δ 7.33 (dd, J = 7.2, 2.8 Hz, 12 H), 7.16 (dd, J = 5.6, 2.8 Hz, 12 H), and 6.04 (s, 12 H) ppm
-
3, 400 MHz) of the assumed cyclododeciptycene hexaquinone (red solid) shows three set of signals, δ 7.33 (dd, J = 7.2, 2.8 Hz, 12 H), 7.16 (dd, J = 5.6, 2.8 Hz, 12 H), and 6.04 (s, 12 H) ppm.
-
-
-
|